LBIS® Mouse MCP-1(CCL-2) ELISA Kit 短时间、微量样品、高灵敏度检测小鼠血清、血浆、尿液中的MCP-1

LBIS® Mouse MCP-1(CCL-2) ELISA Kit
短时间、微量样品、高灵敏度检测小鼠血清、血浆、尿液中的MCP-1

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  • 相关资料
  • Q&A
  • 参考文献

LBIS® Mouse MCP-1(CCL-2) ELISA KitLBIS®  Mouse MCP-1(CCL-2) ELISA Kit                              短时间、微量样品、高灵敏度检测小鼠血清、血浆、尿液中的MCP-1

短时间、微量样品、高灵敏度检测小鼠血清、血浆、尿液中的MCP-1

FUJIFILM Wako Shibayagi的LBIS® 细胞因子 ELISA试剂盒系列新推出Mouse MCP-1试剂盒。针对现有试剂盒因低灵敏度而无法检测正常及低浓度的样品,该试剂盒可实现高灵敏度、高重复性检测。

 


◆关于MCP-1


由125个氨基酸(小鼠)组成的单核细胞诱导蛋白-1(MCP-1)是属于CC趋化因子家族的一种趋化因子,对单核细胞和巨噬细胞有趋化作用。与许多其他趋化因子相同,MCP-1的表达由TNF-α和IL-1等的炎症刺激诱发。MCP-1作为炎症介质,除了单核细胞和巨噬细胞等免疫活性细胞,还从血管内皮细胞、成纤维细胞、管状上皮细胞和平滑肌细胞等大量的细胞中分泌。

由于MCP-1和其受体趋化因子模体受体-2(CCR2)通过动员单核细胞和巨噬细胞到炎症区来延长炎症的时间,所以被认为与慢性炎症性疾病相关。MCP-1通过将炎症巨噬细胞渗入肥胖的脂肪细胞,借助促进炎症来密切参与胰岛素抵抗。基于这些发现,MCP-1在阐明代谢综合征等的分子机制和病理研究中备受关注。

◆特点


● 非卡塔赫纳生物安全议定书对象(不含杆状病毒)

● 微量样品即可检测

● 检测时间短(总反应时间:3 hour 50 min)

● 高精度和高重复性


◆性能

● 样品:小鼠血清、血浆(肝素/EDTA)、尿液

● 样品量:50 μL

● 检测范围:3.85~500 pg/mL (标准曲线范围)

● 同次实验的重复性(5次检测,2个样品):平均C.V.值:小于15%

● 不同次实验的重复性(3次检测,3个样品,4天):平均C.V.值:小于15%

◆数据


标准曲线(例)


LBIS®  Mouse MCP-1(CCL-2) ELISA Kit                              短时间、微量样品、高灵敏度检测小鼠血清、血浆、尿液中的MCP-1



◆试剂盒组成


● 96孔抗体固定化酶标板——1 plate

● 标准品(冻干)——1支

● 缓冲液——60 mL ×1支

● 生物素结合抗体(冻干)——1支

● 过氧化物酶·结合链霉亲和素溶液——100 μL × 1支

● 显色液(TMB)——12 mL × 1支

● 反应终止液——12 mL × 1支

● 浓缩清洗液(10 ×)——100 mL × 1支



◆产品列表


产品编号

厂家编号

产品名称

包装

637-54101

AKMMCP1-011

LBIS Mouse MCP-1 ELISA Kit
LBIS小鼠MCP-1 ELISA试剂盒

96次用

相关产品


LBIS ELISA Kit 细胞因子系列

产品编号

厂家编号

产品名称

包装

小鼠样品检测用

630-44701

AKMIFNG-011

LBIS Mouse IFN-γ ELISA Kit

LBIS小鼠IFN-γ ELISA试剂盒

96次用

638-40841

AKMIL12-011

LBIS Mouse IL-12 ELISA Kit

小鼠IL-12 ELISA试剂盒

96次用

637-44711

AKMIL17-011

LBIS Mouse IL-17A ELISA Kit

LBIS小鼠IL-17A   ELISA试剂盒

96次用

634-44721

AKMTNFA-011

LBIS Mouse TNF-α ELISA Kit

LBIS小鼠TNF-α ELISA试剂盒

96次用

人样品检测用

631-47891

AKH-IFNG

LBIS Human IFN-γ ELISA Kit

LBIS人IFN-γ ELISA试剂盒

96次用

635-42311

AKH-IL6

Human IL-6 ELISA Kit

人IL-6 ELISA试剂盒

96次用

632-42321

AKH-IL8

Human IL-8(CXCL8) ELISA Kit

人IL-8(CXCL8)ELISA试剂盒

96次用

638-53411

AKH-MCP1

LBIS Human MCP-1(CCL2) ELISA Kit

LBIS人MCP-1(CCL2) ELISA试剂盒

96次用

639-42331

AKH-TNFA

Human TNF-α ELISA Kit

人 TNF-αELISA试剂盒

96次用

631-40831

AKH-VEGF

LBIS Human VEGF ELISA Kit

人VEGF ELISA试剂盒

96次用

※ 本页面产品仅供研究用,研究以外不可使用。

LBIS® 血蓝蛋白(KLH)(T细胞依赖性抗原) 大鼠免疫球蛋白M(IgM) ELISA试剂盒 LBIS® KLH(TDAR) Rat-IgM ELISA Kit

LBIS® 血蓝蛋白(KLH)(T细胞依赖性抗原)
大鼠免疫球蛋白M(IgM) ELISA试剂盒
LBIS® KLH(TDAR) Rat-IgM ELISA Kit

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

LBIS® 血蓝蛋白(KLH)(T细胞依赖性抗原)  大鼠免疫球蛋白M(IgM) ELISA试剂盒                              LBIS® KLH(TDAR) Rat-IgM ELISA KitLBIS® 血蓝蛋白(KLH)(T细胞依赖性抗原)

大鼠免疫球蛋白M(IgM) ELISA试剂盒

 


  药品的免疫毒性实验相关方针ICH S8中推荐在无特定免疫毒性标靶情况下进行的T细胞依赖性抗体产生实验(TDAR、T cell Dependent Antibody Reaction)。TDAR被称为T细胞依赖性抗原。例如:通过KLH(Keyhole limpet hemocyanin)的投放对一次抗原刺激而生成IgM性状抗体。接下来进行二次抗原刺激后通过类别转换作用可观察到产生IgG性状抗体。由于本试剂盒可简便测定大鼠血液中IgM性状的抗KLH浓度,所以十分符合上文所述的目的。请与大鼠抗KLH-IgG检测试剂盒配套使用。

◆特点

LBIS® 血蓝蛋白(KLH)(T细胞依赖性抗原)  大鼠免疫球蛋白M(IgM) ELISA试剂盒                              LBIS® KLH(TDAR) Rat-IgM ELISA Kit


● 测定时间短(总反应时间:2小时20分钟)。

● 微量样本即可测定。

● 使用无害的防腐剂。

● 全部试剂为溶液即用类型。

● 高测定精度和高重复性。

 

◆试剂盒组成


组成品

状态

包装

KLH包被96孔板

清洗后使用

96 wells(8×12)/1个

抗KLH大鼠IgM标准溶液(1000 ng/mL)

稀释后使用

200 μL/1瓶

缓冲液

直接使用

100 mL/1瓶

HRP结合抗大鼠IgM抗体

稀释后使用

100 μL/1瓶

显色液(TMB)

直接使用

12 mL/1瓶

终止液(1M H2SO4)※小心轻放

直接使用

12 mL/1瓶

浓缩清洗液(10×)

稀释后使用

100 mL/1瓶

孔板密封膜

3个

产品说明书

1本

 


◆物种交叉性


2000 ng/mL时数据—:无交叉性


动物种类

对象物质

反应性及反应率(%)

大鼠

IgM

100

IgG

IgA

IgE

小鼠

IgG

IgM

IgE

 


◆样本信息


● 大鼠血清·血浆

● 50 μL/well(稀释样本)

※ 用附带的缓冲液将样本稀释至标准曲线范围内。

※ 为了避免非特异反应发生,请将样本稀释200倍以上。

 


测定范围


3.13~200 ng/mL

(标准曲线范围)

 


◆实验数据


精度测试(组内变异)


样本

A

B

1

49.5

164

2

47.7

166

3

48.0

164

4

47.6

161

5

49.7

169

Mean

48.5

165

SD

1.03

2.93

CV(%)

2.1

1.8

单位:ng/mL



重复性测试(组间变异)


测定日/样本

E

F

G

0天

11.1

86.5

187

1天

11.1

86.1

188

2天

11.2

86.3

188

3天

11.1

83.3

186

Mean

11.1

85.6

187

SD

0.0576

1.48

0.814

CV(%)

0.52

1.7

0.44

单位:ng/mL,n=4



加标回收测试


样本C


添加量

实测值

回收量

回收率(%)

0.00

47.3

102

144

96.7

94.8

127

172

125

98.4

140

182

135

96.4

单位:ng/mL,n=2


样本D


添加量

实测值

回收量

回收率(%)

0.00

34.8

16.8

51.9

17.1

102

25.2

59.5

24.7

98.0

42.0

76.7

41.9

99.8

单位:ng/mL,n=2



稀释直线性测试


2个血清样本连续用稀释缓冲液稀释3个梯度测定结果,直线回归值R2=0.9965~0.9998

产品列表
产品编号 产品名称 产品规格 产品等级 备注
633-13769 LBIS® KLH(TDAR) Rat-IgM ELISA Kit
LBIS® 血蓝蛋白(KLH)(T细胞依赖性抗原)大鼠免疫球蛋白M(IgM) ELISA试剂盒
96 tests

LBIS® 小鼠卵清蛋白特异性免疫球蛋白E(OVA-IgE)ELISA试剂盒 LBIS® OVA-IgE Mouse

LBIS® 小鼠卵清蛋白特异性免疫球蛋白E(OVA-IgE)ELISA试剂盒
LBIS® OVA-IgE Mouse

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

LBIS® 小鼠卵清蛋白特异性免疫球蛋白E(OVA-IgE)ELISA试剂盒                              LBIS® OVA-IgE Mouse小鼠卵清蛋白特异性免疫球蛋白E(OVA-IgE) ELISA试剂盒

 


  IgE(Immunoglobulin E,免疫球蛋白E)是第五个被发现的免疫球蛋白,由5个结构域(VH、CHε 1~4)构成的两个Hε链和两个L链中组成的IgE,其分子量约190000,电泳实验中向γ1域移动。IgE的代谢半衰期约3天,正常人血清中的IgE浓度非常低,约300 ng/mL。但在寄生虫感染和枯草热时浓度会升高。与过敏性相关的IgE被称作反应素。因接触过敏原导致反应素含量升高,反应素会在Fc域与存在于皮肤、呼吸道、消化脏器中嗜碱性粒细胞和肥大细胞的FcεR1受体结合,引起细胞过敏。在结合过敏原后细胞发生脱粒现象,组胺,五羟色胺,蛋白酶,肝素,趋化因子,前列腺素,白三烯等被投放,经过支气管收缩和黏膜水肿,分泌亢进,从而诱发支气管哮喘,部分荨麻疹,过敏性鼻炎,过敏性反应等I型过敏性反应。

