The protein encoded by this gene is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC16A1-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC16A1-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC16A1-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC16A1-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC16A1-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2009]
Gene Symbol : SLC16A1
Gene Name : Solute carrier family 16 member 1
Chromosome : CHR 1: 112,956,352-112,911,846
Locus : 1p13.2
Alt. Genes : AKAP9
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