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Caspase-8 (1C12) Mouse mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年09月04日
  • W, IP
  • H
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Caspase-8 (1C12) Mouse mAb

    • 抗原

      synthetic peptide corresponding to the carboxy-terminal sequence of the p18 fragment of human caspase-8

    • 应用范围

      W, IP

    • 保质期

      详见说明书

    • 供应商

      CST

    • 库存

      大量

    • 适应物种

      H

    • 级别

      详见MSDS文件

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      200 ul (20 western blots)/600 ul (60 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:200 ul (20 western blots)产品价格:¥请询价
    规格:600 ul (60 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting  IP=Immunoprecipitation
    Reactivity Key:  H=Human
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Isotype
    W IP H Endogenous 18, 43, 57 Mouse IgG1
    Protocols
    Specificity / Sensitivity

    Caspase-8 (1C12) Mouse mAb detects endogenous levels of full length caspase-8 (57 kDa), the cleaved intermediate p43/p41 and the caspase-8 active fragment p18. This antibody does not cross-react with other caspases.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to the carboxy-terminal sequence of the p18 fragment of human caspase-8. Antibody is supplied in HEPES buffer with 50% glycerol and less than 0.02% sodium azide.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from SKW6.4 cells, untreated or anti-Fas-treated (1 µg/ml), and Jurkat cells, untreated or etoposide-treated (25 µM), using Caspase-8 (1C12) Mouse mAb.

    Background

    Apoptosis induced through the CD95 receptor (Fas/APO-1) and tumor necrosis factor receptor 1 (TNFR1) activates caspase-8 and leads to the release of the caspase-8 active fragments, p18 and p10 (1-3). Activated caspase-8 cleaves and activates downstream effector caspases such as caspase-1, -3, -6, and -7. Caspase-3 ultimately elicits the morphological hallmarks of apoptosis, including DNA fragmentation and cell shrinkage.

    1. Muzio, M. et al. (1996) Cell 85, 817-827.
    2. Boldin, M.P. et al. (1996) Cell 85, 803-815.
    3. Fernandes-Alnemri, T. et al. (1996) Proc. Natl. Acad. Sci. USA 93, 7464-7469.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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    图标文献和实验
    相关实验
    • Purification of mAb (IgG)

      (adjust pH to 7.8 with Binding buffer; red color) to the Protein A column.Mouse antibodies of the IgG1 subclass do not have a high affinity for protein A. Purification on protein A beads using standard conditions will yield approximately 1/10

    • Purification of mAb (IgG)

        Purification of mAb (IgG) by Chang-Duk Jun, 03/14/2000 Purpose Materials Antibody 7E3 , 2L sup grown in flasks, frozen and thawed overnight. BioRad Affi-Gel Protein A MAPS II Buffers

    • T-Cell Activation Using mAb to CD3

      One of the most common ways to assess T cell activation is to measure T cell proliferation upon in vitro stimulation of T cells via antigen or agonistic antibodies to TCR. This protocol is written as a starting point for examining in vitro proliferation of mouse

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