Retinitis pigmentosa (RP) is a disease that leads to blindness by degeneration of cone photoreceptors. Rods produce factors required for cone viability. The protein encoded by this gene is one of those factors and is similar to a truncated form of thioredoxin. This gene has been proposed to have therapeutic value against RP. [provided by RefSeq, Dec 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NXNL1-20-RE | 20 (40 μL) | 200 μL |  |
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| NXNL1-20-OR | 20 (40 μL) | 200 μL |  |
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| NXNL1-20-GO | 20 (40 μL) | 200 μL |  |
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| NXNL1-20-GR | 20 (40 μL) | 200 μL |  |
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| NXNL1-20-AQ | 20 (40 μL) | 200 μL |  |
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Retinitis pigmentosa (RP) is a disease that leads to blindness by degeneration of cone photoreceptors. Rods produce factors required for cone viability. The protein encoded by this gene is one of those factors and is similar to a truncated form of thioredoxin. This gene has been proposed to have therapeutic value against RP. [provided by RefSeq, Dec 2015]
Gene Symbol : NXNL1
Gene Name : Nucleoredoxin like 1
Chromosome : CHR 19: 174,609,15-174,554,24
Locus : 19p13.11
Alt. Genes : RBM12
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