Caspase-9 (C9) Mouse mAb产品图

Caspase-9 (C9) Mouse mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2026年08月22日
  • W
  • H,M,R,Hm,Mk
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    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Caspase-9 (C9) Mouse mAb

    • 抗原

      recombinant human caspase-9 protein

    • 应用范围

      W

    • 供应商

      CST

    • 适应物种

      H,M,R,Hm,Mk

    • 库存

      大量

    • 级别

      详见MSDS文件

    • 保质期

      详见说明书

    • 是否单克隆

      单克隆

    • 保存条件

      -20°c

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key: W=Western Blotting
    Reactivity Key: H=Human M=Mouse R=Rat Hm=Hamster Mk=Monkey
    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 H M R Hm Mk Endogenous 47 /37/35 (H). 51 /39/37 (R,M). Mouse IgG1
    Protocols
    Specificity / Sensitivity

    Caspase-9 (C9) Antibody detects endogenous levels of the pro form of caspase-9 as well as cleaved fragments.

    Source / Purification

    Monoclonal Antibody is produced by immunizing mice with a recombinant human caspase-9 protein.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from Jurkat cells (human), L929 cells (mouse), and C6 cells (rat), untreated or treated with staurosporine or cytochrome c as indicated, using Caspase 9 (C9) Mouse mAb.

    Background

    Caspase-9 (ICE-LAP6, Mch6) is an important member of the cysteine aspartic acid protease (caspase) family (1,2). Upon apoptotic stimulation, cytochrome c released from mitochondria associates with the 47 kDa procaspase-9/Apaf 1. Apaf-1 mediated activation of caspase-9 involves instrinsic proteolytic processing resulting in cleavage at Asp315 and producing a p35 subunit. Another cleavage occurs at Asp330 producing a p37 subunit that can serve to amplify the apoptotic response (3-6). Cleaved caspase-9 further processes other caspase members, including caspase-3 and caspase-7, to initiate a caspase cascade, which leads to apoptosis (7-10).

    1. Duan, H. et al. (1996) J. Biol. Chem. 271, 16720-16724.
    2. Srinivasula, S. M. et al. (1996) J. Biol. Chem. 271, 27099-27106.
    3. Liu, X. et al. (1996) Cell 86, 147-157.
    4. Li, P. et al. (1997) Cell 91, 479-489.
    5. Zou, H. et al. (1999) J. Biol. Chem. 274, 11549-11556.
    6. Srinivasula, S.M. et al. (1998) Mol Cell 1, 949-57.
    7. Deveraux, Q. L. et al. (1998) EMBO J. 17, 2215-2223.
    8. Slee, E. A. et al. (1999) J. Cell Biol. 144, 281-292.
    9. Sun, X. et al. (1999) J. Biol. Chem. 274, 5053-5060.
    10. MacFarlane, M. et al. (1997) J. Cell Biol. 137, 469-479.
    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
    该产品被引用文献
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    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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