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Caspase 3 抗体 (N-Term)

CASP3 适用: 人 WB 宿主: 小鼠 Monoclonal AM1-4 unconjugated
产品编号 ABIN187517
发货至: 中国
  • 抗原 See all Caspase 3 (CASP3) 抗体
    Caspase 3 (CASP3)
    抗原表位
    • 19
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    N-Term
    适用
    • 212
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    宿主
    • 226
    • 18
    • 4
    • 2
    • 2
    小鼠
    克隆类型
    • 216
    • 35
    单克隆
    标记
    • 152
    • 19
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    This Caspase 3 antibody is un-conjugated
    应用范围
    • 184
    • 106
    • 101
    • 57
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    • 10
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    Western Blotting (WB)
    特异性
    Species Reactivity: Human, others not tested.
    过滤
    0.2 μm filtered
    免疫原
    Hybridoma produced by the fusion of splenocytes from mice immunized with recombinant human Caspase-3 protein and mouse myeloma cells.
    克隆位点
    AM1-4
    亚型
    IgG1
    Top Product
    Discover our top product CASP3 Primary Antibody
  • 应用备注
    Western Blot The optimal dilution for a specific application should be determined by the researcher.
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Mouse monoclonal antibody against human Caspase-3 (cysteine-requiring aspartate protease-3). Available in 100 ul vials at a concentration of 1 mg/ml (100ug) in PBS with 0.08% sodium azide. Purified and 0.2 µm sterile filtered.
    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
  • 抗原
    Caspase 3 (CASP3)
    别名
    Caspase-3 (CASP3 产品)
    背景
    Caspase-3 along with caspase 7 and 6 form a group of effector caspases that are responsible for the cleavage of multiple substrates including the cytyokeratins, PARP, alpha fodrin, NuMA and others. Caspase-7 occurs in three variant forms. Caspase-3-like activities are required for Fas-mediated apoptosis. However, the role of caspase-1 and caspase-3 in mediating Fas-induced cell death is not clear. Although wild-type, caspase-1(-/-), and caspase-3(-/-) hepatocytes were killed at a similar rate when co-cultured with FasL expressing NIH 3T3 cells, caspase-3(-/-) hepatocytes displayed drastically different morphological changes as well as significantly delayed DNA fragmentation observed in hepatocytes. Cleavage of various caspase substrates implicates apoptotic events, including gesolin, fodin, lamin B, and DFF45/ICAD are delayed or absent. The altered cleavage of these key substrates is likely responsible for the aberrant apoptosis observed in both hepatocytes and thymocytes deficient in caspase-3.
    途径
    Apoptosis, Caspase Cascade in Apoptosis, Sensory Perception of Sound, ER-Nucleus Signaling, Positive Regulation of Endopeptidase Activity, Activated T Cell Proliferation
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