Receptor Accessory Protein 1 蛋白
(Receptor Accessory Protein 1 (REEP1))
This gene encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009].
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6 results
REEP1
宿主: 人
宿主: 大肠杆菌（E. Coli）
Recombinant
ELISA, SDS, WB
custom-made
REEP1
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, SDS, WB
custom-made
REEP1
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, SDS, WB
REEP1
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliases for Receptor Accessory Protein 1 蛋白
receptor accessory protein 1 (REEP1) 蛋白receptor accessory protein 1 (Reep1) 蛋白
C2orf23 蛋白
D6Ertd253e 蛋白
HMN5B 蛋白
RGD1305230 蛋白
SPG31 蛋白
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