Recombinant Human SLC2A1 protein, His&Myc-tagged
Cat.No. : | SLC2A1-3499H |
Product Overview : | Recombinant Human SLC2A1 protein(P11166)(207-271aa), fused to N-terminal His tag and C-terminal Myc tag, was expressed in E. coli. |
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Source : | E. coli |
Species : | Human |
Tag : | His&Myc |
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 |
Protein length : | 207-271aa |
AA Sequence : | CPESPRFLLINRNEENRAKSVLKKL RGTADVTHDLQEMKEESRQMMREKK VTILELFRSPAYRQP |
Purity : | Greater than 85% 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 : | 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. Our default final concentration of glycerol is 50%. |
Gene Name : | SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1 [ Homo sapiens ] |
Official Symbol : | SLC2A1 |
Synonyms : | SLC2A1; solute carrier family 2 (facilitated glucose transporter), member 1; GLUT, GLUT1; solute carrier family 2, facilitated glucose transporter member 1; DYT18; GLUT-1; hepG2 glucose transporter; glucose transporter type 1, erythrocyte/brain; PED; GLUT; DYT17; GLUT1; GLUT1DS; MGC141895; MGC141896; |
Gene ID : | 6513 |
mRNA Refseq : | NM_006516 |
Protein Refseq : | NP_006507 |
MIM : | 138140 |
UniProt ID : | P11166 |
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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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