The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CYB5ABA-20-REGO | 20 (40 μL) | 200 μL |
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| CYB5ABA-20-REGR | 20 (40 μL) | 200 μL |
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| CYB5ABA-20-ORGR | 20 (40 μL) | 200 μL |
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| CYB5ABA-20-GOGR | 20 (40 μL) | 200 μL |
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| CYB5ABA-20-GRRE | 20 (40 μL) | 200 μL |
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| CYB5ABA-20-GROR | 20 (40 μL) | 200 μL |
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| CYB5ABA-20-GRGO | 20 (40 μL) | 200 μL |
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| CYB5ABA-20-AQOR | 20 (40 μL) | 200 μL |
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The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]
Gene Symbol : CYB5A
Gene Name : Cytochrome b5 type A
Chromosome : CHR 18: 742,920,15-742,532,91
Locus : 18q22.3
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