  本试剂盒是以OVA(卵清蛋白)作为免疫的抗原,在一个简化的反应系统中通过测定鼠抗OVA- IgE抗体值来进行小鼠免疫系统检测的试剂盒。

◆特点

LBIS® 小鼠卵清蛋白特异性免疫球蛋白E(OVA-IgE)ELISA试剂盒                              LBIS® OVA-IgE Mouse


● 测定时间短(总反应时间:1小时50分钟)。

● 微量样本即可测定。

● 使用无害的防腐剂。

● 全部试剂为溶液即用类型。

● 高测定精度和高重复性。

● 操作简便,无需进行特殊前处理。

 

试剂盒组成


组成品

状态

包装

OVA包被96孔板(干燥板)

清洗后使用

96 wells(8×12)/1个

标准溶液(Anti OVA-IgE:1,200 U/mL)(单抗)

稀释后使用

100 μL/1瓶

缓冲液

直接使用

60 mL/1瓶

生物素结合抗小鼠IgE抗体(单抗)

稀释后使用

200 μL/1瓶

过氧化物酶·抗生素结合物

稀释后使用

200 μL/1瓶

显色液(TMB)

直接使用

12 mL/1瓶

终止液(1M H2SO4)※小心轻放

直接使用

12 mL/1瓶

浓缩清洗液(10×)

稀释后使用

100 mL/1瓶

孔板密封膜

3个

产品说明书

1本

 


◆样本信息


● 小鼠血清·血浆

● 10 μL/well(稀释样本)

※ 样本需要用试剂盒附带的缓冲液调至标准曲线范围内。

※ 样本必须稀释10倍以上。

 


测定范围


1.88~120 U/mL(标准曲线范围)

(本试剂盒中1 U/mL定义为抗原结合常数(Ka)为2.0×108 M-1的抗体1.3 ng/mL)

 


实验数据


精度测试(组内变异)


样本

A

B

1

70.7

19.1

2

71.0

18.7

3

77.1

19.6

4

74.3

19.7

5

72.9

18.9

Mean

73.2

19.2

SD

2.6

0.42

CV(%)

3.6

2.2

单位:U/mL



重复性测试(组间变异)


测定日/样本

C

D

E

0天

60.0

15.0

3.75

1天

59.1

15.0

3.75

2天

58.1

14.7

3.65

3天

63.6

16.0

3.48

Mean

60.2

15.2

3.66

SD

2.4

0.57

0.13

CV(%)

4.0

3.7

3.4

单位:U/mL



加标回收测试


样本F


添加量

实测值

回收量

回收率(%)

0.00

6.93

5.35

12.2

5.27

98.5

10.7

17.8

10.9

102

17.1

25.1

18.2

106

单位:U/mL,n=3


样本G


添加量

实测值

回收量

回收率(%)

0.00

40.5

30.8

70.4

29.5

95.8

35.9

77.1

36.6

102

53.9

94.9

54.4

101

单位:U/mL,n=3



稀释直线性测试


2个血清样本连续用稀释缓冲液稀释3个梯度测定结果,直线回归值R2=0.9987~0.9999

参考文献



 1.

Pinocembrin attenuates allergic airway inflammation via inhibition of NF-κB pathway in mice. Gu X, Zhang Q, Du Q, Shen H, Zhu Z. Int Immunopharmacol. 2017 Oct 18;53:90-95.


 2.

A dichloromethane fraction of Triticum aestivum sprouts reduces allergic immune response through inhibiting Th2 differentiation in ovalbumin‑immunized mice. Ki HH, Hwang SW, Lee JH, Kim YH, Kim DK, Lee YM. Mol Med Rep. 2017 Sep;16(3):3535-3541.


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Urban PM2.5 exacerbates allergic inflammation in the murine lung via a TLR2/TLR4/MyD88-signaling pathway. He M, Ichinose T, Yoshida Y, Arashidani K, Yoshida S, Takano H, Sun G, Shibamoto T. Sci Rep. 2017 Sep 8;7(1):11027.


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Activation of group 2 innate lymphoid cells exacerbates and confers corticosteroid resistance to mouse nasal type 2 inflammation. Morikawa T, Fukuoka A, Matsushita K, Yasuda K, Iwasaki N, Akasaki S, Fujieda S, Yoshimoto T. Int Immunol. 2017 May 1;29(5):221-233.


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Aquaporin-3 potentiates allergic airway inflammation in ovalbumin-induced murine asthma. Ikezoe K, Oga T, Honda T, Hara-Chikuma M, Ma X, Tsuruyama T, Uno K, Fuchikami J, Tanizawa K, Handa T, Taguchi Y, Verkman AS, Narumiya S, Mishima M, Chin K. Sci Rep. 2016 May 11;6:25781.


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Exposure to bisphenol A enhanced lung eosinophilia in adult male mice. He M, Ichinose T, Yoshida S, Takano H, Nishikawa M, Shibamoto T, Sun G. Allergy Asthma Clin Immunol. 2016 Apr 14;12:16.


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Differences in allergic inflammatory responses between urban PM2.5 and fine particle derived from desert-dust in murine lungs. He M, Ichinose T, Kobayashi M, Arashidani K, Yoshida S, Nishikawa M, Takano H, Sun G, Shibamoto T. Toxicol Appl Pharmacol. 2016 Apr 15;297:41-55.


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Desert dust induces TLR signaling to trigger Th2-dominant lung allergic inflammation via a MyD88-dependent signaling pathway. He M, Ichinose T, Song Y, Yoshida Y, Bekki K, Arashidani K, Yoshida S, Nishikawa M, Takano H, Shibamoto T, Sun G. Toxicol Appl Pharmacol. 2016 Apr 1;296:61-72.


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Administration of Pigment Epithelium-Derived Factor Inhibits Airway Inflammation and Remodeling in Chronic OVA-Induced Mice via VEGF Suppression. Zha W, Su M, Huang M, Cai J, Du Q. Allergy Asthma Immunol Res. 2016 Mar;8(2):161-9.


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Low-dose benzo[a]pyrene aggravates allergic airway inflammation in mice. Yanagisawa R, Koike E, Win-Shwe TT, Ichinose T, Takano H. J Appl Toxicol. 2016 Feb 25.


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Prevention of allergic rhinitis by ginger and the molecular basis of immunosuppression by 6-gingerol through T cell inactivation. Kawamoto Y, Ueno Y, Nakahashi E, Obayashi M, Sugihara K, Qiao S, Iida M, Kumasaka MY, Yajima I, Goto Y, Ohgami N, Kato M, Takeda K. J Nutr Biochem. 2016 Jan;27:112-22.


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Immunotoxic Effect of Low-Dose Methylmercury Is Negligible in Mouse Models of Ovalbumin or Mite-Induced Th2 Allergy. Nakamura R, Takanezawa Y, Sone Y, Uraguchi S, Sakabe K, Kiyono M.

Biol Pharm Bull. 2016;39(8):1353-8.


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Prevention of allergic rhinitis by ginger and the molecular basis of immunosuppression by 6-gingerol through T cell inactivation. Yoshiyuki Kawamoto, Yuki Ueno, Emiko Nakahashi, Momoko Obayashi, Kento Sugihara, Shanlou Qiao, Machiko Iida, Mayuko Y. Kumasaka, Ichiro Yajima, Yuji Goto, Nobutaka Ohgami, Masashi Kato, Kozue Takeda. The Journal of Nutritional Biochemistry, Volume 27, Jan. 2016, Pages 112–122


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Effects of Sohamhyoong-Tang on Ovalbumin-Induced Allergic Reaction in BALB/c Mice. Jo SH, Lee YJ, Kang DG, Lee HS, Kim DK, Park MC. Evid Based Complement Alternat Med. 2016;2016:6286020.


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Effect of diosmetin on airway remodeling in a murine model of chronic asthma. Ge A, Liu Y, Zeng X, Kong H, Ma Y, Zhang J, Bai F, Huang M. Acta Biochim Biophys Sin (Shanghai). Vol.47(8), p604-11, Aug 2015.


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PM2.5-rich dust collected from the air in Fukuoka, Kyushu, Japan, can exacerbate murine lung eosinophilia. He M, Ichinose T, Ren Y, Song Y, Yoshida Y, Arashidani K, Yoshida S, Nishikawa M, Takano H, Sun G. Inhal Toxicol. Vol.27(6), p287-99, May 2015.


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Anti-asthma potential of crocin and its effect on MAPK signaling pathway in a murine model of allergic airway disease. Xiong Y, Wang J, Yu H, Zhang X, Miao C. Immunopharmacol Immunotoxicol. Vol.10, p1-8, Mar 2015.


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Roles of lipoxin A4 receptor activation and anti-interleukin-1β antibody on the toll-like receptor 2/mycloid differentiation factor 88/nuclear factor-κB pathway in airway inflammation induced by ovalbumin. Kong X, Wu SH, Zhang L, Chen XQ. Mol Med Rep. 2015 Mar 5


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Pharyngeal aspiration of metal oxide nanoparticles showed potential of allergy aggravation effect to inhaled ovalbumin. Horie M, Stowe M, Tabei M, Kuroda E. Inhal Toxicol. Vol.27(3), p181-90, Feb 2015.


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Oxidized dietary oils enhance immediate- and/or delayed-type allergic reactions in BALB/c mice. Ogino H, Sakazaki F, Okuno T, Arakawa T, Ueno H. Allergol Int. Vol.64(1), p66-72, Jan 2015.


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The effects of nodakenin on airway inflammation, hyper-responsiveness and remodeling in a murine model of allergic asthma. Xiong Y, Wang J, Yu H, Zhang X, Miao C, Ma S. Immunopharmacol Immunotoxicol. Vol.36(5), p341-348, Oct 2014.


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Allogeneic pluripotent stem cells suppress airway inflammation in murine model of acute asthma. Ogulur I, Gurhan G, Kombak FE, Filinte D, Barlan I, Akkoc T. International Immunopharmacology, Vol.22(1), p31-40 Sep 2014.


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Effects of prior oral exposure to combinations of environmental immunosuppressive agents on ovalbumin allergen-induced allergic airway inflammation in Balb/c mice. Fukuyama T, Nishino R, Kosaka T, Watanabe Y, Kurosawa Y, Ueda H, Harada T.. Immunopharmacol Immunotoxicol. Vol.36(4), p261-70, Aug 2014.


24.

