Cleaved PARP (Asp214) (D64E10) XP®️ Rabbit mAb 产品图

Cleaved PARP (Asp214) (D64E10)

XP®️ Rabbit mAb
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  • 询价
  • Cell Signaling Technology已认证
  • 5625
  • USA
  • 2026年08月23日
  • western blot,免疫沉淀(IP),免疫组化(IHC),免疫荧光(IF),流式细胞(Flow Cyt)
  • 兔
  • 人,驴
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名:

      Cleaved PARP (Asp214) (D64E10) XP Rabbit mAb

    • 应用范围:

      western blot,免疫沉淀(IP),免疫组化(IHC),免疫荧光(IF),流式细胞(Flow Cyt)

    • 宿主:

      兔

    • 抗原来源:

      /

    • 保质期:

      详见说明书

    • 级别:

      详见MSDS文件

    • 供应商:

      CST

    • 适应物种:

      人,驴

    • 库存:

      大量

    • 是否单克隆:

      多克隆

    • 保存条件:

      -20°c

    XP Monoclonal Antibody

    Product Pathways - Apoptosis

    Cleaved PARP (Asp214) (D64E10) XP® Rabbit mAb #5625

    Applications Reactivity Sensitivity MW (kDa) Isotype
    W IP IHC-P IF-IC F H Mk Endogenous 89 Rabbit IgG

    Applications Key: W=Western Blotting IP=Immunoprecipitation IHC-P=Immunohistochemistry (Paraffin) IF-IC=Immunofluorescence (Immunocytochemistry) F=Flow Cytometry
    Reactivity Key: H=Human Mk=Monkey
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Protocols

    Specificity / Sensitivity

    Cleaved PARP (Asp214) (D64E10) XP® Rabbit mAb detects endogenous levels of the large fragment (89 kDa) of human PARP1 protein produced by caspase cleavage. The antibody does not recognize full length PARP1 or other PARP isoforms.

    Source / Purification

    Monoclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Asp214 in human PARP.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HeLa cells, untreated or treated with Staurosporine #9953 (1 μM, 3 hr), Jurkat cells, untreated or etoposide-treated (25 μM, overnight), and THP-1 cells, untreated or cycloheximide-treated (CHX, 10 μg/ml, overnight) followed by treatment with TNF-α #8902 (20 ng/ml, 4 hr), using Cleaved PARP (Asp214) (D64E10) XP® Rabbit mAb (upper), or total PARP Antibody #9542 (lower).

    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded human tonsil using Cleaved PARP (Asp214) (D64E10) XP® Rabbit mAb.

    Flow Cytometry

    Flow Cytometry

    Flow cytometric analysis of Jurkat cells, untreated (blue) or etoposide-treated (green), using Cleaved PARP (Asp214) (D64E10) XP® Rabbit mAb.

    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of HeLa cells, untreated (left) or treated with Staurosporine #9953 (right), using Cleaved PARP (Asp214) (D64E10) XP® Rabbit mAb (green). Actin filament were labeled with DY-554 phalloidin. Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye).

    Background

    PARP, a 116 kDa nuclear poly (ADP-ribose) polymerase, appears to be involved in DNA repair in response to environmental stress (1). This protein can be cleaved by many ICE-like caspases in vitro (2,3) and is one of the main cleavage targets of caspase-3 in vivo (4,5). In human PARP, the cleavage occurs between Asp214 and Gly215, which separates the PARP amino-terminal DNA binding domain (24 kDa) from the carboxy-terminal catalytic domain (89 kDa) (2,4). PARP helps cells to maintain their viability; cleavage of PARP facilitates cellular disassembly and serves as a marker of cells undergoing apoptosis (6).

    1. Satoh, M.S. and Lindahl, T. (1992) Nature 356, 356-358.
    2. Lazebnik, Y. A. et al. (1994) Nature 371, 346-347.
    3. Cohen, G.M. (1997) Biochem. J. 326, 1-16.
    4. Nicholson, D. W. et al. (1995) Nature 376, 37-43.
    5. Tewari, M. et al. (1995) Cell 81, 801-809.
    6. Oliver, F.J. et al. (1998) J. Biol. Chem. 273, 33533-33539.

    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
    [1]Combined Arctigenin and Curcumin Treatment Induces Redox and Metabolic Stress, AMPK Phosphorylation, and Apoptotic Signaling in Prostate Cancer Cells
    PMID:42796951Nutrients2026-09-10
    [2]A cyclometalated iridium(III) complex induces paraptotic cell death via mitochondrial dysfunction and ER stress in triple-negative breast cancer cells.
    PMID:41669679Front Pharmacol2026-01-17
    [3]Overexpression of ST8Sia1 inhibits tumor progression by TGF-β1 signaling in rectal adenocarcinoma and promotes the tumoricidal effects of CD8+ T cells by granzyme B and perforin.
    PMID:39656552Ann Med2025-12
    [4]Therapeutic targeting de novo purine biosynthesis driven by β-catenin-dependent PPAT upregulation in hepatoblastoma.
    PMID:40097378Cell Death Dis2025-03-17
    [5]CD146 promotes resistance of NSCLC brain metastases to pemetrexed via the NF-κB signaling pathway.
    PMID:39872044Front Pharmacol2025-01-13
    [6]NIR-II light based combinatorial management of hypertrophic scar by inducing autophagy in fibroblasts.
    PMID:39407227J Nanobiotechnology2024-10-15
    [7]Pentapeptide PYRAE triggers ER stress-mediated apoptosis of breast cancer cells in mice by targeting RHBDF1-BiP interaction.
    PMID:37798352Acta Pharmacol Sin2024-02
    [8]Inhibiting ALK-TOPK signaling pathway promotes cell apoptosis of ALK-positive NSCLC.
    PMID:36167821Cell Death Dis2022-09-27
    [9]Buffalo Milk Whey Activates Necroptosis and Apoptosis in a Xenograft Model of Colorectal Cancer.
    PMID:35955595Int J Mol Sci2022-07-30
    [10]Alamandine alleviates hypertension and renal damage via oxidative-stress attenuation in Dahl rats.
    PMID:35022384Cell Death Discov2022-01-12
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