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anti par monoclonal antibody  (R&D Systems)


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    Structured Review

    R&D Systems anti par monoclonal antibody
    Anti Par Monoclonal Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 62 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+par+padpr+monoclonal+antibody/PAR%2FpADPr+Antibody/pmc12363383-52-3-7
    Average 95 stars, based on 62 article reviews
    anti par monoclonal antibody - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Incubation:

    Article Title: A Bifunctional PARP-HDAC Inhibitor with Activity in Ewing Sarcoma
    Article Snippet: .. Following two washes with PBS and one wash with 3% BSA-PBS, cells were incubated for 1 hour at room temperature with anti-PAR/ pADPr monoclonal antibody (R&D Systems, catalog No. 4335-MC100; RRID:AB_2572318) diluted 1:250 in 3% BSA-PBS. .. Plates were washed twice with 3% BSA-PBS, once with PBS, twice with PBS-T, twice with PBS, and once with 3% BSA-PBS and then incubated with goat anti-mouse IgG-FITC (Thermo Scientific, catalog No. F-2761; RRID:AB_2536524) diluted 1:1,000 in 3% BSA-PBS for 1 hour at room temperature.

    Article Title: A bi-functional PARP-HDAC inhibitor with activity in Ewing sarcoma
    Article Snippet: .. Following 2x washes with PBS and 1x wash with 3% BSA-PBS, cells were incubated for 1 hour at RT with anti-PAR/pADPr monoclonal antibody (R&D Systems cat# 4335-MC-100) diluted 1:250 in 3% BSA-PBS. .. Plates were washed 2x with 3% BSA-PBS, 1x with PBS, 2x with PBS-T, 2x with PBS and 1x with 3% BSA-PBS, then incubated with goat anti-mouse IgG-FITC (Thermo Scientific cat# F-2761) diluted 1:1000 in 3% BSA-PBS for 1 hour at RT.

    Article Title: A Bifunctional PARP-HDAC Inhibitor with Activity in Ewing Sarcoma
    Article Snippet: .. Following two washes with PBS and one wash with 3% BSA-PBS, cells were incubated for 1 hour at room temperature with anti-PAR/pADPr monoclonal antibody (R&D Systems, catalog No. 4335-MC-100; RRID:AB_2572318) diluted 1:250 in 3% BSA-PBS. .. Plates were washed twice with 3% BSA-PBS, once with PBS, twice with PBS-T, twice with PBS, and once with 3% BSA-PBS and then incubated with goat anti-mouse IgG-FITC (Thermo Scientific, catalog No. F-2761; RRID:AB_2536524) diluted 1:1,000 in 3% BSA-PBS for 1 hour at room temperature.

    Virus:

    Article Title: PARP1-driven repair of topoisomerase IIIα DNA-protein crosslinks by FEN1.
    Article Snippet: Article PARP1-driven repair of top oisomerase IIIa DNAprotein crosslinks by FEN1

    Recombinant:

    Article Title: PARP1-driven repair of topoisomerase IIIα DNA-protein crosslinks by FEN1.
    Article Snippet: Article PARP1-driven repair of top oisomerase IIIa DNAprotein crosslinks by FEN1

    Modification:

    Article Title: PARP1-driven repair of topoisomerase IIIα DNA-protein crosslinks by FEN1.
    Article Snippet: Article PARP1-driven repair of top oisomerase IIIa DNAprotein crosslinks by FEN1

    Protease Inhibitor:

    Article Title: PARP1-driven repair of topoisomerase IIIα DNA-protein crosslinks by FEN1.
    Article Snippet: Article PARP1-driven repair of top oisomerase IIIa DNAprotein crosslinks by FEN1

    Transfection:

    Article Title: PARP1-driven repair of topoisomerase IIIα DNA-protein crosslinks by FEN1.
    Article Snippet: Article PARP1-driven repair of top oisomerase IIIa DNAprotein crosslinks by FEN1

    Chromatin Immunoprecipitation:

    Article Title: PARP1-driven repair of topoisomerase IIIα DNA-protein crosslinks by FEN1.
    Article Snippet: Article PARP1-driven repair of top oisomerase IIIa DNAprotein crosslinks by FEN1

    Magnetic Beads:

    Article Title: PARP1-driven repair of topoisomerase IIIα DNA-protein crosslinks by FEN1.
    Article Snippet: Article PARP1-driven repair of top oisomerase IIIa DNAprotein crosslinks by FEN1



