This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome. [provided by RefSeq, Oct 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PEX13-20-RE | 20 (40 μL) | 200 μL |  |
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| PEX13-20-OR | 20 (40 μL) | 200 μL |  |
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| PEX13-20-GO | 20 (40 μL) | 200 μL |  |
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| PEX13-20-GR | 20 (40 μL) | 200 μL |  |
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| PEX13-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome. [provided by RefSeq, Oct 2008]
Gene Symbol : PEX13
Gene Name : Peroxisomal biogenesis factor 13
Chromosome : CHR 2: 610,176,76-610,519,89
Locus : 2p15
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