This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 alpha subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. This gene is located within the Smith-Magenis syndrome region on chromosome 17. An alternatively spliced transcript variant has been described, but its biological validity has not been determined. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ATPAF2-20-RE | 20 (40 μL) | 200 μL |  |
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| ATPAF2-20-OR | 20 (40 μL) | 200 μL |  |
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| ATPAF2-20-GO | 20 (40 μL) | 200 μL |  |
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| ATPAF2-20-GR | 20 (40 μL) | 200 μL |  |
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| ATPAF2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 alpha subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. This gene is located within the Smith-Magenis syndrome region on chromosome 17. An alternatively spliced transcript variant has been described, but its biological validity has not been determined. [provided by RefSeq, Jul 2008]
Gene Symbol : ATPAF2
Gene Name : ATP synthase mitochondrial F1 complex assembly factor 2
Chromosome : CHR 17: 180,391,68-180,150,58
Locus : 17p11.2
Alt. Genes : ZNF263
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