Receptor Accessory Protein 1 Proteine
(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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REEP1
Spezies: Human
Wirt: Escherichia coli (E. coli)
Recombinant
ELISA, SDS, WB
custom-made
REEP1
Spezies: Maus
Wirt: 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
Spezies: Human
Wirt: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, SDS, WB
REEP1
Spezies: Human
Wirt: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
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Aliase für Receptor Accessory Protein 1 Proteine
receptor accessory protein 1 (REEP1) Proteinereceptor accessory protein 1 (Reep1) Proteine
C2orf23 Proteine
D6Ertd253e Proteine
HMN5B Proteine
RGD1305230 Proteine
SPG31 Proteine
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