GTR2 antibody (AA 220-300)
Quick Overview for GTR2 antibody (AA 220-300) (ABIN7228816)
Target
See all GTR2 (RRAGC) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 220-300
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Purpose
- Rabbit Anti-GTR2 Polyclonal Antibody
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Specificity
- The antibody detects endogenous levels of GTR2 protein
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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Immunogen
- Synthesized peptide derived from part region of human GTR2 protein at AA range: 220-300
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA
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Preservative
- ProClin
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Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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Expiry Date
- 12 months
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- GTR2 (RRAGC) (Ras-Related GTP Binding C (RRAGC))
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Alternative Name
- GTR2
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Background
- Solute carrier family 2, facilitated glucose transporter member 2, Glucose transporter type 2, liver, GLUT-2SLC2A2 (Solute Carrier Family 2 Member 2) is a Protein Coding gene. Diseases associated with SLC2A2 include Fanconi-Bickel Syndrome and Diabetes Mellitus, Noninsulin-Dependent. Among its related pathways are Type II diabetes mellitus and Metabolism. SLC2A2 encodes an integral plasma membrane glycoprotein of the liver, islet beta cells, intestine, and kidney epithelium. The encoded protein mediates facilitated bidirectional glucose transport. Because of its low affinity for glucose, it has been suggested as a glucose sensor. Mutations in SLC2A2 are associated with susceptibility to diseases, including Fanconi-Bickel syndrome and noninsulin-dependent diabetes mellitus (NIDDM). Alternative splicing results in multiple transcript variants of SLC2A2.
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Molecular Weight
- 57kD
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Gene ID
- 6514
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UniProt
- P11168
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Pathways
- Autophagy
Target
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