GRIP2 Antibody Blocking Peptide(bs-20135P)-500ug

GRIP2 Antibody Blocking Peptid

e(bs-20135P)-500ug
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  • ¥880
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  • bs-20135P
  • 2025年10月16日
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      500ug

    产品编号bs-20135P
    英文名称GRIP2 Antibody Blocking Peptide
    中文名称谷氨酸受体相互作用蛋白2封闭多肽
    英文别名Glutamate receptor-interacting protein 2; GRIP-2; GRIP2_HUMAN; GRIP2; KIAA1719.
    纯化方法HPLC
    亚基Interacts with EFNB1, EFNB3, GRIA2, GRIA3, CSPG4 and GRIPAP1. Can form homomultimers and heteromultimers with GRIP1 (By similarity). Interacts with the C-terminal tail of PRLHR.
    亚细胞定位Cytoplasm. Membrane; Peripheral membrane protein.
    相似性Belongs to the GRIP2 family.
    Contains 7 PDZ (DHR) domains.
    功能May play a role as a localized scaffold for the assembly of a multiprotein signaling complex and as mediator of the trafficking of its binding partners at specific subcellular location in neurons.
    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Glutamate receptors mediate most excitatory neurotransmission in the brain and play an important role in neural plasticity, neural development and neuro-degeneration. The glutamate receptor interacting proteins, GRIP1 and GRIP2, are members of the PDZ domain-containing protein family, and they specifically bind to the carboxy-terminus of AMPA receptor subunits, GluR-2 and GluR-3. GRIP1 and GRIP2 are involved in the targeting of GluR-2 and GluR-3 to the synapse. GRIP1 and GRIP2 are widely expressed in brain, with the highest levels in the cerebral cortex, hippocampus and olfactory bulb. They are both enriched in synaptic plasma and postsynaptic density fractions. GRIP1 is expressed in early development before the expression of AMPA receptors, specifically postnatal days 8-10, while GRIP2 expression parallels that of AMPA receptors during later developmental stages. GRIP1 and GRIP2 may mediate the endocytotic rate of GluR-2 and GluR-3 in response to the phosphorylation of the receptors on Ser 880 by PKC, which is implicated in the induction of cerebellar long-term depression (LTD).

     

     

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