cleaved parp1 Search Results


cleaved parp1 p25 rabbit mab  (Genecopoeia)
95
Genecopoeia cleaved parp1 p25 rabbit mab
Cleaved Parp1 P25 Rabbit Mab, supplied by Genecopoeia, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cleaved+parp1/Cleaved+PARP1+p25+Rabbit+mAb/custom%40mab-00533%4033260422
Average 95 stars, based on 1 article reviews
cleaved parp1 p25 rabbit mab - by Bioz Stars, 2026-09
95/100 stars
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cleaved parp1 antibody  (NSJ Bioreagents)
96
NSJ Bioreagents cleaved parp1 antibody
Cleaved Parp1 Antibody, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cleaved+parp1/Cleaved+PARP1+Antibody/custom%40rq5288%4010%2E1353%2Fpsc%2E2004%2E0019
Average 96 stars, based on 1 article reviews
cleaved parp1 antibody - by Bioz Stars, 2026-09
96/100 stars
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cleaved parp 1  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology cleaved parp 1
Cleaved Parp 1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cleaved+parp1/cleaved+PARP-1+Antibody/pmc12389976-86-82-85
Average 96 stars, based on 1 article reviews
cleaved parp 1 - by Bioz Stars, 2026-09
96/100 stars
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cleaved poly  (Elabscience Biotechnology)
96
Elabscience Biotechnology cleaved poly
Cleaved Poly, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cleaved+parp1/Cleaved-PARP1+(G215)+Polyclonal+Antibody/pmc10666272-59-8-33
Average 96 stars, based on 1 article reviews
cleaved poly - by Bioz Stars, 2026-09
96/100 stars
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parp 1 antibody  (Elabscience Biotechnology)
96
Elabscience Biotechnology parp 1 antibody
Parp 1 Antibody, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cleaved+parp1/Cleaved-PARP1+(D214)+Polyclonal+Antibody/pmc07485694-155-0-4
Average 96 stars, based on 1 article reviews
parp 1 antibody - by Bioz Stars, 2026-09
96/100 stars
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cleaved parp  (Biorbyt)
91
Biorbyt cleaved parp
Figure 1. RSC96 cells were injured by high glucose (HG). RSC96 cells were cultivated in HG condition for 48 h. Cells in normal glucose (NG) were considered as con- trol. (A) Cell viability, (B) apoptosis rate, (C,D) cleavage <t>of</t> <t>caspase-3</t> and <t>PARP,</t> (E) ROS generation, and (F,G) expression of neurotrophic proteins were examined by CCK-8 assay, flow cytometry, Western blot and DCFH-DA probe. Data were presented as mean ± SD (n ¼ 3). p < .05 (Student’s t-test).
Cleaved Parp, supplied by Biorbyt, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cleaved+parp1/Cleaved+PARP1+antibody/pm31581849-64-16-53
Average 91 stars, based on 1 article reviews
cleaved parp - by Bioz Stars, 2026-09
91/100 stars
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anti parp1 antibody  (St Johns Laboratory)
90
St Johns Laboratory anti parp1 antibody
Figure 1. RSC96 cells were injured by high glucose (HG). RSC96 cells were cultivated in HG condition for 48 h. Cells in normal glucose (NG) were considered as con- trol. (A) Cell viability, (B) apoptosis rate, (C,D) cleavage <t>of</t> <t>caspase-3</t> and <t>PARP,</t> (E) ROS generation, and (F,G) expression of neurotrophic proteins were examined by CCK-8 assay, flow cytometry, Western blot and DCFH-DA probe. Data were presented as mean ± SD (n ¼ 3). p < .05 (Student’s t-test).
Anti Parp1 Antibody, supplied by St Johns Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cleaved+parp1/Anti-Cleaved-PARP-1+(D214)+antibody/pm35705808-488-0-4
Average 90 stars, based on 1 article reviews
anti parp1 antibody - by Bioz Stars, 2026-09
90/100 stars
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anti-116 kda poly(adp-ribose) polymerase (parp) (1:1000 dilution) mouse monoclonal antibody that also detects the p85 cleavage fragment  (Becton Dickinson)
90
Becton Dickinson anti-116 kda poly(adp-ribose) polymerase (parp) (1:1000 dilution) mouse monoclonal antibody that also detects the p85 cleavage fragment
Figure 1. RSC96 cells were injured by high glucose (HG). RSC96 cells were cultivated in HG condition for 48 h. Cells in normal glucose (NG) were considered as con- trol. (A) Cell viability, (B) apoptosis rate, (C,D) cleavage <t>of</t> <t>caspase-3</t> and <t>PARP,</t> (E) ROS generation, and (F,G) expression of neurotrophic proteins were examined by CCK-8 assay, flow cytometry, Western blot and DCFH-DA probe. Data were presented as mean ± SD (n ¼ 3). p < .05 (Student’s t-test).
