推荐产品
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
表单
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)
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.
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
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储存分类代码
10 - Combustible liquids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
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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