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GFAP 抗体

GFAP 适用: 人 WB, IF, IHC (p) 宿主: 小鼠 Monoclonal 183CT3-1-5 unconjugated
产品编号 ABIN659067
发货至: 中国
  • 抗原 See all GFAP 抗体
    GFAP (Glial Fibrillary Acidic Protein (GFAP))
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    小鼠
    克隆类型
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    单克隆
    标记
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    This GFAP antibody is un-conjugated
    应用范围
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    Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    纯化方法
    This antibody is purified through a protein G column, followed by dialysis against PBS.
    免疫原
    This GFAP monoclonal antibody is generated from mouse immunized with GFAP recombinant protein.
    克隆位点
    183CT3-1-5
    亚型
    IgG2b kappa
    Top Product
    Discover our top product GFAP Primary Antibody
  • 应用备注
    IF: 1:10~50. WB: 1:4000. WB: 1:100~500. IHC-P-Leica: 1:1000. IHC: 1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified monoclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    4 °C,-20 °C
    储存方法
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    有效期
    6 months
  • Bajpai, Kerosuo, Tseropoulos, Cummings, Wang, Lei, Liu, Liu, Popescu, Bronner, Andreadis: "Reprogramming Postnatal Human Epidermal Keratinocytes Toward Functional Neural Crest Fates." in: Stem cells (Dayton, Ohio), Vol. 35, Issue 5, pp. 1402-1415, (2018) (PubMed).

  • 抗原
    GFAP (Glial Fibrillary Acidic Protein (GFAP))
    别名
    GFAP (GFAP 产品)
    别名
    GFAP antibody, AI836096 antibody, cb345 antibody, etID36982.3 antibody, gfapl antibody, wu:fb34h11 antibody, wu:fk42c12 antibody, xx:af506734 antibody, zgc:110485 antibody, glial fibrillary acidic protein antibody, GFAP antibody, LOC100136168 antibody, gfap antibody, Gfap antibody
    背景
    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.
    分子量
    49880
    基因ID
    2670
    NCBI登录号
    NP_001124491, NP_001229305, NP_002046
    UniProt
    P14136
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