Date published: 2025-10-15

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pADPr Antibody (10H): sc-56198

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Datasheets
  • pADPr Antibody (10H) is a mouse monoclonal IgG3 pADPr antibody, cited in 68 publications, provided at 100 µg/ml
  • raised against Poly(ADP-ribose) mixed with methylated bovine serum albumin
  • recommended for detection of poly(ADP-ribose) polymer (pADPr) synthesized by a variety of pADPr polymerase (PARP)-related enzymes including PARP-1, -2, -3, tankyrase, vPARP, sPARP and others. by WB, IF and ELISA; may cross-react with bovine serum albumin; non cross-reactive with ADP-ribose, 5′-AMP, or yeast RNA
  • m-IgG3 BP-HRP is the preferred secondary detection reagent for pADPr Antibody (10H) for WB applications. This reagent is now offered in a bundle with pADPr Antibody (10H) (see ordering information below).

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pADPr Antibody (10H) is a mouse monoclonal IgG3 antibody that detects pADPr in non-species reactive applications such as western blotting (WB), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). Anti-pADPr antibody (10H) is available as a non-conjugated monoclonal isotype antibody. Poly(ADP-ribosylation) is a crucial post-translational modification that plays a significant role in cellular responses to DNA damage, helping to protect proliferating cells from apoptosis. The process is primarily mediated by the poly(ADP-ribose) polymerase (PARP) superfamily of enzymes, which utilize NAD+ as a substrate to transfer ADP-ribose units onto target proteins, resulting in the formation of poly(ADP-ribose) chains. These chains can either exist independently or be covalently attached to proteins, thereby modulating their function and promoting cell survival. The dynamic nature of pADPr chains is essential for various cellular processes, including cell-cycle regulation and the maintenance of genomic integrity, making the study of this modification vital for understanding cellular responses to stress and the mechanisms underlying various diseases.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

pADPr Antibody (10H) References:

  1. Overexpression of dominant negative PARP interferes with tumor formation of HeLa cells in nude mice: evidence for increased tumor cell apoptosis in vivo.  |  Hans, MA., et al. 1999. Oncogene. 18: 7010-5. PMID: 10597301
  2. Analysis of ADP-ribose polymer sizes in intact cells.  |  Gagné, JP., et al. 2001. Mol Cell Biochem. 224: 183-5. PMID: 11693195
  3. B-aggressive lymphoma family proteins have unique domains that modulate transcription and exhibit poly(ADP-ribose) polymerase activity.  |  Aguiar, RC., et al. 2005. J Biol Chem. 280: 33756-65. PMID: 16061477
  4. CDK-dependent activation of poly(ADP-ribose) polymerase member 10 (PARP10).  |  Chou, HY., et al. 2006. J Biol Chem. 281: 15201-7. PMID: 16455663
  5. The expanding role of poly(ADP-ribose) metabolism: current challenges and new perspectives.  |  Gagné, JP., et al. 2006. Curr Opin Cell Biol. 18: 145-51. PMID: 16516457
  6. Collaborator of Stat6 (CoaSt6)-associated poly(ADP-ribose) polymerase activity modulates Stat6-dependent gene transcription.  |  Goenka, S., et al. 2007. J Biol Chem. 282: 18732-9. PMID: 17478423
  7. The diverse biological roles of mammalian PARPS, a small but powerful family of poly-ADP-ribose polymerases.  |  Hassa, PO. and Hottiger, MO. 2008. Front Biosci. 13: 3046-82. PMID: 17981777
  8. Poly(ADP-ribose) polymerase 1 promotes tumor cell survival by coactivating hypoxia-inducible factor-1-dependent gene expression.  |  Elser, M., et al. 2008. Mol Cancer Res. 6: 282-90. PMID: 18314489
  9. Poly (ADP-ribose) polymerase activity regulates apoptosis in HeLa cells after alkylating DNA damage.  |  Liu, X., et al. 2008. Cancer Biol Ther. 7: 934-41. PMID: 18376143
  10. Noncovalent pADPr interaction with proteins and competition with RNA for binding to proteins.  |  Ji, Y. 2011. Methods Mol Biol. 780: 83-91. PMID: 21870256
  11. The immunodetection of pADPr in Drosophila tissues: immunostaining of thick sections; immuno-EM.  |  Jarnik, M. 2011. Methods Mol Biol. 780: 401-11. PMID: 21870274
  12. Detecting and Quantifying pADPr In Vivo.  |  Lamade, AM., et al. 2023. Methods Mol Biol. 2609: 23-42. PMID: 36515827

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

pADPr Antibody (10H)

sc-56198
100 µg/ml
$316.00

pADPr Antibody (10H): m-IgG3 BP-HRP Bundle

sc-550377
100 µg Ab; 40 µg BP
$354.00

Is there a carrier-free version of sc-56198? Perhaps custom? Need to label it with a fluorophore for flow cytometry.