Enhancement of OVA-induced murine lung eosinophilia by co-exposure to contamination levels of LPS in Asian sand dust and heated dust. Ren Y, Ichinose T, He M, Song Y, Yoshida Y, Yoshida S, Nishikawa M, Takano H, Sun G, Shibamoto T. Allergy, Asthma & Clinical Immunology, Vol.10(1), Jun 2014.


25.

A bacterial extract of OM-85 Broncho-Vaxom prevents allergic rhinitis in mice. Han L, Zheng CP, Sun YQ, Xu G, Wen W, Fu QL. American Journal of Rhinology & Allergy, Vol.28(2), p110-116, Mar-Apr 2014.


26.

Broncho-Vaxom Attenuates Allergic Airway Inflammation by Restoring GSK3β-Related T Regulatory Cell Insufficiency. Fu R, Li J, Zhong H, Yu D, Zeng X, Deng M, Sun Y, Wen W, Li H. PLoS One. 2014 Mar 25;9(3):e92912


27.

Lung inflammation by fungus, Bjerkandera adusta isolated from Asian sand dust (ASD) aerosol and enhancement of ovalbumin-induced lung eosinophilia by ASD and the fungus in mice. Liu B, Ichinose T, He M, Kobayashi F, Maki T, Yoshida S, Yoshida Y, Arashidani K, Takano H, Nishikawa M, Sun G, Shibamoto T. Allergy, Asthma & Clinical Immunology, Vol.10(1), Feb 2014.


28.

Midazolam inhibits IgE production in mice via suppression of class switch recombination. Kusama H, Kobayashi R, Kurita-Ochiai T. Journal of Oral Science, Vol.56(1), p77-83, 2014.


29.

Induction of immune tolerance and reduction of aggravated lung eosinophilia by co-exposure to Asian sand dust and ovalbumin for 14 weeks in mice. He M., Ichinose T., Yoshida S., Takano H., Nishikawa M., Sun G. and Shibamoto T. Allergy, Asthma & Clinical Immunology, Vol.9(19), 2013.


30.

Galangin Abrogates Ovalbumin-Induced Airway Inflammation via Negative Regulation of NF-B. Zha W-J., Qian Y., Shen Y., Du Q., Chen F-F., Wu Z-Z., Li X. and Huang M. Evidence-Based Complementary and Alternative Medicine, Vol.2013 (2013), p14.


31.

Effects of two Asian sand dusts transported from the dust source regions of Inner Mongolia and northeast China on murine lung eosinophilia. M.He, T.Ichinose, Y.Song, Y.Yoshida, K.Arashidani, S.Yoshida, B.Liu, M.Nishikawa, H.Takano, G.Sun. Toxicology and Applied Pharmacology, Available online 26 July 2013.


32.

Effect of the size of receptor in allergy detection using field effect transistor biosensor. S.Hideshima, S.Kuroiwa, M.Kimura, S.Cheng, T.Osaka. Electrochimica Acta, Available online 24 July 2013.


33.

Elevated Macrophage Inflammatory Protein 1α and Interleukin-17 Production in an Experimental Asthma Model Infected with Respiratory Syncytial Virus. T.Ishioka, Y.Yamada, H.Kimura, M.Yoshizumi, H.Tsukagoshi, K.Kozawa, K.Maruyama, Y.Hayashi, M.Kato. Int Arch Allergy Immunol, Vol.161(suppl 2), p129-137, May 2013.


34.

Leukotriene B4 receptor BLT2 negatively regulates allergic airway eosinophilia . Y.Matsunaga, S.Fukuyama, T.Okuno, F.Sasaki, T. Matsunobu, Y.Asai, K.Matsumoto, K.Saeki, M.Oike, Y.Sadamura, K.Machida, Y.Nakanishi, M.Kubo, T.Yokomizo and H.Inoue. The FASEB Journal, Published online before print April 19, 2013.


35.

Effects of exposure to nanoparticle-rich or -depleted diesel exhaust on allergic pathophysiology in the murine lung. Tanaka M., Aoki Y., Takano H., Fujitani Y., Hirano S., Nakamura R., Sone Y., Kiyono M., Ichinose T., Itoh T., Inoue K. Journal of Toxicological Sciences, Vol.38(1), p35-48, Feb 2013.


36.

HIF-1α Inhibition Reduces Nasal Inflammation in a Murine Allergic Rhinitis Model. Zhou H, Chen X, Zhang W-M, Zhu L-P, Cheng L. PLOS one, 2012.


37.

Human Pluripotent Stem Cell-Derived Mesenchymal Stem Cells Prevent Allergic Airway Inflammation in Mice. Sun Y-Q, Deng M-X, He J, Zeng Q-X, Wen W, Wong D S.H, Tse H-F, Xu G, Lian Q, Shi J, Fu Q-L. STEM CELLS, Vol.30(12), p2692-2699, Dec 2012.


38.

Aggravating effects of Asian sand dust on lung eosinophilia in mice immunized beforehand by ovalbumin. He M, Ichinose T, Yoshida S, Takano H, Nishikawa M, Mori I, Sun G, Shibamoto T. Inhalation Toxicology, Vol.24(11) , p751-761, Sep 2012.


39.

Attenuation of airway hyperreactivity and T helper cell type 2 responses by coumarins from Peucedanum praeruptorum Dunn in a murine model of allergic airway inflammation. Xiong Y-Y, Wu F-H, Wang J-S, Li J, Kong L-Y. Journal of Ethnopharmacology, Vol.141(1), p314-321, May 2012.


40.

Effects of lysed Enterococcus faecalis FK-23 on experimental allergic rhinitis in a murine model. Zhu L,Shimada T, Chen R, Lu M, Zhang Q, Lu W, Yin M, Enomoto T, Cheng L. Journal of Biomedical Research, Vol.26(3), p226-234, May 2012.


41.

Sphingosine-kinase 1 and 2 contribute to oral sensitization and effector phase in a mouse model of food allergy. S. C. Diesner., A. Olivera., S. Dillahunt., C. Schultz., T. Watzlawek., E. Forster-Waldl., A. Pollak., E. Jensen-Jarolim., E. Untersmayr., J. Rivera. Immunology Letters, Vol. 141, Issue 2, 30 January 2012, Pages 210-219


42.

Identification of Semaphorin 4B as a Negative Regulator of Basophil-Mediated Immune Responses. Y. Nakagawa., H. Takamatsu., T. Okuno., S. Kang., S. Nojima., T. Kimura., T. R. Kataoka., M. Ikawa., T. Toyofuku., I. Katayama., and A. Kumanogoh. The Journal of Immunology, March 1, 2011 vol. 186 no. 5 2881-2888


43.

Suppression of ovalbumin-induced allergic diarrhea by diminished intestinal peristalsis in RAMP1-deficient mice. R. Yoshikawa., N. Mikami., I. Otani., T. Kishimoto., S. Nishioka., N. Hashimoto., Y. Miyagi., Y. Takuma., K. Sueda., S. Fukada., H. Yamamoto., K. Tsujikawa. Biochemical and Biophysical Research Communications, Vol. 410, Issue 3, 8 July 2011, Pages 389-393


44.

Cortex Mori Radicis extract exerts antiasthmatic effects via enhancement of CD4+CD25+Foxp3+ regulatory T cells and inhibition of Th2 cytokines in a mouse asthma model. H.-J. Kim., H. J. Lee., S.-J. Jeong., H.-J. Lee., S.-H. Kim., E.-J. Park. Journal of Ethnopharmacology, Vol. 138, Issue 1, 31 October 2011, Pages 40-46


45.

Urban particulate matter in Beijin,China,enhances allergen-induced murine lung eosinophilia. He,M.,Ichinose,T.,Yoshida,S.,Nishikawa,M.,Mori,I.,Yanagisawa,R.,Takano,H.,Inoue,K.,Sun,G.,Shibamoto,T. Inhalation Toxicology 22(9):709-718,August,2010


46.

Deficiency in the Serum-Derived Hyaluronan-Associated Protein-Hyaluronan Complex Enhances Airway Hyperresponsiveness in a Murine Model of Asthma. L. Zhu., L. Zhuo., K. Kimata., E. Yamaguchi., H. Watanabe., M. A. Aronica., V. C. Hascall., K. Baba. Int Arch Allergy Immunol 153:223-233 2010


47.

Thioredoxin suppresses airway inflammation independently of systemic Th1/Th2 immune modulation. M. Torii., L. Wang., N. Ma., K. Saito., T. Hori., M. Sato-Ueshima., Y. Koyama., H. Nishikawa., N. Katayama., A. Mizoguchi., H. Shiku., J. Yodoi., K. Kuribayashi., T. Kato. European Journal of Immunology Vol.40(3) 787-796 2010


48.

Peritoneal injection of fucoidan suppresses the increase of plasma IgE induced by OVA-sensitization. Yanase,Y.,Hiragun,T.,Uchida,K.,Ishii,K.,Oomizu,S.,Suzuki,H.,Mihara,S.,Iwamoto,K.,Matsuo,H.,Onishi,N.,Kameyoshi,Y.,and Hide,M. Biochemical and Biophysical Research Communications 387:3:435- 439,2009


49.

Peroxisome Proliferator-Activated Receptor gNegatively Regulates Allergic Rhinitis in Mice. Fukui,N.,Honda,K.,Ito,E.,and Ishikawa K. Allergology Internatioal.58:247-253,2009


50.

IL-16 Variabillity and Modulation by Antiallergic Drugs in a Murine Experimental Allergic Rhinitis Model. Akiyama,K.,Karaki,M.,Kobayshi,R.,Dobashi,H.,Ishida,T, and Mori,N. Allergy and Immunology 149:4,2009


51.

Frequency of Foxp3+CD4+CD25+ T cell is associated with the phenotypes of allergic asthma. Matsumoto,K.,Inoue,H.,Fukuyama,A.,Kan,O,K.,Eguchi,T,M.,Matsumoto,T.,Moriwaki,A.,Nakano,T., and Nakanishi,Y. Respirology 14:2,2009


52.

Differential Regulatory Function of Resting and Preactivated Allergen-Specific CD4+CD25+ Regulatory T Cells in Th2-Type Airway Inflammation. Saito, K., Torii, M., Ning Ma, Tsuchiya, T., Wang, L., Hori, T., Nagakubo, D., Nitta, N.,Kanegasaki, S., Hieshima, K., Yoshie, O., Gabazza, E.C., Katayama, N., Shiku, H.,Kuribayashi, K. and Kato, T. The Journal of Immunology, 181:6889-6897, 2008


53.

Effects of Asian Sand Dust, Arizona Sand Dust, Amorphous Silica and Aluminum Oxide on Allergic Inflammation in the Murine Lung. Ichinose, T., Yoshida, S., Sadakane, K., Takano, H., Yanagizawa, R., Inoue, K., Nishikawa, M.,Mori, I., Kawazato, H., Yasuda, A. and Shibamoto, T. Inhalation Toxicology, Volume 20, Issue 7, 685-694, 2008


54.