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    Fig. 5. Western blotting performed in gonad homogenates from unexposed (Unx) and exposed M. galloprovincialis to 1 nM, 10 and 100 nM Cr(VI); (a) 12 % (SDS- PAGE); (b) anti-PARP immunoblotting; (c) <t>anti-PAR</t> immunoblotting; (d) densitometric analysis of 50 kDa bands immunopositive to anti-PARP; (e) densitometric analysis band immunopositive to anti-PARP with molecular weight between 30 and 40 kDa; (f) Kruskal-Wallis test followed by Dunn’s multiple comparison test was used to highlight statistically significant differences between gonad homogenates. The data are showed as mean ± SD and the minimum level of acceptable sig- nificance was set at p < 0.05.
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    Fig. 5. Western blotting performed in gonad homogenates from unexposed (Unx) and exposed M. galloprovincialis to 1 nM, 10 and 100 nM Cr(VI); (a) 12 % (SDS- PAGE); (b) anti-PARP immunoblotting; (c) <t>anti-PAR</t> immunoblotting; (d) densitometric analysis of 50 kDa bands immunopositive to anti-PARP; (e) densitometric analysis band immunopositive to anti-PARP with molecular weight between 30 and 40 kDa; (f) Kruskal-Wallis test followed by Dunn’s multiple comparison test was used to highlight statistically significant differences between gonad homogenates. The data are showed as mean ± SD and the minimum level of acceptable sig- nificance was set at p < 0.05.
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    R&D Systems mouse monoclonal anti par polymermonoclonal antibody
    Fig. 5. Western blotting performed in gonad homogenates from unexposed (Unx) and exposed M. galloprovincialis to 1 nM, 10 and 100 nM Cr(VI); (a) 12 % (SDS- PAGE); (b) anti-PARP immunoblotting; (c) <t>anti-PAR</t> immunoblotting; (d) densitometric analysis of 50 kDa bands immunopositive to anti-PARP; (e) densitometric analysis band immunopositive to anti-PARP with molecular weight between 30 and 40 kDa; (f) Kruskal-Wallis test followed by Dunn’s multiple comparison test was used to highlight statistically significant differences between gonad homogenates. The data are showed as mean ± SD and the minimum level of acceptable sig- nificance was set at p < 0.05.
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    Image Search Results


    Fig. 5. Western blotting performed in gonad homogenates from unexposed (Unx) and exposed M. galloprovincialis to 1 nM, 10 and 100 nM Cr(VI); (a) 12 % (SDS- PAGE); (b) anti-PARP immunoblotting; (c) anti-PAR immunoblotting; (d) densitometric analysis of 50 kDa bands immunopositive to anti-PARP; (e) densitometric analysis band immunopositive to anti-PARP with molecular weight between 30 and 40 kDa; (f) Kruskal-Wallis test followed by Dunn’s multiple comparison test was used to highlight statistically significant differences between gonad homogenates. The data are showed as mean ± SD and the minimum level of acceptable sig- nificance was set at p < 0.05.

    Journal: Chemico-biological interactions

    Article Title: Molecular and toxicological mechanisms behind the effects of chromium (VI) on the male reproductive system of Mytilus galloprovincialis: First evidence for poly-ADP-ribosylation of protamine-like II.

    doi: 10.1016/j.cbi.2024.111186

    Figure Lengend Snippet: Fig. 5. Western blotting performed in gonad homogenates from unexposed (Unx) and exposed M. galloprovincialis to 1 nM, 10 and 100 nM Cr(VI); (a) 12 % (SDS- PAGE); (b) anti-PARP immunoblotting; (c) anti-PAR immunoblotting; (d) densitometric analysis of 50 kDa bands immunopositive to anti-PARP; (e) densitometric analysis band immunopositive to anti-PARP with molecular weight between 30 and 40 kDa; (f) Kruskal-Wallis test followed by Dunn’s multiple comparison test was used to highlight statistically significant differences between gonad homogenates. The data are showed as mean ± SD and the minimum level of acceptable sig- nificance was set at p < 0.05.

    Article Snippet: After repeated washings in Tris-buffered saline (50 mM Tris-HCl and 150 mM NaCl, pH 8.0), the immunoblotting was carried out using monoclonal anti-poly ADP-ribose (PAR) antibody (sc-56198, Santa Cruz, Biotechnology, Inc., Texas, USA, 1:500) and as anti-mouse secondary antibody was utilized horseradish peroxidase (HRP)-conjugated (sc-525409, Santa Cruz Biotechnology, Inc., Texas, USA, 1:2000).

    Techniques: Western Blot, SDS Page, Molecular Weight, Comparison

    Fig. 7. Western blotting carried out on PL proteins and H1 histone of M. galloprovincialis unexposed (Unx) and exposed to 1 nM, 10 and 100 nMCr(VI). (a):11.2 % acetic acid-urea polyacrylamide gel (AU-PAGE). (b): anti-PAR immunoblotting.

    Journal: Chemico-biological interactions

    Article Title: Molecular and toxicological mechanisms behind the effects of chromium (VI) on the male reproductive system of Mytilus galloprovincialis: First evidence for poly-ADP-ribosylation of protamine-like II.

    doi: 10.1016/j.cbi.2024.111186

    Figure Lengend Snippet: Fig. 7. Western blotting carried out on PL proteins and H1 histone of M. galloprovincialis unexposed (Unx) and exposed to 1 nM, 10 and 100 nMCr(VI). (a):11.2 % acetic acid-urea polyacrylamide gel (AU-PAGE). (b): anti-PAR immunoblotting.

    Article Snippet: After repeated washings in Tris-buffered saline (50 mM Tris-HCl and 150 mM NaCl, pH 8.0), the immunoblotting was carried out using monoclonal anti-poly ADP-ribose (PAR) antibody (sc-56198, Santa Cruz, Biotechnology, Inc., Texas, USA, 1:500) and as anti-mouse secondary antibody was utilized horseradish peroxidase (HRP)-conjugated (sc-525409, Santa Cruz Biotechnology, Inc., Texas, USA, 1:2000).

    Techniques: Western Blot