Asked by: pkiela
Thank you for your question. For carrier free products please contact special orders by emailing specialorders@scbt.com
Answered by: BlakeJ
Date published: 2023-05-31

Is this antibody suitable for immunoprecipitation studies?

Asked by: Irshad
Thank you for your question. We haven’t tested this antibody for immunoprecipitation (IP) and so that is not a recommended application at this time. However, we are aware of a few product citations which cite this antibody for that application. Please use the product citation search on our website to search for those specific publications. Or please give us a call in the Technical Service Department for support. https://www.scbt.com/scbt/misc/citationSearch.jsp
Answered by: Technical Support
Date published: 2025-04-30

How much sample should be loaded on SDS-PAGE for detecting pADPr using this antibody?

Asked by: MLis344
Thank you for your question. We recommend loading 40-60µg of sample on your WB for this antibody. Please contact Technical Service if you have any further questions.
Answered by: Technical Support
Date published: 2019-01-26

What is the most recommended diluent for this primary antibody? Is it ok to use 5% BSA in the solution? Thank you in advance.

Asked by: Lucius
Thank you for your question. We recommend diluting the primary antibodies in 5% milk with TBS-T. It is OK to use BSA, but we test them using milk as it tends to give cleaner results. Please contact technical support via phone, email or chat if you have any further questions!
Answered by: Tech Service
Date published: 2020-11-24

I am all out of my donkey anti-mouse secondary antibody, what should I use instead?

Asked by: Cweed
We recommend using one our exclusive Mouse IgG Binding Proteins as a secondary detection reagent. A complete list of available binding proteins is available on our website here: https://www.scbt.com/scbt/browse/support-products-mouse-igg-binding-proteins/_/N-ecrety
Answered by: TechService7
Date published: 2016-12-29
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Rated 5 out of 5 by from Works excellentlyWe used 10H to detect the photocrosslinking activity between 10H antibody and poly-ADP-ribosyl(PAR). Such detection requires antibody to be equipped with superb purity and stability. 10H from Santa Cruz Biotech always give us reproducible results with great sensitivity. The ultra performance of 10H has encouraged us to keep using it in our upcoming Photocrossliking-series research!
Date published: 2021-04-23
Rated 4 out of 5 by from It works for western blotting!It detected high molecular size bands, as expected for poly-ADP-ribosylated proteins, in total nuclear protein lysates from HEK 293T cells (1:500 dilution in 5% milk in TBS/0.1% Tween-20 overnight at 4C). Though, I recommend checking antibody specificity with PARP1-specific siRNAs or pharmacological inhibitors.
Date published: 2018-07-30
Rated 5 out of 5 by from 对实验很有帮助!这个产品对我们的实验帮助很大,这个抗体只有SC才有!使用这个产品之后,做出了很理想的结果!对以后发表文章有用。
Date published: 2018-03-12
Rated 3 out of 5 by from pADPr 10H AntibodyTested for Western Blot analysis in cells collected 15 and 30’ minutes after H2O2 addition and a pre-treatment of 30 minutes of Veliparib, with the relative controls. The signal is not very strong but good and well evaluable.
Date published: 2018-01-15
Rated 4 out of 5 by from Specific detection of poly-ADP-riboseI used this antibody in western blot to detect PAR polymer in cells treated with hydrogen peroxide and LPS. The most striking difference between treated and untreated cells was achieved when membranes were blocked with 0.5% gelatin.
Date published: 2017-12-01
Rated 1 out of 5 by from No IF signalAfter getting a sample, I tried this antibody several times with no success. I used it on both Histochoice and 4% PFA fixed fibroblasts, and used it at dilutions of 1:200, 1:100, and 1:50, and even tried a 1hr DAKO antigen retrieval incubation at 95C, after speaking to technical support, all without being able to get any specific signal.
Date published: 2017-11-03
Rated 4 out of 5 by from well-established Ab for PAR detectionthe antibody works well for IF (1:100) and IP (1-1.5ug); however, it does seem somewhat less robust than preparations I have ordered from other suppliers (at the same concentration)
Date published: 2017-06-01
Rated 5 out of 5 by from Worked wellWorked well in IF in human Hela cells, very satisfied with the performance of the antibody.
Date published: 2017-05-28
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pADPr Antibody (10H) is rated 4.1 out of 5 by 16.
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