The Effects of Microbial Materials Adhered to Asian Sand Dust on Allergic Lung Inflammation. Ichinose,T., Yoshida,S., Hiyoshi,K., Sadakane,K., Takano,H., Nishikawa,M., Mori,I., Yanagisawa,R., Kawazato,H., Yasuda,A., and Shibamoto,T. Arch Environ Contam Toxicol 55:348-357,2008


55.

Differential Regulatory Function of Resting and Preactivated Allergen-Specific CD4+CD25+ Regulatory T cell in Th2-Type Airway Inflammation. Saito,K., Torii,M., Ma,N., Tsuchiya,T., Wang,L.,Hori,T., Nagakubo,D., Nitta,N., Kanegasaki,S., Hieshima,K., Yoshie,O., Gabazza,E,C., Katayama,N., Shiku,H., Kuribayashi,K., and Kato,T. The Journal of Immunology 181:6889-6897,2008


产品列表
产品编号 产品名称 产品规格 产品等级 备注
639-07651 (AKRIE-030)小鼠卵清蛋白特异性免疫球蛋白E(OVA-IgE) ELISA试剂盒
 LBIS® OVA-IgE Mouse
96 tests

LBIS® 大鼠生长激素(GH) ELISA试剂盒 LBIS® Rat GH ELISA Kit

LBIS® 大鼠生长激素(GH) ELISA试剂盒
LBIS® Rat GH ELISA Kit

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LBIS® 大鼠生长激素(GH) ELISA试剂盒                              LBIS® Rat GH ELISA Kit

大鼠生长激素(GH) ELISA试剂盒



  生长激素(Growth hormone,别名Somatotrophic hormone、 STH、 Somatotrop(h)in)主要是由垂体前叶嗜酸性腺垂体分泌的蛋白激素,在大脑和淋巴细胞表达。与GH高度相似的GH2表达于人的胎盘。GH作用于肝脏肌肉肾脏软骨细胞成纤维细胞胸腺上皮细胞。在IGF-1作用下,通过软骨细胞的增殖、硫酸软骨素的合成、肝脏其他器官细胞肥大增殖、促蛋白合成等促进生长,对胸腺细胞分泌胸腺素起到促进作用。GH暂时性表达胰岛素样作用,之后在脂肪细胞中通过脂肪分解增加游离脂肪酸、血糖上升、胰岛素拮抗作用抑制糖分解、肌肉中糖原含量增加、末梢组织胰岛素灵敏性下降等代谢方面起到一定双相性作用。还起到类似催乳素作用对Na、K、Mg、Ca、P的存积促进小肠Ca吸收乳腺发育乳汁分泌等作用。

GHRH生长素释放肽甲状腺激素皮质醇视黄酸均可促进GH合成分泌。另外通过胰高血糖素加压素2-脱氧-D-葡萄糖耐受性精氨酸等酸负载蛋白质摄入TF5β-内啡肽左旋多巴肾上腺素α受体刺激等可促进GH分泌。促进GH分泌的生理状态是低血糖应激(发热,外伤,出血,乙醚麻醉,精神焦虑)空腹运动慢波睡眠等。GH分泌会抑制引起促生长素抑制素(SRIF)活化素肾上腺素β受体刺激葡萄糖游离脂肪酸皮质类固醇投放高浓度IGF-1高浓度GH等现象发生。抑制GH分泌的生理状态是高血糖增加血液中的脂肪异相睡眠等。GH分泌是具有episodic性的。也就是说可间隔性地使血糖浓度急剧上升或下降。因此非人为采血时血中GH水平会变化很大。

◆特点

LBIS® 大鼠生长激素(GH) ELISA试剂盒                              LBIS® Rat GH ELISA Kit

● 测定时间短(总反应时间:5小时)

● 微量样本(标准操作法5 μL)即可测定。

● 使用无害的防腐剂。

● 全部试剂为溶液即用类型。

● 高测定精度和高重复性。

 

试剂盒组成


组成品

状态

包装

抗体包被96孔板

清洗后使用

96 wells(8×12)/1个

标准溶液(20 ng/mL)

稀释后使用

100 μL/1瓶

缓冲液

直接使用

60 mL/1瓶

生物素结合抗GH抗体

稀释后使用

100 μL/1瓶

过氧化物酶·抗生素结合物

稀释后使用

100 μL/1瓶

显色液(TMB)

直接使用

12 mL/1瓶

终止液(1M H2SO4

※小心轻放

直接使用

12 mL/1瓶

浓缩清洗液(10×)

稀释后使用

100 mL/1瓶

孔板密封膜

4个

产品说明书

1本

 


物种交叉性


2000 pg/mL时数据+:有交叉性   ―:无交叉性


动物种类

对象物质

反应性及反应率(%)

大鼠

r-GH

100

Prolactin

0.02

Placental   lactogen

0.02

TSH

LH

FSH

小鼠

GH

TSH

 


◆样本信息


● 大鼠血清·血浆

● 5 μL/well(标准操作法)

※ 样本量可调节范围:5~25 μL。但需用缓冲液将板孔总量调制至50 μL

※ 推荐使用1 mg/mL (终浓度)EDTA作为抗凝剂。

 


◆测定范围


● 31.3~2,000 pg/mL(标准曲线范围)

● 62.6~4,000 pg/mL(样本量25 μL时)

● 0.313~20 ng/mL(标准操作时)

 


◆实验数据


精度测试(组内变异)


样本

A

B

1

262

864

2

247

837

3

250

813

4

258

775

5

251

780

6

257

800

7

254

771

8

270

779

Mean

256

802

SD

7.19

33.5

CV(%)

2.8

4.2

单位:pg/mL



重复性测试(组间变异)


测定日/样本

E

F

G

0天

1626

412

96.0

1天

1576

407

97.9

2天

1615

409

96.1

3天

1561

401

103

Mean

1595

407

98.3

SD

31.0

4.50

3.35

CV(%)

1.9

1.1

3.4

单位:pg/mL,n=4



加标回收测试


样本C


添加量

实测值

回收量

回收率(%)

0.00

101

155

265

164

106

192

285

184

95.8

223

325

224

100

单位:pg/mL,n=2


样本D


添加量

实测值

回收量

回收率(%)

0.00

506

303

822

316

104

466

949

443

95.1

539

1058

552

102

单位:pg/mL,n=2



稀释直线性测试


2个血清样本连续用稀释缓冲液稀释3个梯度测定结果,直线回归值R2=0.999。

参考文献

1.

Daily Fasting Blood Glucose Rhythm in Male Mice: A Role of the Circadian Clock in the Liver. Ando H, Ushijima K, Shimba S, Fujimura A. Endocrinology. 2016 Feb;157(2):463-9.


2.

Casted-immobilization downregulates glucocorticoid receptor expression in rat slow-twitch soleus muscle. Sato S., Suzuki H., Tsujimoto H., Shirato K., Tachiyashiki K., Imaizumia K. Life Sciences, Vol.89(25-26), p962-967, Dec 2011.


3.

Activation of PPARδ promotes mitochondrial energy metabolism and decreases basal insulin secretion in palmitate-treated β-cells. Jiang L., Wan J., Ke L., LU Q., Tong N. Molecular and Cellular Biochemistry, Vol.343(1-2), p249-256, Oct 2010.


4.

The CXCR4 antagonist AMD3100 suppresses hypoxia-mediated growth hormone production in GH3 rat pituitary adenoma cells. Yoshida,D.,Koketshu,K.,Nomura,R.,Teramoto,A. J Neurooncol, 2010.

产品列表
产品编号 产品名称 产品规格 产品等级 备注
639-13749 (AKRGH-010)LBIS® Rat GH ELISA Kit
LBIS® 大鼠生长激素(GH) ELISA试剂盒
96 tests

增加3种产品! 可检测血清血浆样本 LBIS® 试剂盒

增加3种产品! 可检测血清血浆样本 LBIS® 试剂盒

  • 产品特性
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  • Q&A
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增加3种产品! 可检测血清血浆样本 LBIS® 试剂盒增加3种产品!

正常血清/血浆样本也可检测

LBIS® 系列



◆LBIS® Human IL-6 ELISA Kit


  IL-6 是 189 个氨基酸的分泌性糖蛋白,是促进B细胞分化成抗体生成细胞的细胞因子。有研究表示 ,IL-6 与类风湿关节炎的病情有关,其作用在类风湿关节炎等自身免疫性疾病、炎症性疾病领域受到关注。

  本试剂盒能短时间,高灵敏度检测人血清(血浆)中的微量 IL-6。

产品概要

● 标准曲线范围:1.16~500 pg/mL

● 检测时间:总反应时间 3 小时 50 分

● 样本量:100 μL

● 测定波长:主波长 450 nm /副波长 620 nm

● 样本:人血清/血浆(肝素/EDTA)

增加3种产品! 可检测血清血浆样本 LBIS® 试剂盒


〈标准曲线〉

增加3种产品! 可检测血清血浆样本 LBIS® 试剂盒

 


◆LBIS® Human IL-8(CXCL8)ELISA Kit


  IL-8 是通过炎症性细胞因子的刺激在成纤维细胞或单核细胞、血管内皮细胞中产生的 72 或 77 个氨基酸的 2 种类型的炎症性 CXC 趋化因子。IL-8 与多种疾病的相关,并在类风湿关节炎、哮喘等呼吸道疾病、痛风、牙周炎、癌症等研究领域受到了关注。

  本试剂盒能短时间,高灵敏度检测人血清(血浆)中的微量 IL-8。

产品概要

● 标准曲线范围:0.686~500 pg/mL

● 检测时间:总反应时间 3 小时 50 分

● 样本量:100 μL

● 测定波长:主波长 450 nm / 副波长 620 nm

● 样本:人血清/血浆(肝素/EDTA)


〈标准曲线〉

增加3种产品! 可检测血清血浆样本 LBIS® 试剂盒

 


◆LBIS® Human TNF-α ELISA Kit


  TNF-α 是能引起移植到小鼠中的肿瘤发生出血性坏死的诱导因子,是由 157 个氨基酸组成的炎症性细胞因子。TNF-α 与多种疾病相关,在类风湿关节炎、炎症、糖尿病・高血脂、肾病、白血病、骨质疏松等领域受到关注。

  本试剂盒能短时间,高灵敏度检测人血清(血浆)中的微量 TNF-α。


产品概要

● 标准曲线范围:2.05~500 pg/mL

● 检测时间:总反应时间 3 小时 50 分

● 样本量:100 μL

● 测定波长:主波长 450 nm / 副波长 620 nm

● 样本:人血清/血浆(肝素/EDTA)


〈标准曲线〉

增加3种产品! 可检测血清血浆样本 LBIS® 试剂盒



欲了解相关信息请点击文字:

