KIRREL3 Antibody Blocking Peptide(bs-11864P)-500ug

KIRREL3 Antibody Blocking Pept

ide(bs-11864P)-500ug
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  • bs-11864P
  • 2025年10月16日
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      500ug

    产品编号bs-11864P
    英文名称KIRREL3 Antibody Blocking Peptide
    中文名称肾病样蛋白3封闭多肽
    英文别名Kin of IRRE like 3 (Drosophila); Kin of IRRE like 3; Kin of irregular chiasm like protein 3 ; KIRRE; KIRREL 3; KIRREL-3; MRD4; NEPH2; Nephrin like 2; PRO19814; PRO4502; yUNQ5923; KIRR3_HUMAN.
    纯化方法HPLC
    研究领域

    Neuroscience > Neurology process > Neurogenesis

    亚基Interacts with the C-terminus of NPHS2/podocin. Interacts with CASK.
    亚细胞定位Cell membrane; Single-pass type I membrane protein
    组织特异性Expressed in fetal and adult brain. Also expressed in kidney, specifically in podocytes of kidney glomeruli.
    翻译后修饰Phosphorylation probably regulates the interaction with NSH2. Phosphorylated at Tyr-605 and Tyr-606 by FYN, leading to GRB2 binding (By similarity).
    N-glycosylated (By similarity).
    相似性Belongs to the immunoglobulin superfamily.
    Contains 5 Ig-like C2-type (immunoglobulin-like) domains.
    功能NEPH2 is a member of the nephrin like protein family, which includes NEPH1 (KIRREL; MIM 607428) and NEPH3 (KIRREL2; MIM 607762). The cytoplasmic domains of these proteins interact with the C terminus of podocin (NPHS2; MIM 604766), and the genes are expressed in kidney podocytes, cells involved in ensuring size and charge selective ultrafiltration (Sellin et al., 2003 [PubMed 12424224]).
    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NEPH2 is a 778 amino acid single-pass type I membrane protein that belongs to the nephrin-like protein family and immunoglobulin superfamily. Expressed in both fetal and adult brain, as well as podocytes of kidney glomeruli, NEPH2 contains five Ig-like C2-type (immunoglobulin-like) domains and is thought to plaly a role in the hematopoetic supportive capacity of stroma cells. NEPH2 undergoes alternative splicing to produce two isoforms and contains a C-terminal cytoplasmic domain which it uses to interact with Podocin, a podocyte protein involved in ultrafiltration. Defects in the gene encoding NEPH2 are associated with mental retardation autosomal dominant type 4 (MRD4).

     

     

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