Glut1 rabbit pAb
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Glut1 rabbit pAb
Background :
This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein 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. [provided by RefSeq, Apr 2013]Description :
This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein 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. [provided by RefSeq, Apr 2013],UniProt :
P11166Swiss Prot :
P11166Reactivity :
Human; Mouse; RatImmunogen :
The antiserum was produced against synthesized peptide derived from human GLUT1. AA range:441-490Clonality :
PolyclonalSource :
RabbitApplications :
IF; WB; IHC; ELISAConcentration :
1 mg/mlDilution :
IF: 1:50-200 Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.Molecular Weight :
55kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
55kDFragment :
IgGSubcellular Location :
Cell membrane ; Multi-pass membrane protein . Melanosome . Photoreceptor inner segment . Localizes primarily at the cell surface (PubMed:18245775, PubMed:19449892, PubMed:23219802, PubMed:25982116, PubMed:24847886) . Identified by mass spectrometry in melanosome fractions from stage I to stage IV (PubMed:17081065) . .Other Product Names :
SLC2A1; GLUT1; Solute carrier family 2; facilitated glucose transporter member 1; Glucose transporter type 1, erythrocyte/brain; GLUT-1; HepG2 glucose transporterGene ID (Human) :
6513