新产品 人IL-6/IL-8/TNF-α ELISA试剂盒发售通知

Lbis® 疾病相关动物模型ELISA试剂盒系列

产品列表
产品编号 产品名称 产品规格 产品等级 备注
635-42311 人IL-6 ELISA试剂盒,AKH-IL6
LBIS®  Human IL-6 ELISA Kit
96次
632-42321 人IL-8(CXCL8) ELISA试剂盒,AKH-IL8
LBIS®  Human IL-8(CXCL8) ELISA Kit
96次
639-42331 人 TNF-α ELISA试剂盒,AKH-TNFA
LBIS®  Human TNF-α ELISA Kit
96次

LBIS® 小鼠/大鼠 高分子量脂联素 ELISA 试剂盒 LBIS® High Molecular Adiponectin-Mouse/Rat

LBIS® 小鼠/大鼠 高分子量脂联素 ELISA 试剂盒
LBIS® High Molecular Adiponectin-Mouse/Rat

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LBIS® High Molecular Adiponectin-Mouse/RatLBIS® 小鼠/大鼠 高分子量脂联素 ELISA 试剂盒                              LBIS® High Molecular Adiponectin-Mouse/Rat

LBIS® 小鼠/大鼠 高分子量脂联素 ELISA 试剂盒

LBIS® 小鼠/大鼠 高分子量脂联素 ELISA 试剂盒                              LBIS® High Molecular Adiponectin-Mouse/Rat


Adiponectin(脂联素)是脂肪细胞分泌的一种细胞因子。作为脂肪细胞因子,控制脂肪代谢和胰岛素感受性、是抗糖尿病、抗动脉粥样硬化、抗炎症的重要物质。血液中的脂联素通过聚集单聚体形成3聚体、6聚体或者是 12-18 聚体。三聚体(LMW)通过胶原三螺旋链的非共价相互作用以及球状体 C1q 域的疏水相互作用形成。三聚体聚集形成六聚体(MMW)或者更大的多聚体(HMW)。

Adiponectin 与各种各样的生长因子相结合有明显的亲和性,将其隔离能影响细胞的生长、血管新生和细胞组织的重建。血液中 HMW 的测定值除了表示总脂联素以外,同时明确地反映出 BMI 和性别、体重减轻的影响、糖耐量、肝脏的胰岛素感受性、代谢综合征和2型糖尿病。预计 HMW 的测定比起总脂联素的测定,对于代谢综合征和 DM2 的分析更有帮助。

LBIS® 的此款试剂盒只用于测定高分子 Adiponectin。

◆特点

 

● 短时间测定(总的反应时间:4小时)

● 微量样品可测

● 使用对环境无害的防腐剂

● 全部试剂均为液体,可直接使用

● 精密的测定精度和高再现性

 

 

◆构成

 

组成部分

状态

容量

(A)   抗体固相化 96 孔板

洗净后使用

96 wells(8×12)/1块

(B)   标准溶液(2,000 ng/mL)

稀释后使用

200 μL/1 瓶

(C)   缓冲液

即用

60 mL/1 瓶

(D)   HRP标识抗脂联素抗体

稀释后使用

100 μL/1 瓶

(F)   显色液(TMB)

即用

12 mL/1 瓶

(H)   反应终止液(1M H2SO4)※小心轻放

即用

12 mL/1 瓶

( I ) 浓缩洗净液(10×)

稀释后使用

100 mL/1 瓶

封板膜

3 张

使用说明书

1 份

◆交叉反应

动物种类

对象物质

反应性和交叉率(%)

Mouse

Adiponectin(HMW)

100

Adiponectin(Hexamer)

<5

Adiponectin(Trimer)

不存在交叉反应

Adiponectin(Monomer)

不存在交叉反应

MCH

不存在交叉反应

TNF-α

不存在交叉反应

IFN-γ

不存在交叉反应

Insulin

不存在交叉反应

Leptin

不存在交叉反应

Rat

Adiponectin(HMW)

100

Adiponectin(Monomer)

不存在交叉反应

TNF-α

不存在交叉反应

IFN-γ

不存在交叉反应

Insulin

不存在交叉反应

Leptin

不存在交叉反应

※交叉率浓度为1,000 ng/mL

◆样品信息

小鼠/大鼠的血清•血浆•培养液

50 μL/well(稀释样品)

※血浆采血建议使用肝素处理

※正常样品的稀释倍数为50倍(~25倍)

 

◆测量范围

3.13~200 ng/mL(标准曲线范围)

78.25~5,000 ng/mL(25倍稀释样品)

0.1565~10 μg/mL(50倍稀释样品)

 

◆Validation data

精度测试(组内变异)

样品

A

B

1

29.5

129

2

30.7

125

3

29.8

128

4

29.0

126

5

29.6

126

mean

29.7

127

SD

0.631

1.89

CV(%)

2.12

1.49

单位:ng/mL

重复性测试(组间变异)

测量日/样品

C

D

E

第0天

196

126

62.5

第1天

192

130

59.1

第2天

196

125

60.7

第3天

190

125

60.3

mean

193

127

60.7

SD

2.63

2.27

1.41

CV(%)

1.36

1.79

2.33

单位:ng/mL n=2

加标回收测试

样品H

添加量

实测值

回收量

回收率(%)

0

68.5

35.0

103

34.5

98.6

65.0

132

63.5

97.7

95.0

165

96.9

102

单位:ng/mL n=2



样品I

添加量

实测值

回收量

回收率(%)

0

23.3

18.0

40.3

17.0

94.4

26.0

50.6

27.3

105

32.0

55.5

32.2

101

单位:ng/mL n=2

 

稀释直线性测试

用稀释缓冲液分3次连续稀释2个血清样品的测量结果,直线回归方程的 R在 0.9987~0.9993 之间。

相关资料


LBIS® 小鼠/大鼠 高分子量脂联素 ELISA 试剂盒                              LBIS® High Molecular Adiponectin-Mouse/Rat LBIS® 小鼠/大鼠 高分子量脂联素 ELISA 试剂盒                              LBIS® High Molecular Adiponectin-Mouse/Rat LBIS® 小鼠/大鼠 高分子量脂联素 ELISA 试剂盒                              LBIS® High Molecular Adiponectin-Mouse/Rat
说明书

ELISA试剂盒选择指南①②

ELISA试剂盒选择指③④

参考文献



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21.

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25.

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26.

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27.

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28.

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29.

The novel dipeptidyl peptidase-4 inhibitor teneligliptin prevents high-fat diet-induced obesity accompanied with increased energy expenditure in mice. Fukuda-Tsuru S., Kakimoto T., Utsumi H., Kiuchi S., Ishi S. European Journal of Pharmacology, Vol.723(15), p207-215, Jan 2014.


30.

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32.

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33.

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34.

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35.

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36.

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37.

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38.

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39.

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40.

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42.

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49.

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产品列表
产品编号 产品名称 产品规格 产品等级 备注
638-13079 (AKMAN-011)LBIS® Mouse/Rat HMW Adiponectin ELISA Kit
LBIS® 小鼠/大鼠 高分子量脂联素 ELISA试剂盒
96 tests

LBIS® 小鼠瘦素 ELISA 试剂盒 LBIS® Leptin-Mouse

LBIS® 小鼠瘦素 ELISA 试剂盒
LBIS® Leptin-Mouse

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

LBIS® Leptin-MouseLBIS® 小鼠瘦素 ELISA 试剂盒                              LBIS® Leptin-Mouse

LBIS® 小鼠瘦素 ELISA 试剂盒

  瘦素(Leptin)是一种分子量为16KD的蛋白质类激素。主要由白色脂肪组织产生,其它组织如褐色脂肪组织、胎盘、卵巢、骨骼肌、胃底部、乳腺上皮细胞、骨髓、下垂体、肝脏等也能检测到。其在大鼠和小鼠中有97%的同源性。瘦素在突变种肥胖小鼠中发现,是通过调节食欲和新陈代谢来参与至能量平衡的一种重要的激素。血液中瘦素的浓度会因为空腹和低热量饮食而降低,但进食后并不会有明显增加,只有肥胖即脂肪组织量增大的情况下才会增加,可反映身体脂肪量。瘦素进入大脑,通过抑制体内下丘脑神经肽Y(NPY)和刺鼠基因相关蛋白(AgRP)表达神经的受体,另外活化体内 α-MSH 表达神经,起到降低食欲,减少进食的作用。但是,对于严重肥胖的人,虽然他们血液中瘦素的浓度很高,但对瘦素有抗性,瘦素并不能发挥抑制食欲的作用。全身性脂肪萎缩病引起的瘦素降低或缺乏,会造成胰岛素抗性、糖尿病、脂肪肝、高甘油三酯血症等疾病。除此之外,瘦素也被认为与对动脉粥样硬化的免疫反应、能量平衡和性周期相关,与肺泡表面活性剂的产生也有关系。

◆特点

 • 短时间测定(总的反应时间:3小时)

 • 微量样品(标准操作:10 μL)可测

 • 使用对环境无害的防腐剂

 • 全部试剂均为液体,可直接使用

 • 精密的测定精度和高再现性

◆构成

 

组成

状态

容量

(A)抗体固相化 96 孔板(干燥孔板)

洗净后使用

96 wells(8×12)/1 块

(B)瘦素标准溶液(小鼠)(5,000 pg/mL)

稀释后使用

500 μL/1 瓶

(C)缓冲液

即用

60 mL/1 瓶

(D)生物素结合抗瘦素抗体

稀释后使用

200 μL/1 瓶

(E)过氧化物・抗生物素蛋白结合物

稀释后使用

200 μL/1 瓶

(F)显色液(TMB)

即用

12 mL/1 瓶

(H)反应终止液(1M H2SO4)※小心轻放

即用

12 mL/1 瓶

( I )浓缩洗净液(10×)

稀释后使用

100 mL/1 瓶

封板膜

3 张

使用说明书

1 份

◆交叉反应

 ※交叉反应是浓度为 3,000 pg/m时的数据

动物种类

对象物质

反应性和反应率(%)

Mouse

Leptin

100

α-MSH

IFN-γ

MCH

TNF-α

Rat

Leptin

31.5

Human

Lepin

+:存在交叉反应

―:不存在交叉反应

◆样品信息

小鼠的血清、血浆

10 μL/well(标准操作)

※样品量在10~50 μL范围内可以配制

 

◆测量范围

20.6~5,000 pg/mL(样品量50 μL

103~25,000 pg/mL(样品量10 μL

◆Validation data

精度测试(组内变异)

样品

A

B

C

1

3818

846

405

2

3810

856

405

3

3979

842

394

4

4047

851

392

5

4046

856

420

mean

3940

850

403

SD

118

6.18

11.2

CV(%)

3.0

0.73

2.8

单位:pg/mL

重复性测试(组间变异)

测量日/样品

D

E

第0天

5007

1052

第1天

5126

1063

第2天

5069

1027

第3天

5000

1000

mean

5051

1035

SD

59.3

28.0

CV(%)

1.2

2.7

单位:pg/mL n=2

加标回收测试

样品F

添加量

实测值

回收量

回收率(%)

0.00

994.9

337

1334.0

339.1

101

1061

2099.0

1104

104

1238

2284.0

1289

104

单位:pg/mL n=2

样品G

添加量

实测值

回收量

回收率(%)

0.00

1996

2731

4741

2745

101

4682

6444

4448

95.0

5462

7717

5721

105

单位:pg/mL n=2

稀释直线性测试

用稀释缓冲液分5次连续稀释2个血清样品的测量结果,线性回归方程的R2在0.9992~0.9997之间。

欲了解更多相关产品信息,请点击文字:LBIS® 疾病相关动物模型ELISA试剂盒系列


相关资料


LBIS® 小鼠瘦素 ELISA 试剂盒                              LBIS® Leptin-Mouse LBIS® 小鼠瘦素 ELISA 试剂盒                              LBIS® Leptin-Mouse LBIS® 小鼠瘦素 ELISA 试剂盒                              LBIS® Leptin-Mouse
说明书

ELISA试剂盒选择指南①②

ELISA试剂盒选择指③④

参考文献



 1.

