Recombinant Rat Slc2a1 protein(207-271aa), His&Myc-tagged
Cat.No. : | Slc2a1-4110R |
Product Overview : | Recombinant Rat Slc2a1 protein(P11167)(207-271aa), fused with N-terminal His&C-terminal Myc tag, was expressed in E. coli. |
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Source : | E. coli |
Species : | Rat |
Tag : | N-His&C-Myc |
Protein length : | 207-271aa |
Form : | If the delivery form is liquid, the default storage buffer is Tris/PBS-based buffer, 5%-50% glycerol. If the delivery form is lyophilized powder, the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, pH 8.0. |
Molecular Mass : | 15.2 kDa |
AASequence : | CPESPRFLLINRNEENRAKSVLKKL RGTADVTRDLQEMKEEGRQMMREKK VTILELFRSPAYRQP |
Purity : | Greater than 90% as determined by SDS-PAGE. |
Storage : | Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles. |
Reconstitution : | We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20°C/-80°C. |
Gene Name : | Slc2a1 solute carrier family 2 (facilitated glucose transporter), member 1 [ Rattus norvegicus ] |
Official Symbol : | Slc2a1 |
Synonyms : | SLC2A1; solute carrier family 2 (facilitated glucose transporter), member 1; solute carrier family 2, facilitated glucose transporter member 1; GLUT-1; solute carrier family 2, member 1; glucose transporter type 1, erythrocyte/brain; Solute carrier family 2 a 1 (facilitated glucose transporter) brain; GTG1; Gtg3; GLUTB; Glut1; RATGTG1; |
Gene ID : | 24778 |
mRNA Refseq : | NM_138827 |
Protein Refseq : | NP_620182 |
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Not For Human Consumption!
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Customer Reviews (3)
Write a reviewQuality product, great results.
Fast and efficient service.
Excellent for immunofluorescence.
Q&As (7)
Ask a questionSLC2A1 facilitates the passive transport of glucose across cell membranes, especially in conditions of low glucose concentration.
Besides glucose, SLC2A1 can also transport other hexoses such as galactose.
SLC2A1 expression is upregulated in response to low glucose availability to ensure sufficient glucose uptake.
Therapeutic interventions could involve managing glucose levels and ketogenic diets to bypass the glucose transport defect in conditions like GLUT1 deficiency syndrome.
It is ubiquitously expressed but is particularly prevalent in erythrocytes and the endothelial cells of the blood-brain barrier.
Mutations or dysregulations in SLC2A1 can lead to glucose transport deficiencies, affecting energy supply to cells.
Mutations in SLC2A1 are associated with GLUT1 deficiency syndrome, which can result in epilepsy, developmental delay, and movement disorders.
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