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$100.00
30μl
30μl -$100.00
100μl -$220.00
200μl -$360.00
RIDACOM Ltd. hotline:
Glut1 Polyclonal Antibody
Antigen:
Solute carrier family 2, facilitated glucose transporter member 1
Synonyms: Glucose transporter type 1, erythrocyte/brain; HepG2 glucose transporter; GTR1_HUMAN; A8K9S6; B2R620; D3DPX0; O75535; P11166; Q147X2
Host:Rabbit
Reactivity:Human; Mouse; Rat
Application:Immunofluorescence; Western Blotting; IHC-P; ELISA
Isotype:IgG
Clonality:Polyclonal
Description:
Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB: 1:500-1:2000, IHC-p: 1:100-1:300, ELISA: 1:40000. Not yet tested in other applications.
Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Formulation:Liquid solution
Precautions:
The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.
Alternative:
SLC2A1
GLUT1
Solute carrier family 2
facilitated glucose transporter member 1
Glucose transporter type 1, erythrocyte/brain
GLUT-1
HepG2 glucose transporter
Buffer form:PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Storage conditions: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.
Delivery conditions:Gel pack with blue ice.
Immunogen:Synthesized peptide derived from the C-terminal region of human Glut1. at AA rangle: 410-490
Usage:
SLC2A1 encodes a major glucose transporter in the mammalian blood-brain barrier. Solute carrier family 2 facilitated glucose transporter member 1 is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia.
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