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RAB3GAP2 Antibody Blocking Pep

tide(bs-11939P)-500ug
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  • bs-11939P
  • 2025年10月16日
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    产品编号bs-11939P
    英文名称RAB3GAP2 Antibody Blocking Peptide
    中文名称RAB3-GTP酶激活蛋白催化亚单位2封闭多肽
    英文别名DKFZp434D245; FLJ14579; KIAA0839; p150; Rab3 GAP p150; Rab3 GAP regulatory subunit; Rab3 GAP150; Rab3 GTPase activating protein 150 kDa subunit; Rab3 GTPase activating protein non catalytic subunit; RAB3 GTPase activating protein subunit 2 (non catalytic); RAB3 GTPase activating protein subunit 2; RAB3GAP150; RGAP iso; RP11 568G11.1; RBGPR_HUMAN.
    纯化方法HPLC
    研究领域

    Developmental Biology > Organogenesis > Nervous system development

    Neuroscience > Neurology process > Neurogenesis

    Neuroscience > Neurotransmission > Secretory Vesicles > Rabs

    Signal Transduction > Protein Trafficking > Vesicle Transport > Regulation

    Signal Transduction > Signaling Pathway > G Protein Signaling > Small G Proteins > Regulators

    亚基The Rab3 GTPase-activating complex is a heterodimer composed of RAB3GAP and RAB3-GAP150. The Rab3 GTPase-activating complex interacts with DMXL2
    亚细胞定位Cytoplasm. Note=In neurons, it is enriched in the synaptic soluble fraction.
    组织特异性Ubiquitous.
    相似性Belongs to the Rab3-GAP regulatory subunit family.
    功能RAB3GAP2 is a regulatory subunit of a GTPase activating protein that has specificity for Rab3 subfamily (RAB3A, RAB3B, RAB3C and RAB3D). Rab3 proteins are involved in regulated exocytosis of neurotransmitters and hormones. Rab3 GTPase-activating complex specifically converts active Rab3-GTP to the inactive form Rab3-GDP. It is required for normal eye and brain development and may participate in neurodevelopmental processes such as proliferation, migration and differentiation before synapse formation, and non-synaptic vesicular release of neurotransmitters.
    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ab 3 GAP p150 is a ubiquitously expressed protein that contains 1,393 amino acids and belongs to the Rab3-GAP regulatory subunit family. Defects in Rab 3 GAP p150 are the cause of Martsolf and Warburg Micro syndrome. Both syndromes are characterized by congenital cataracts, microphthalmia, postnatal microcephaly and developmental delay, and are inherited in an autosomal recessive manner. The Rab3 GTPase-activating complex is a heterodimer composed of RAB3GAP and Rab 3 GAP p150 that interacts with DMXL2. Existing as two alternatively spliced isoforms, the Rab 3 GAP p150 gene is conserved in chimpanzee, dog, cow, rat, chicken, zebrafish, fruit fly, mosquito, A.thaliana and rice. The Rab 3 GAP p150 gene contains 36 exons and maps to human chromosome 1q41.

     

     

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