Inhibition of Gastric Inhibitory Polypeptide Receptor Signaling in Adipose Tissue Reduces Insulin Resistance and Hepatic Steatosis in High-Fat Diet-Fed Mice. Joo E, Harada N, Yamane S, Fukushima T, Taura D, Iwasaki K, Sankoda A, Shibue K, Harada T, Suzuki K, Hamasaki A, Inagaki N. Diabetes. 2017 Apr;66(4):868-879 


 2.

DNA Methylation Suppresses Leptin Gene in 3T3-L1 Adipocytes. Kuroda M, Tominaga A, Nakagawa K, Nishiguchi M, Sebe M, Miyatake Y, Kitamura T, Tsutsumi R, Harada N, Nakaya Y, Sakaue H. PLoS One. 2016 Aug 5;11(8):e0160532.


 3.

Sodium alginate prevents progression of non-alcoholic steatohepatitis and liver carcinogenesis in obese and diabetic mice. Miyazaki T, Shirakami Y, Kubota M, Ideta T, Kochi T, Sakai H, Tanaka T, Moriwaki H, Shimizu M. Oncotarget. 2016 Mar 1;7(9):10448-58.


 4.

Comparison of two Kampo medicines in a diet-induced mouse obesity model. Fengying Gao, Satoru Yokoyama, Makoto Fujimoto, Koichi Tsuneyama, Ikuo Saiki, Yutaka Shimada andYoshihiro Hayakawa. Traditional & Kampo Medicine, Volume 2, Issue 2, pages 60–66, September 2015


 5.

Effect of Keishibukuryogan on Genetic and Dietary Obesity Models. Fengying Gao, Satoru Yokoyama, Makoto Fujimoto, Koichi Tsuneyama, Ikuo Saiki, Yutaka Shimada, and Yoshihiro Hayakawa. Evid Based Complement Alternat Med. 2015; 2015: 801291.


 6.

Overexpression of the adiponectin gene mimics the metabolic and stress resistance effects of calorie restriction, but not the anti-tumor effect. Kamohara R, Yamaza H, Tsuchiya T, Komatsu T, Park S, Hayashi H, Chiba T, Mori R, Otabe S, Yamada K, Nagayasu T, Shimokawa I. Exp Gerontol. 2015 Apr;64:46-54.


 7.

Preventive effects of astaxanthin on diethylnitrosamine-induced liver tumorigenesis in C57/BL/KsJ-db/db obese mice. Ohno T, Shimizu M, Shirakami Y, Miyazaki T, Ideta T, Kochi T, Kubota M, Sakai H, Tanaka T, Moriwaki H. Hepatol Res. Jul 2015.


 8.

Sudachitin, a polymethoxylated flavone, improves glucose and lipid metabolism by increasing mitochondrial biogenesis in skeletal muscle. Tsutsumi R, Yoshida T, Nii Y, Okahisa N, Iwata S,Tsukayama M, Hashimoto R, Taniguchi Y, Sakaue H, Hosaka T, Shuto E, Sakai T. 

Nutrition & Metabolism, 11:32, Jul 2014.


 9.

Type 2 diabetic conditions in Otsuka Long-Evans Tokushima Fatty rats are ameliorated by 5-aminolevulinic acid. Sato T, Yasuzawa T, Uesaka A, Izumi Y, Kamiya A, Tsuchiya K, Kobayashi Y, Kuwahata M, Kido Y. Nutr Res. Vol.34(6), p544-551, Jun 2014.


10.

Inhibitory Effects of Japanese Herbal Medicines Sho-saiko-to and Juzen-taiho-to on Nonalcoholic Steatohepatitis in Mice. Takahashi Y, Soejima Y, Kumagai A, Watanabe M, Uozaki H, Fukusato T. PLoS One. 2014 Jan 22;9(1):e87279.


11.

Down-Regulation of Hepatic Stearoyl-CoA Desaturase-1 Expression by Fucoxanthin via Leptin Signaling in Diabetic/Obese KK-A y Mice. Beppu F., Hosokawa M., Yim M-J., Shinoda T., Miyashita K. Lipids, Vol.48(5), p449-455, May 2013.


12.

Dietary Combination of Fish Oil and Taurine Decreases Fat Accumulation and Ameliorates Blood Glucose Levels in Type 2 Diabetic/Obese KK-Ay Mice. N. Mikami., M. Hosokawa., K. Miyashita. Journal of Food Science, Vol. 77(6), pH114-H120, Jun 2012.


13.

Effects of Gametophytes of Ecklonia Kurome on the Levels of Glucose and Triacylglycerol in db/db, Prediabetic C57BL/6J and IFN-γ KO Mice. F. Dwiranti., M. Hiraoka., T. Taguchi., Y. Konishi., M. Tominaga., A. Tominaga. Int J B 64 iomed Sci, Vol.8, No.1, Mar 2012.


14.

Overexpression of FoxO1 in the Hypothalamus and Pancreas Causes Obesity and Glucose Intolerance. H.-J. Kim., M. Kobayashi., T. Sasaki., O. Kikuchi., K. Amano., T. Kitazumi., Y.-S. Lee., H. Yokota-Hashimoto., V. Y. Susanti., Y. Ido Kitamura., J. Nakae., and T. Kitamura. Endocrinology, Vol.153, No.2, p659-671, Feb 2012.


15.

Spirulina improves non-alcoholic steatohepatitis, visceral fat macrophage aggregation, and serum leptin in a mouse model of metabolic syndrome. M. Fujimoto., K. Tsuneyama., T. Fujimoto., C. Selmid., 

M. E. Gershwin., Y. Shimada. Digestive and Liver Disease, 2012.


16.

Prevention mechanisms of glucose intolerance and obesity by cacao liquor procyanidin extract in high-fat diet-fed C57BL/6 mice. Y. Yamashita., M. Okabe., M. Natsume., H. Ashida. Archives of 

Biochemistry and Biophysics, 2012.


17.

Preventive Effects of Curcumin on the Development of Azoxymethane-Induced Colonic Preneoplastic Lesions in Male C57BL/KsJ-db/db Obese Mice. M. Kubota., M. Shimizu., H. Sakai., Y. Yasuda., D. Terakura., A. Baba., T. Ohno., H. Tsurumi., T. Tanaka., H. Moriwaki. Nutrition and Cancer, Vol. 64(1), 2012.


18.

Caffeic Acid Phenethyl Ester Suppresses the Production of Adipocytokines, Leptin, Tumor Necrosis Factor -Alpha and Resistin, during Differentiation to Adipocytes in 3T3-L1 Cells. S, Juman., N, Yasui., H, Okuda., A,Ueda., H, Negishi., T, Miki. and K, Ikeda. Biological and Pharmaceutical Bulletin Vol. 34 (2011) , No.4, 490.


19.

Mate Tea(Ilex paraguariensis)Promotes Satiety and Body Weight Lowering in Mice:Involvement of Glucagon-Like Peptide-1. G, M, E, Hussein., H, Matsuda., S, Nakamura., M, Hamao., T, Akiyama., K, Tamura., and M, Yoshikawa. Biol.Pharm.Bull. Vol.34(12), p1849-1855, 2011.


产品列表
产品编号 产品名称 产品规格 产品等级 备注
631-10389  (AKRLP-011)LBIS® Mouse Leptin ELISA kit
LBIS®小鼠瘦素 ELISA试剂盒 
96 tests

LBIS® 小鼠 C-肽 ELISA 试剂盒(U型) LBIS® C-Peptide-Mouse (U type)

LBIS® 小鼠 C-肽 ELISA 试剂盒(U型)
LBIS® C-Peptide-Mouse (U type)

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

LBIS® C-Peptide-Mouse (U type)LBIS® 小鼠 C-肽 ELISA 试剂盒(U型)                              LBIS® C-Peptide-Mouse (U type)

LBIS® 小鼠 C-肽 ELISA 试剂盒(U 型)

  胰岛素是细胞中的单链胰岛素原合成后,形成二硫键,通过酶分解激活,裂解成肽与胰岛素。小鼠、大鼠的胰岛素的氨基酸序列相同,但肽部分稍有不同。小鼠C肽1是 29 个氨基酸,2是 31 个的单链肽。肽是从胰岛素原分离后,与胰岛素一同分泌生成的。长期以来,人们一直认为肽没有生物活性,仅在合成胰岛素过程中,保证A链和B链正确折叠以及二硫键正确配对时起作用。近年,随着研究的不断深入,证明了肽具有多种生物学作用。首先,10-9M 的肽能与内皮细胞、肾小管上皮细胞和成纤维细胞表面的G蛋白偶联受体结合。激活细胞中钙离子依赖性的信号、激活 Na-K-ATPase、促进内皮细胞的 NO 合成、与受体的结合有立体结构特异性;与胰岛素、胰岛素原、IGF-I、-II、NPY 之间无交叉反应。而且通过对缺少肽的Ⅰ型糖尿病患者注射肽类药物,能起到增强骨骼肌以及皮肤的血液循环、降低肾小球超滤的风险、抑制白蛋白从尿液中的排泄、改善神经机能的作用。但对身体健康的人来说,这类药物没有此等功效。因此,建议Ⅰ型糖尿病患者可以在注射胰岛素的同时,投放肽,有利于防止并发症的发生。

  肽的末端的五肽(27-31)在与受体的结合中起着重要的作用,缺少这部分的 Des(27-31)肽就会失去它的作用。这种五肽可以完全取代肽和受体的结合,激活 Na+-K+ATPase。有报告指出新生大鼠中 Des(27-31)肽的存在量约占肽总量的37%,而在成年大鼠中只占8.5%。

