GDAP1 Antibody Blocking Peptide(bs-11725P)-500ug

GDAP1 Antibody Blocking Peptid

e(bs-11725P)-500ug
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  • bs-11725P
  • 2025年10月16日
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      500ug

    产品编号bs-11725P
    英文名称GDAP1 Antibody Blocking Peptide
    中文名称神经节苷脂诱导分化相关蛋白1封闭多肽
    英文别名Ganglioside induced differentiation associated protein 1; Ganglioside-induced differentiation-associated protein 1; GDAP1; GDAP1_HUMAN.
    纯化方法HPLC
    研究领域

    Neuroscience > Neurology process > Neurodegenerative disease

    Neuroscience > Neurology process > Neurogenesis

    亚基Homodimer.
    亚细胞定位Mitochondrion outer membrane; Multi-pass membrane protein. Cytoplasm (By similarity).
    组织特异性Highly expressed in whole brain and spinal cord. Predominant expression in central tissues of the nervous system not only in neurons but also in Schwann cells.
    相似性Belongs to the GST superfamily.
    Contains 1 GST C-terminal domain.
    Contains 1 GST N-terminal domain.
    功能May function in a signal transduction pathway responsible for ganglioside-induced neurite differentiation. May also have a role in protecting myelin membranes against free radical-mediated damage.
    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Glutathione S-transferases (GSTs) function to conjugate reduced glutathione to many exogenous and endogenous hydrophobic electrophiles. Although it shares the carboxy and amino-terminal glutathione S-transferase domains, GDAP1 is characterized as a GST-like protein because it contains an extended GST domain II and a predicted transmembrane domain, two characteristics which are unusual for GST family members. GDAP1 may function in a signal transduction pathway that is responsible for ganglioside-induced neurite differentiation and also may play a role in protecting myelin membranes from free-radical damage. Mutations in the gene encoding GDAP1 is the cause of many forms of Charcot-Marie-Tooth disease, a common inherited disorder of the peripheral nervous system that is characterized by reduced nerve conduction velocities, slow progressive distal muscle atrophy and absent deep tendon reflexes.

     

     

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