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SQSTM1 抗体

KO Validated SQSTM1 适用: 人, 小鼠, 大鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6567156
发货至: 中国
  • 抗原 See all SQSTM1 抗体
    SQSTM1 (Sequestosome 1 (SQSTM1))
    适用
    • 172
    • 64
    • 61
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    • 4
    • 4
    • 4
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    人, 小鼠, 大鼠
    宿主
    • 146
    • 24
    • 1
    • 1
    克隆类型
    • 145
    • 27
    多克隆
    标记
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    This SQSTM1 antibody is un-conjugated
    应用范围
    • 122
    • 58
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    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
    特异性
    This antibody ist KO validated.
    纯化方法
    Affinity purification
    质量等级
    KO Validated
    免疫原
    Recombinant fusion protein of human SQSTM1 / p62 (NP_001135770.1).
    亚型
    IgG
    Top Product
    Discover our top product SQSTM1 Primary Antibody
  • 应用备注
    WB 1:500-1:2000 IHC 1:50-1:100 IF 1:50-1:100
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    SQSTM1 (Sequestosome 1 (SQSTM1))
    别名
    SQSTM1 / p62 (SQSTM1 产品)
    别名
    SQSTM1 antibody, sqstm1 antibody, MGC79491 antibody, A170 antibody, OSIL antibody, PDB3 antibody, ZIP3 antibody, p60 antibody, p62 antibody, p62B antibody, OSF-6 antibody, Osi antibody, STAP antibody, ZIP antibody, sb:cb621 antibody, zgc:85784 antibody, sequestosome 1 antibody, sequestosome 1 L homeolog antibody, SQSTM1 antibody, sqstm1 antibody, Sqstm1 antibody, sqstm1.L antibody
    背景
    This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B (NF-kB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in sporadic and familial Paget disease of bone.
    分子量

    Observed_MW: 62kDa

    Calculated_MW: 38kDa/47kDa

    基因ID
    8878
    UniProt
    Q13501
    途径
    NF-kappaB Signaling, Neurotrophin Signaling Pathway, Autophagy
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