  肽在血液中的寿命是胰岛素的好几倍。在临床上,可以通过测量肽在血液中的浓度来观察胰岛素的合成和分泌功能。且肽在尿液中多量排除,一定程度上与血液中肽的平均值相关,所以也可以通过尿液来检测。

  作为人工胰岛中胰岛素分泌的指标,肽测量是有效的。由于在培养液中经常添加胰岛素,如果要测量培养后培养液中的胰岛素的话,就不能很好地区别出分泌的胰岛素和添加的胰岛素,必须减掉培养开始时胰岛素的量。这种情况下,如果分泌的胰岛素量过少,测量误差的影响会增大,从而不能做出正确的判断。这时候,如果测量肽,因为肽与胰岛素是等摩尔分泌的,所以能够正确判断分泌的胰岛素。

  本公司的整套产品能够识别肽1、2的交叉部分,可以测量肽的总量。

◆特点

● 短时间测定(完全反应时间:5小时)

● (标准用量 10 μL)可测

● 使用对环境无害的防腐剂

● 全部试剂均为液体,可直接使用

● 精密的测定密度和高再现性

◆构成

组成

状态

容量

(A) 抗体固相化   96 孔板

洗净后使用

96 wells(8×12)/1 块

(B) 标准溶液(6,000 pg/mL)

稀释后使用

500 μL/1 瓶

(C) 缓冲液

即用

60 mL/1 瓶

(D) 抗C-肽抗体生物素结合

稀释后使用

100 μL/1 瓶

(E) 过氧化物・抗生物素蛋白结合物

稀释后使用

100 μL/1 瓶

(F) 显色液(TMB)

即用

12 mL/1 瓶

(H) 反应停止液(1M   H2SO4)※小心轻放

即用

12 mL/1 瓶

( I ) 浓缩洗净液(10×)

稀释后使用

100 mL/1 瓶

封板膜

4 张

使用说明书

1 份

◆样本

小鼠的血清或血浆

10 μL/well(用本品配备的缓冲液稀释后、50 μ分注在孔板中。)

◆测定范围

46.9~3,000 pg/mL(标准曲线范围)

234.5~15,000 pg/mL(检体量 10 μL 的时候)

◆Validation data

 

精度测试(组内变异)

 

样本

A

B

1

976

238

2

969

230

3

965

230

4

1023

235

5

977

231

6

1018

228

7

1038

229

8

995

225

mean

995

231

SD

27.7

4.10

CV(%)

2.78

1.78

单位:pg/mL

重复性测试(组间变异)

 

测量日/检体

C

D

E

第0天

1502

301

60.9

第1天

1500

302

63.8

第2天

1499

301

62.2

第3天

1501

300

58.8

mean

1500

301

61.4

SD

1.12

0.66

2.13

CV(%)

0.07

0.22

3.46

单位:pg/mL, n=4

加标回收测试

 

样本F

添加量

实测值

回收量

回收率(%)

0.00

300

265

551

250

94

398

683

382

96

531

827

527

99

单位:pg/mL, n=2

样本G

添加量

实测值

回收量

回收率(%)

0.00

58.2

28.9

86.7

28.5

99

38.6

98.2

40.0

104

77.4

139

80.8

104

单位:pg/mL, n=2

稀释直线性测试

用稀释缓冲液分三次连续稀释2个血清检体的结果,直线回归方程的 R是 1.00 。

欲了解更多相关产品信息,请点击文字:LBIS® 疾病相关动物模型ELISA试剂盒系列


相关资料


LBIS® 小鼠 C-肽 ELISA 试剂盒(U型)                              LBIS® C-Peptide-Mouse (U type) LBIS® 小鼠 C-肽 ELISA 试剂盒(U型)                              LBIS® C-Peptide-Mouse (U type) LBIS® 小鼠 C-肽 ELISA 试剂盒(U型)                              LBIS® C-Peptide-Mouse (U type)
说明书

ELISA试剂盒选择指南①②

ELISA试剂盒选择指③④

参考文献


 1.

Inhibition of Gastric Inhibitory Polypeptide Receptor Signaling in Adipose Tissue Reduces Insulin Resistance and Hepatic Steatosis in High-Fat Diet-Fed Mice. Joo E, Harada N, Yamane S, Fukushima T, Taura D, Iwasaki K, Sankoda A, Shibue K, Harada T, Suzuki K, Hamasaki A, Inagaki N. Diabetes. 2017 Apr;66(4):868-879.


 2.

Inhibition of Gastric Inhibitory Polypeptide Receptor Signaling in Adipose Tissue Reduces Insulin

Resistance and Hepatic Steatosis in High Fat Diet-Fed Mice. Joo E, Harada N, Yamane S, Fukushima

T, Taura D, Iwasaki K, Sankoda A, Shibue K, Harada T, Suzuki K, Hamasaki A, Inagaki N. Diabetes.

2017 Jan 17.


 3.

Insulin Release from the Beta Cells in Acatalasemic Mice Is Highly Susceptible to Alloxan-Induced Oxidative Stress. Kazunori Takemoto, Wakana Doi, Ken Kataoka, Kohji Ishihara, Da-Hong Wang, Hitoshi Sugiyama, Noriyoshi Masuoka. Journal of Diabetes Mellitus, 2015, 5, 81-89


 4.

Effect of Burdock Root and the Fermented Product on Alloxan-Induced Mouse Hyperglycemia

Wakana Doi, Yumi Asada, Ayaka Ohno, Yoshiko Okuda, Shota Masuda, Ayano Matsumoto,

Chihiro Mori, Takaya Agarie, Kohji Ishihara, Takayuki Murakami & Noriyoshi Masuoka Journal of

Food Research; Vol. 4, No. 4; 201


 5.

Tissue Complex of Adult Pancreatic Duct and Vascular Endothelial Cells Promotes In Vitro Differentiation into Insulin-Producing Cells. Jun Kanamune, Chongmun Kim, Yasuhiro Iwanaga, Jorge David Rivas-Carrillo, Shoichiro Sumi, Shinji Uemoto and Kazuyuki Yokokawa. J Stem Cell Res Dev 2015, 2: 005


 6.

Anti-diabetic effect of purple corn extract on C57BL/KsJ db/db mice. Bo Huang, Zhiqiang Wang, Jong Hyuk Park, Ok Hyun Ryu, Moon Ki Choi, Jae-Yong Lee, Young-Hee Kang, and Soon Sung Lim. Nutr Res Pract. 2015 Feb;9(1):22-29.


 7.

Xanthohumol Improves Diet-induced Obesity and Fatty Liver by Suppressing Sterol Regulatory Element-binding Protein (SREBP) Activation. Miyata S, Inoue J, Shimizu M, Sato R. J Biol Chem. 2015 Aug 14;290(33):20565-79.


 8.

Effect of Aspergillus awamori-Fermented Burdock Root on Mouse Diabetes Induced by

Alloxan—Prevention of Cell Apoptosis. Kazunori Takemoto, Wakana Doi, Ayumi Zukeran, Junji Inoue, Kohji Ishihara, Noriyoshi Masuoka. Food and Nutrition Sciences, Vol.5 No.16(2014), Article ID:49228,7 pages


 9.

Engineering of pseudoislets: effect on insulin secretion activity by cell number, cell population, and microchannel networks. Kojima N, Takeuchi S, Sakai Y. Transplant Proc. Vol.46(4), p1161-65, May 2014.


10.

Evaluation of 7-O-galloyl-d-sedoheptulose, isolated from Corni Fructus, in the adipose tissue of type 2 diabetic db/db mice. Park CH., Tanaka T., Yokozawa T. Fitoterapia, Vol.89, p131-142, Sep 2013.


11.

Periaortic adipose tissue-specific activation of the renin-angiotensin system contributes to atherosclerosis development in uninephrectomized apoE-/- mice. Kawahito H., Yamada H., Irie D., Kato T., Akakabe Y., Kishida S., Takata H., Wakana N., Ogata T., Ikeda K., Ueyama T., Matoba S., Mori Y., Matsubara H. American Journal of Physiology – Heart and Circulatory Physiology, Vol.305, p667-675, Sep 2013.


12.

Effect of vitamin E on alloxan-induced mouse diabetes. Kamimura W., Doi W., Takemoto K., Ishihara K., Wang D-H., Sugiyama H., Oda S., Masuoka N. Clinical Biochemistry, Vol.46(9), p795-798, Jun 2013.


13.

Evaluation of 7-O-galloyl-d-sedoheptulose, isolated from Corni Fructus, in the adipose tissue of type 2 diabetic db/db mice. C.H.Park, T.Tanaka, T.Yokozawa. Fitoterapia,  Vol.89, p131-42, Sep 2013.


14.

Therapeutic approach for type 1 diabetes mellitus using the novel immunomodulator FTY720 (fingolimod) in combination with once-daily injection of insulin glargine in non-obese diabetic mice. T.Tsuji, M.Inoue, Y.Yoshida, T.Fujita, Y.Kaino, T.Kohno. Journal of Diabetes Investigation, Vol.3(2), p132-137, Apr 2012.


15.

Effect of vitamin E on alloxan-induced mouse diabetes. Kamimura W, Doi W, Takemoto K, Ishihara K, Wang D-H, Sugiyama H, Oda S, Masuoka N. Clinical Biochemistry, Mar 2013.


16.

Intramedullary Cavity as an Implant Site for Bioartificial Pancreas: An In Vivo Study on Diabetic Canine. Y, Kai-Chiang., W, Chang-Chin., S, Shoichiro., K, Tzong-Fu., L, Sheng-Chuan., L, Feng-Huei. Transplantation, Vol. 90(6), p604-611, Sep 2010.


17.

The in vivo performance of bioartificial pancreas in bone marrow cavity: A case report of a spontaneous diabetic feline. K, C, Yang., C, C, Wu., S, C, Lin., S, Sumi., F, H, Lin. Biochemical and Biophysical Research Communications, Vol.393(3), p362-364, Mar 2010.


18.

In vitro reprogramming of adult hepatocytes into insulin-producing cells without viral vectors . H, Motoyama., S, Ogawa., A, Kubo., S, Miwa., J, Nakayama., Y, Tagawa., S, Miyagawa. Biochemical and Biophysical Research Communications, Vol.385(1),  p123-128, Jul 2009.


19.

Efficient differentiation of insulin-producing cells from skin-derived stem cells. Guo,W.,Miao,C.,Liu,S.,Qiu,Z.,Li,J., and Duan, E. Cell Proliferation, Vol.42(1), p49-62, 2009.


20.

Enrichment of Putative Pancreatic Progenitor Cells From Mice by Sorting for Prominin1(CD133)and PDGFRb. Yuichi Hori,Miki Fukomoto,Yoshikazu Kuroda. Stem Cells;0:2008-0192v1,2008


21.

