GLB1 | EBP Ab Blocking Peptide(bs-13369P)-500ug产品图

GLB1 | EBP Ab Blocking Peptide

(bs-13369P)-500ug
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  • bs-13369P
  • 2026年10月10日
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    • 规格:

      500ug

    产品编号bs-13369P
    英文名称GLB1 Antibody Blocking Peptide
    中文名称β-半乳糖苷酶1/β-Gal/弹性蛋白受体1封闭多肽
    英文别名Acid beta galactosidase; Acid beta-galactosidase; Beta galactosidase 1; Beta-galactosidase; BGAL_HUMAN; EBP; EBP, included; Elastin receptor 1 (67kD); Elastin receptor 1 67kDa; Elastin receptor 1; Elastin receptor 1, included; Elastin-binding protein, included; ELNR1; Galactosidase beta 1; GLB 1; GLB1; Lactase; MPS4B; S-GAL, included;
    纯化方法HPLC
    亚细胞定位Isoform 1: Lysosome. Isoform 2: Cytoplasm, perinuclear region. Note=Localized to the perinuclear area of the cytoplasm but not to lysosomes._x000D_
    相似性Belongs to the glycosyl hydrolase 35 family.
    功能Cleaves beta-linked terminal galactosyl residues from gangliosides, glycoproteins, and glycosaminoglycans._x000D_
    Isoform 2 has no beta-galactosidase catalytic activity, but plays functional roles in the formation of extracellular elastic fibers (elastogenesis) and in the development of connective tissue. Seems to be identical to the elastin-binding protein (EBP), a major component of the non-integrin cell surface receptor expressed on fibroblasts, smooth muscle cells, chondroblasts, leukocytes, and certain cancer cell types. In elastin producing cells, associates with tropoelastin intracellularly and functions as a recycling molecular chaperone which facilitates the secretions of tropoelastin and its assembly into elastic fibers.
    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This gene encodes a member of the glycosyl hydrolase 35 family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature lysosomal enzyme. This enzyme catalyzes the hydrolysis of a terminal beta-linked galactose residue from ganglioside substrates and other glycoconjugates. Mutations in this gene may result in GM1-gangliosidosis and Morquio B syndrome. [provided by RefSeq, Nov 2015]

     

     

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