GLUT2 polyclonal, anti-human, mouse, rat, monkey, pig
€422.00
In stock
SKU
250672
Catalog Nr.: 250672
Size: 0.1 mg
Isotype: Rabbit Ig
Applications: E, WB, IHC
Datasheet
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Size: 0.1 mg
Isotype: Rabbit Ig
Applications: E, WB, IHC
Datasheet
Request Information
Protein Family: Transporters
Pathway and Disease: Carbohydrate Metabolism, Membrane Transport, Metabolic Disorders
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.
Alternate Names: Solute carrier family 2 facilitated glucose transporter member 2, Glucose transporter type 2 liver, GLUT-2, SLC2A2, GLUT2
Application Notes: E: 1:500-1:1,000; WB: 1:200-1:500; IHC: 1:200-1:500
Accession No.: P11168
Antigen: KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human GLUT2.
Format: Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4 with 0.09% sodium azide. Antibody was purified by Protein-G affinity chromatography.
Storage:
Store at -20°C. Minimize freeze-thaw cycles. Product is guaranteed one year from the date of shipment.
Product Citations:
[1] Kosfeld A. et al. 2015. Department of Human Genetics, OE 6300, Hannover Medical School. Jan
135(1):69-87. PMID: 26572137.
[2] Nakayama T. et al. 2010. Am. J. Physiol. Renal Physiol. 298: F712-F720. PMID: 20071464.
Pathway and Disease: Carbohydrate Metabolism, Membrane Transport, Metabolic Disorders
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.
Alternate Names: Solute carrier family 2 facilitated glucose transporter member 2, Glucose transporter type 2 liver, GLUT-2, SLC2A2, GLUT2
Application Notes: E: 1:500-1:1,000; WB: 1:200-1:500; IHC: 1:200-1:500
Accession No.: P11168
Antigen: KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human GLUT2.
Format: Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4 with 0.09% sodium azide. Antibody was purified by Protein-G affinity chromatography.
Storage:
Store at -20°C. Minimize freeze-thaw cycles. Product is guaranteed one year from the date of shipment.
Product Citations:
[1] Kosfeld A. et al. 2015. Department of Human Genetics, OE 6300, Hannover Medical School. Jan
135(1):69-87. PMID: 26572137.
[2] Nakayama T. et al. 2010. Am. J. Physiol. Renal Physiol. 298: F712-F720. PMID: 20071464.
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