Possibility of insulin-producing cells derived from mouse embryonic stem cells for diabetes treatment. T, Ibii., H, Shimada., S, Miura., E, Fukuma., H, Sato., H, Iwata. Journal of Bioscience and Bioengineering,Vol.103(2), p140-146, Feb 2007.


22.

The dual function of hepatic SOCS3 in insulin resistance in vivo. Torisu, T., Sato, N., Yoshiga, D., Kobayashi, T., Yoshioka, T., Mori, H., Iida, M. and Yoshimura, A. Genes to Cells, 12, p143-154, 2007.


23.

Prolonged remission of diabetes by regeneration of bold italic beta cells in diabetic mice treated with recombinant adenoviral vector expressing glucagon-like peptide-1. Liu, M.J., Shin, S., Li, N., Shigehara, T., Lee, Y.S., Yoon, J.W., and Jun H.S. Molecular Therapy 15: p86-93, 2007.


24.

Possibility of insulin-producing cells derived from mouse embryonic stem cells for diabetes treatment. Ibii, T., Shimada, H, Miura, S., Fukuma, E.,Sato, H.,and Iwata,H. J Bioscience Bioengineering 103: p140-146, 2007.


25.

A human b-cell line for transplantation therapy to control type 1 diabetes. Narushima, M., Kobayashi, N., Okitsu, T., Tanaka, Y., Li, S.A., Chen, Y., Miki, A., Tanaka, K., Nakaji, S., Takei, K., Gutierrez, A.S., Rivas-Carrillo, J.D., Navarro-Alvarez, N., Jun, H.S., Westerman, K.A., Noguchi, H., Lakey, J.R.T.,, Leboulch, P., Tanaka, N., and Yoon, J.W. Nature Biotechnology, Vol. 23(10), p1274-1282, 2005.


产品列表
产品编号 产品名称 产品规格 产品等级 备注
635-07239 (AKRCP-031)LBIS® Mouse C-peptide ELISA kit (U-type)
LBIS®小鼠 C-肽 ELISA试剂盒(U型) 
96 tests

LBIS® 小鼠胰岛素 ELISA 试剂盒(RTU) LBIS® Mouse Insulin ELISA KIT(RTU)

LBIS® 小鼠胰岛素 ELISA 试剂盒(RTU)
LBIS® Mouse Insulin ELISA KIT(RTU)

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

LBIS® Mouse Insulin ELISA KIT(RTU)LBIS® 小鼠胰岛素 ELISA 试剂盒(RTU)                              LBIS® Mouse Insulin ELISA KIT(RTU)

LBIS® 小鼠胰岛素 ELISA 试剂盒(RTU)

LBIS® 小鼠胰岛素 ELISA 试剂盒(RTU)                              LBIS® Mouse Insulin ELISA KIT(RTU)

  

胰岛素是由胰脏内的胰岛β细胞分泌,分子量约 5800,等电点在 5.4 左右的一种蛋白质激素。

  A6-A11、A7-B7、A20-B-19 之间形成二硫键,在酸性溶液或者不含 Zn 离子的中性水溶液中形成二聚体,在含锌离子的中性溶液中,则形成含2个 Zn 离子的六聚体。

  肝脏、肌肉、脂肪组织是主要的靶组织,分别有以下的作用。

肝脏:促进糖原、蛋白质、脂肪酸合成、促进糖类的摄取和利用、抑制糖异生。

肌肉:糖类、氨基酸、K细胞膜通透性增大、促进糖原、蛋白质的合成、抑制蛋白质分解。

脂肪组织:葡萄糖细胞膜通透性增大、促进脂肪酸的合成。

  胰岛素是细胞内的合成单链胰岛素原通过二硫键结合一起形成的。在酶分解作用下被激活,C肽和胰岛素分离。

◆特点


● 测量范围广(100~12,000 pg/mL)

● 短时间测定(总的反应时间:2小时50分钟)

● 微量样品(标准操作:10 μL)可测

● 使用对环境无害的防腐剂

● 全部试剂均为液体,可直接使用

● 精密的测定精度和高再现性

● 有效期限为12个月

◆构成

组成部分

状态

容量

(A) 抗体固相化 96 孔板

洗净后使用

96 wells(8×12)/1 块

(B)胰岛素标准溶液(小鼠)

①12,000 ②4,800 ③2,000 ④800 

⑤300 ⑥100 (pg/mL)

稀释后使用

各100 μL/1 瓶

(C) 缓冲液

即用

60 mL/1 瓶

(D) 生物素结合抗胰岛素抗体

稀释后使用

12 μL/1 瓶

(E) 过氧化物・抗生物素蛋白结合物

稀释后使用

12 μL/1 瓶

(F) 显色液(TMB)

即用

12 mL/1 瓶

(H) 反应终止液(1M H2SO4)※小心轻放

即用

12 mL/1 瓶

( I ) 浓缩洗净液(10×)

稀释后使用

100 mL/1 瓶

封板膜

3 张

使用说明书

1 份

 

◆样品信息

小鼠的血清•血浆•培养液

10 μL/well(标准操作)

※血浆采血建议使用肝素处理血液

◆测量范围

100~12,000 pg/mL(标准曲线范围)

◆Validation data

 

精度测试(组内变异)

 

样品

A

B

C

1

844

1559

5348

2

831

1584

5419

3

829

1555

5377

4

826

1591

5329

5

833

1599

5299

6

841

1525

5304

mean

834

1569

5346

SD

7.04

27.9

45.9

CV(%)

0.84

1.8

0.86

单位:pg/mL

重复性测试(组间变异)

 

测量日/样品

D

E

F

第0天

442

3510

6919

第1天

441

3494

6878

第2天

441

3500

6836

第3天

435

3533

6827

mean

440

3510

6865

SD

3.45

17.0

42.0

CV(%)

0.78

0.48

0.61

单位:pg/mL n=3

  

加标回收测试

 

样品G

添加量

实测值

回收量

回收率(%)

0.00

322

150

466

144

96.0

300

613

291

97.0

600

917

595

99.2

1200

1558

1266

106

单位:pg/mL n=3



样品H

添加量

实测值

回收量

回收率(%)

0.00

1672

500

2162

490

98.0

1500

3202

1530

102

3000

4573

2901

96.7

4500

6001

4329

96.2

单位:pg/mL n=3

 

稀释直线性测试

 

用稀释缓冲液分4次连续稀释2个血清样品的测量结果,直线回归方程的R2在0.9988~0.9998之间。

相关资料


LBIS® 小鼠胰岛素 ELISA 试剂盒(RTU)                              LBIS® Mouse Insulin ELISA KIT(RTU) LBIS® 小鼠胰岛素 ELISA 试剂盒(RTU)                              LBIS® Mouse Insulin ELISA KIT(RTU) LBIS® 小鼠胰岛素 ELISA 试剂盒(RTU)                              LBIS® Mouse Insulin ELISA KIT(RTU)
说明书

ELISA试剂盒选择指南①②

ELISA试剂盒选择指③④

参考文献

 1.

Deficiency of COX7RP, a mitochondrial supercomplex assembly promoting factor, lowers blood glucose level in mice. Shiba S, Ikeda K, Horie-Inoue K, Nakayama A, Tanaka T, Inoue S. Sci Rep. 2017 Aug 8;7(1):7606.


 2.

Long-term dietary nitrite and nitrate deficiency causes the metabolic syndrome, endothelial dysfunction and cardiovascular death in mice. Kina-Tanada M, Sakanashi M, Tanimoto A, Kaname T, Matsuzaki T, Noguchi K, Uchida T, Nakasone J, Kozuka C, Ishida M, Kubota H, Taira Y, Totsuka Y, Kina SI, Sunakawa H, Omura J, Satoh K, Shimokawa H, Yanagihara N, Maeda S, Ohya Y, Matsushita M, Masuzaki H, Arasaki A, Tsutsui M. Diabetologia. 2017 Jun;60(6):1138-1151. 


 3.

α-Mangostin ameliorates hepatic steatosis and insulin resistance by inhibition C-C chemokine receptor 2. Kim HM, Kim YM, Huh JH, Lee ES, Kwon MH, Lee BR, Ko HJ, Chung CH. PLoS One. 2017 Jun 9;12(6):e0179204


 4.

Long-term dietary nitrite and nitrate deficiency causes the metabolic syndrome, endothelial dysfunction and cardiovascular death in mice. Kina-Tanada M, Sakanashi M, Tanimoto A, Kaname T, Matsuzaki T, Noguchi K, Uchida T, Nakasone J, Kozuka C, Ishida M, Kubota H, Taira Y, Totsuka Y, Kina SI, Sunakawa H, Omura J, Satoh K, Shimokawa H, Yanagihara N, Maeda S, Ohya Y, Matsushita M, Masuzaki H, Arasaki A, Tsutsui M. Diabetologia. 2017 Jun;60(6):1138-1151.


 5.

Anti-diabetic effects of luteolin and luteolin-7-O-glucoside on KK-A(y) mice. Zang Y, Igarashi K, Li Y. Biosci Biotechnol Biochem. 2016 Aug;80(8):1580-6.


 6.

Insulin-Inducible SMILE Inhibits Hepatic Gluconeogenesis. Lee JM, Seo WY, Han HS, Oh KJ, Lee YS, Kim DK, Choi S, Choi BH, Harris RA, Lee CH, Koo SH, Choi HS Diabetes. 2016 Jan;65(1):62-73.


 7.

Metabolomics-based search for therapeutic agents for non-alcoholic steatohepatitis Yoshihiko Terashima, Shin Nishiumi , Akihiro Minami, Yuki Kawano, Namiko Hoshi, Takeshi Azuma, Masaru Yoshida, Archives of Biochemistry and Biophysics, Vol.555–556, p55-65, Aug 2014.

 8.

Indirect Effects of Glucagon-Like Peptide-1 Receptor Agonist Exendin-4 on the Peripheral Circadian Clocks in Mice. Hitoshi Ando,Kentarou Ushijima,Akio Fujimura PLoS One. 2013 Nov 15;8(11):e81119.


 9.

Effects of Two Types of Non-Digestible Carbohydrates on Energy Metabolism in Mice. Akiyama, Takashi; Nakatani, Sachie; Kobata, Kenji; Wada, Masahiro Journal of Chitin and Chitosan Science, Vol.2, Number 3, p223-232(10), Sep 2014.


10.

Cinnamtannin A2, a Tetrameric Procyanidin, Increases GLP-1 and Insulin Secretion in Mice. Yamashita Y, Okabe M, Natsume M, Ashida H. Bioscience, Biotechnology, and Biochemistry , Vol.77(4), 2013.


产品列表
产品编号 产品名称 产品规格 产品等级 备注
633-23919  (AKRIN-011RU)LBIS® Mouse Insulin ELISA Kit(RTU) 
LBIS® 小鼠胰岛素 ELISA试剂盒(RTU)
96 tests