GFAP Rabbit pAb, AP conjugated(bs-0199R-AP)-100ul

GFAP Rabbit pAb, AP conjugated

(bs-0199R-AP)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-0199R-AP
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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      100ul

    产品编号bs-0199R-AP
    英文名称GFAP Rabbit pAb, AP conjugated
    中文名称AP标记的胶质纤维酸性蛋白抗体
    英文别名Astrocyte Marker; FLJ45472; GFAP; Glial Fibrillary Acidic Protein; Intermediate filament protein; GFAP_HUMAN.
    产品应用IHC-P=1:100-500, IHC-F=1:200-1000

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human GFAP
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Neuroscience > Cell Adhesion Proteins > Cytoskeletal Proteins > Intermediate Filaments

    Neuroscience > Cell Type Marker > Glia marker > Astrocyte marker

    Signal Transduction > Cytoskeleton / ECM > Cytoskeleton > Intermediate Filaments > Class II > GFAP

    Stem Cells > Neural Stem Cells > Glial Restricted Lineage > Astrocyte

    Tags & Cell Markers > Cell Type Markers > Neuroscience Markers > Glial

    亚基Interacts with SYNM. Isoform 3 interacts with PSEN1 (via N-terminus).
    亚细胞定位Cytoplasm. Note=Associated with intermediate filaments.
    组织特异性Expressed in cells lacking fibronectin.
    翻译后修饰Phosphorylated by PKN1.
    相似性Belongs to the intermediate filament family.
    功能GFAP, a class-III intermediate filament, is a cell-specific marker that, during the development of the central nervous system, distinguishes astrocytes from other glial cells.
    保存条件Shipped at 4℃. Store at -20°C 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 one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]

     

    应用推荐稀释比例
    {IHC-P}{1:100-500}
    {IHC-F}{1:200-1000}

     

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