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PINK1 抗体

PINK1 适用: 人 WB, IF, IHC (p) 宿主: 小鼠 Monoclonal 38CT20-8-5 unconjugated
产品编号 ABIN387803
发货至: 中国
  • 抗原 See all PINK1 抗体
    PINK1 (PTEN Induced Putative Kinase 1 (PINK1))
    适用
    • 91
    • 50
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    宿主
    • 72
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    • 1
    小鼠
    克隆类型
    • 76
    • 32
    单克隆
    标记
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    This PINK1 antibody is un-conjugated
    应用范围
    • 84
    • 53
    • 48
    • 18
    • 16
    • 6
    • 5
    • 4
    • 3
    • 1
    • 1
    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
    Recombinant PINK1 protein was used to produced this monoclonal antibody.
    克隆位点
    38CT20-8-5
    亚型
    IgG1
    Top Product
    Discover our top product PINK1 Primary Antibody
  • 应用备注
    IF: 1:25. WB: 1:1000. IHC-P: 1:25. IHC-P: 1:25
    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.
    注意事项
    Avoid freeze-thaw cycles.
    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.
    有效期
    6 months
  • 抗原
    PINK1 (PTEN Induced Putative Kinase 1 (PINK1))
    别名
    PINK1 (PINK1 产品)
    别名
    BEST:GH23468 antibody, CG4523 antibody, Dmel\\CG4523 antibody, PINK antibody, PINK1 antibody, dPINK1 antibody, dPink1 antibody, pink1 antibody, wu:fc39e12 antibody, zgc:101729 antibody, BRPK antibody, PARK6 antibody, 1190006F07Rik antibody, AU042772 antibody, AW557854 antibody, mFLJ00387 antibody, PTEN-induced putative kinase 1 antibody, PTEN induced putative kinase 1 antibody, Pink1 antibody, PINK1 antibody, pink1 antibody
    背景
    This gene encodes a serine/threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress-induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease.
    分子量
    62769
    基因ID
    65018
    NCBI登录号
    NP_115785
    UniProt
    Q9BXM7
    途径
    Autophagy
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