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EDA Antibody Blocking Peptide(

bs-12347P)-500ug
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  • bs-12347P
  • 2025年10月16日
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    产品编号bs-12347P
    英文名称EDA Antibody Blocking Peptide
    中文名称外胚层发育不良蛋白1封闭多肽
    英文别名Ectodysplasin A, membrane form; Ectodermal dysplasia 1, anhidrotic; Ectodermal dysplasia protein; Ectodermal dysplasia, anhidrotic (hypohydrotic); Ectodysplasin A; ECTODYSPLASIN A1 ISOFORM; ECTODYSPLASIN A2 ISOFORM; ECTODYSPLASIN; Ectodysplasin-A; ED1 A1; ED1 A2; ED1; ED1 GENE; Eda A1; Eda A2; eda; EDA protein; EDA protein homolog; EDA_HUMAN; EDA1; EDA1 GENE; EDA2; HED; ODT1; Oligodontia 1; STHAGX1; Ta; Tabby; Tabby protein; X linked anhidroitic ectodermal dysplasia protein; XHED; XLHED.
    纯化方法HPLC
    研究领域

    Developmental Biology > Lineage specification > Ectoderm

    Signal Transduction > Growth Factors/Hormones > TNF

    Stem Cells > Lineage Markers > Ectoderm

    亚基Homotrimer. The homotrimers may then dimerize and form higher-order oligomers.
    亚细胞定位Cell membrane; Single-pass type II membrane protein.
    Ectodysplasin-A, secreted form: Secreted.
    组织特异性Not abundant; expressed in specific cell types of ectodermal (but not mesodermal) origin of keratinocytes, hair follicles, sweat glands. Also in adult heart, liver, muscle, pancreas, prostate, fetal liver, uterus, small intestine and umbilical chord.
    翻译后修饰N-glycosylated.
    Processing by furin produces a secreted form.
    相似性Belongs to the tumor necrosis factor family.
    Contains 1 collagen-like domain.
    功能Seems to be involved in epithelial-mesenchymal signaling during morphogenesis of ectodermal organs. Isoform 1 binds only to the receptor EDAR, while isoform 3 binds exclusively to the receptor XEDAR.
    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The protein encoded by the EDA gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in the EDA gene are a cause of ectodermal dysplasia, anhidrotic, (this is also known as X-linked hypohidrotic ectodermal dysplasia). Several transcript variants encoding many different isoforms have been found for this gene. AltName: ectodermal dysplasia protein; Ectodysplasin-A; EDA protein homolog; Tabby protein; Ectodysplasin-A, membrane form; secreted form EDA-A5.

     

     

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