REEP1 Antibody Blocking Peptide(bs-11752P)-500ug

REEP1 Antibody Blocking Peptid

e(bs-11752P)-500ug
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  • bs-11752P
  • 2025年10月16日
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      500ug

    产品编号bs-11752P
    英文名称REEP1 Antibody Blocking Peptide
    中文名称受体辅助蛋白1封闭多肽
    英文别名C2orf23; Chromosome 2 open reading frame 23; FLJ13110; Receptor accessory protein 1; Receptor expression-enhancing protein 1; Reep1; REEP1_HUMAN; SPG31.
    纯化方法HPLC
    研究领域

    Neuroscience > Neurology process > Neurodegenerative disease

    Neuroscience > Sensory System > Olfactory system

    亚基 Interacts with SPAST and ATL1; it preferentiallyinteracts with SPAST isoform 1. Interacts (via C-terminus) withmicrotubules. Interacts with odorant receptor proteins
    亚细胞定位Membrane. Mitochondrion membrane; Multi-passmembrane protein. Endoplasmic reticulum.
    翻译后修饰Belongs to the DP1 family.
    相似性Belongs to the DP1 family.
    功能May enhance the cell surface expression of odorant receptors.
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料Transport of G protein-coupled receptors (GPCRs) to the cell surface membrane is critical for receptor-ligand recognition. Mammalian GPCR odorant receptors (ORs), when heterologously expressed in cells, are poorly expressed on the cell surface. REEP1 (receptor expression-enhancing protein 1), is a 201 amino acid multi-pass mitochondrion membrane protein that belongs to the DP1 family. REEP1 interacts with odorant receptor proteins and may enhance the cell surface expression of odorant receptors. Mutations in the REEP1 gene are the third most common cause of hereditary spastic paraplegia (HSP) after spastin and atlastin gene mutations. Mutations in the REEP1 gene also cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. The REEP1 gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken, zebrafish, A.thaliana and rice, and maps to human chromosome 2p11.2.

     

     

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