GLUT2 Peptide
€133.00
In stock
SKU
300121
Protein Family: Transporters
Pathway and Disease: Carbohydrate Metabolism, Membrane Transport, Metabolic Disorders
Alternate Names: Solute carrier family 2 facilitated glucose transporter member 2; Glucose transporter type 2 liver; GLUT-2; SLC2A2; GLUT2
Accession No.: P11168
Description:
Glucose transporter type 2 (GLUT2 or SLC2A2) is a facilitative glucose transporter. This isoform likely mediates the bidirectional transfer of glucose across the plasma membrane of hepatocytes and is responsible for uptake of glucose by the beta cells. GLUT2 is also part of the glucose-sensing mechanism of the beta cell and participate with the Na+/glucose cotransporter in the transcellular transport of glucose in the small intestine and kidney. Defects in GLUT2 are the cause of Fanconi-Bickel syndrome, characterized by hepatorenal glycogen accumulation, proximal renal tubular dysfunction, and impaired utilization of glucose and galactose.
Format:
Each vial contains 0.1 ml peptide in deionized water for a final concentration of 1 mg/ml. Use at 5.6 ug/ml for a 100X excess over antibody for maximum blocking effect.
Sequence:
The synthetic peptide used to raise the antibody Cat. No. 250672 is selected from a sequence within the C-term region of human GLUT2. For blocking experiments, a 10 to 100 fold molar excess to antibody is recommended.
Purity:
> 80% by HPLC
Solubility:
Distilled water for a solution up to 2 mg/ml, otherwise we recommend using acetonitrile.
Storage:
Store at -20°C. The product is hygroscopic and must be protected from light. Product is guaranteed one year from the date of shipment. Following reconstitution, store at -20°C.
Pathway and Disease: Carbohydrate Metabolism, Membrane Transport, Metabolic Disorders
Alternate Names: Solute carrier family 2 facilitated glucose transporter member 2; Glucose transporter type 2 liver; GLUT-2; SLC2A2; GLUT2
Accession No.: P11168
Description:
Glucose transporter type 2 (GLUT2 or SLC2A2) is a facilitative glucose transporter. This isoform likely mediates the bidirectional transfer of glucose across the plasma membrane of hepatocytes and is responsible for uptake of glucose by the beta cells. GLUT2 is also part of the glucose-sensing mechanism of the beta cell and participate with the Na+/glucose cotransporter in the transcellular transport of glucose in the small intestine and kidney. Defects in GLUT2 are the cause of Fanconi-Bickel syndrome, characterized by hepatorenal glycogen accumulation, proximal renal tubular dysfunction, and impaired utilization of glucose and galactose.
Format:
Each vial contains 0.1 ml peptide in deionized water for a final concentration of 1 mg/ml. Use at 5.6 ug/ml for a 100X excess over antibody for maximum blocking effect.
Sequence:
The synthetic peptide used to raise the antibody Cat. No. 250672 is selected from a sequence within the C-term region of human GLUT2. For blocking experiments, a 10 to 100 fold molar excess to antibody is recommended.
Purity:
> 80% by HPLC
Solubility:
Distilled water for a solution up to 2 mg/ml, otherwise we recommend using acetonitrile.
Storage:
Store at -20°C. The product is hygroscopic and must be protected from light. Product is guaranteed one year from the date of shipment. Following reconstitution, store at -20°C.
| Is Featured? | No |
|---|
Write Your Own Review