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Merck
CN
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文件

400062

Sigma-Aldrich

Anti-Glucose Transporter-3 Rabbit pAb

liquid, Calbiochem®

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别名:
Anti-Glut-3
UNSPSC代码:
12352203
NACRES:
NA.41

生物来源

rabbit

质量水平

抗体形式

affinity isolated antibody

抗体产品类型

primary antibodies

克隆

polyclonal

形式

liquid

包含

≤0.1% sodium azide as preservative

种属反应性

human

请勿与下列物质发生反应

rat, mouse

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
avoid repeated freeze/thaw cycles

同位素/亚型

IgG

运输

wet ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... SLC2A3(6515)

一般描述

Anti-Glucose Transporter-3, rabbit polyclonal, recognizes the ~45 kDa GLUT-3 protein. It is validated for use in ELISA, WB, IF, IP, and IHC (frozen sections).
Immunoaffinity purified rabbit polyclonal antibody. Recognizes the ~45 kDa Glut-3 protein.
Recognizes the ~45 kDa GLUT-3 protein.

免疫原

a synthetic peptide corresponding to amino acids near the C-terminus of human GLUT-3, conjugated to KLH

应用

ELISA (0.5-1 µg/ml)

Immunoblotting (1-10 µg/ml)

Frozen Sections (2-20 µg/ml)

Immunofluorescence (2-20 µg/ml)

Immunoprecipitation (see comments)

包装

Please refer to vial label for lot-specific concentration.

警告

Toxicity: Standard Handling (A)

其他说明

Does not cross-react with other Glut isoforms. This antibody has also been reported to work for immunoprecipitation. Variables associated with assay conditions will dictate the optimal working dilution.
Mueckler, M. 1994. Eur. J. Biochem. 219, 713.
Brant, A.M., et al. 1992. Biochem. Soc. Trans. 20, 236S.
Nagamatsu, S., et al. 1992. J. Biol. Chem. 267, 467.
Gould, G.W., et al. 1992. Diabetologia 35, 304.
Kayano, T., et al. 1988. J. Biol. Chem. 263, 15245.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Mark Masin et al.
Cancer & metabolism, 2, 11-11 (2014-08-07)
Alterations in glucose metabolism and epithelial-mesenchymal transition (EMT) constitute two important characteristics of carcinoma progression toward invasive cancer. Despite an extensive characterization of each of them separately, the links between EMT and glucose metabolism of tumor cells remain elusive. Here

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