产品名称
Anti-Glucose Transporter-2 Rabbit pAb, liquid, Calbiochem®
biological source
rabbit
antibody form
affinity isolated antibody
antibody product type
primary antibodies
clone
polyclonal
form
liquid
does not contain
preservative
species reactivity
rat, human, mouse
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze
avoid repeated freeze/thaw cycles
dilution
(ELISA (0.5-1 µg/mL)
Immunoblotting (1-10 µg/mL))
isotype
IgG
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
Quality Level
Gene Information
human ... SLC2A2(6514)
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Physical form
In PBS, 0.1% BSA.
Preparation Note
Following initial thaw, aliquot and freeze (-20°C).
Other Notes
Does not recognize other Glut isoforms. Variables associated with assay conditions will dictate the optimal working dilution.
Asano, T., et al. 1989. Nucleic Acids Res. 17, 6386.
Suzue, K., et al. 1989. Nucleic Acids Res. 17, 10099.
Thorens, B., et al. 1988. Cell55, 281.
Suzue, K., et al. 1989. Nucleic Acids Res. 17, 10099.
Thorens, B., et al. 1988. Cell55, 281.
Application
ELISA (0.5-1 µg/ml)
Immunoblotting (1-10 µg/ml)
Immunoblotting (1-10 µg/ml)
Disclaimer
Toxicity: Standard Handling (A)
General description
Anti-Glucose Transporter-2, rabbit polyclonal, recognizes the ~53-61 kDa GLUT-2 protein. It is validated for use in ELISA and Western blotting.
Immunoaffinity purified rabbit polyclonal antibody. Recognizes the ~53-61 kDa Glut-2 protein.
Recognizes the ~53-61 kDa GLUT-2 protein.
Immunogen
Rat
a synthetic peptide corresponding to amino acids in the cytoplasmic domain of rat GLUT-2, conjugated to KLH
Packaging
Please refer to vial label for lot-specific concentration.
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存储类别
12 - Non Combustible Liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Shilpa R Nagarajan et al.
American journal of physiology. Endocrinology and metabolism, 316(4), E578-E589 (2019-01-30)
The liver is a critical tissue for maintaining glucose, fatty acid, and cholesterol homeostasis. Primary hepatocytes represent the gold standard for studying the mechanisms controlling hepatic glucose, lipid, and cholesterol metabolism in vitro. However, access to primary hepatocytes can be
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