Anti 116 Kda Poly(adp Ribose) Polymerase (Parp) (1:1000 Dilution) Mouse Monoclonal Antibody That Also Detects The P85 Cleavage Fragment, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cleaved+parp1/cleaved+parp1++d214++antibody/pmc08656492-99-28-31
Average 90 stars, based on 1 article reviews
anti-116 kda poly(adp-ribose) polymerase (parp) (1:1000 dilution) mouse monoclonal antibody that also detects the p85 cleavage fragment - by Bioz Stars, 2026-09
90/100 stars
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parp-1-dbd cdna  (Promega)
90
Promega parp-1-dbd cdna
Figure 1. RSC96 cells were injured by high glucose (HG). RSC96 cells were cultivated in HG condition for 48 h. Cells in normal glucose (NG) were considered as con- trol. (A) Cell viability, (B) apoptosis rate, (C,D) cleavage <t>of</t> <t>caspase-3</t> and <t>PARP,</t> (E) ROS generation, and (F,G) expression of neurotrophic proteins were examined by CCK-8 assay, flow cytometry, Western blot and DCFH-DA probe. Data were presented as mean ± SD (n ¼ 3). p < .05 (Student’s t-test).
Parp 1 Dbd Cdna, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cleaved+parp1/antibodies+recognizing+solely+caspase+3+cleaved+parp+1++214+215/pmc03945083-77-43-30
Average 90 stars, based on 1 article reviews
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cleaved parp-1 (rabbit polyclonal, 1:2000)  (Bioworld Antibodies)
90
Bioworld Antibodies cleaved parp-1 (rabbit polyclonal, 1:2000)
Levels of protein expression of (A) Bcl-2, (B) Cleaved Caspase 3 and (C) Cleaved <t>PARP-1</t> in the hippocampus of the control, CORT-treated (CORT), M30-treated (M30), CORT and M30 co-treated (CORT+M30) or vehicle groups are summarized. β-actin was an internal control. Data from each group were expressed as mean ± SEM (n = 8). Statistical comparisons between groups were performed using the One way Anova followed by Tukey post hoc test to detect differences in all groups. For Bcl-2, *p < 0.01 when compared with Control, # p < 0.01 when compared with M30, $ p < 0.01 when compared with CORT + M30 groups, ! p < 0.01 when compared with Vehicle. For cleaved caspase 3 and cleaved PARP-1, *p < 0.001 when compared with Control, # p < 0.001 when compared with M30, $ p < 0.001 when compared with CORT + M30 groups, ! p < 0.001 when compared with Vehicle.
Cleaved Parp 1 (Rabbit Polyclonal, 1:2000), supplied by Bioworld Antibodies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cleaved+parp1/cleaved+parp+1++rabbit+polyclonal++1+2000++antibody/pmc05117770-46-83-91
Average 90 stars, based on 1 article reviews
cleaved parp-1 (rabbit polyclonal, 1:2000) - by Bioz Stars, 2026-09
90/100 stars
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hy p80448  (MedChemExpress)
93
MedChemExpress hy p80448
Levels of protein expression of (A) Bcl-2, (B) Cleaved Caspase 3 and (C) Cleaved <t>PARP-1</t> in the hippocampus of the control, CORT-treated (CORT), M30-treated (M30), CORT and M30 co-treated (CORT+M30) or vehicle groups are summarized. β-actin was an internal control. Data from each group were expressed as mean ± SEM (n = 8). Statistical comparisons between groups were performed using the One way Anova followed by Tukey post hoc test to detect differences in all groups. For Bcl-2, *p < 0.01 when compared with Control, # p < 0.01 when compared with M30, $ p < 0.01 when compared with CORT + M30 groups, ! p < 0.01 when compared with Vehicle. For cleaved caspase 3 and cleaved PARP-1, *p < 0.001 when compared with Control, # p < 0.001 when compared with M30, $ p < 0.001 when compared with CORT + M30 groups, ! p < 0.001 when compared with Vehicle.
Hy P80448, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cleaved+parp1/Cleaved-PARP1+Antibody/pm40736991-353-5-6
Average 93 stars, based on 1 article reviews
hy p80448 - by Bioz Stars, 2026-09
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rabbit anti- cleaved-parp1 polyclonal antibody  (Cusabio)
N/A
Rabbit anti-Human Cleaved-PARP1 Polyclonal Antibody
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Image Search Results


Figure 1. RSC96 cells were injured by high glucose (HG). RSC96 cells were cultivated in HG condition for 48 h. Cells in normal glucose (NG) were considered as con- trol. (A) Cell viability, (B) apoptosis rate, (C,D) cleavage of caspase-3 and PARP, (E) ROS generation, and (F,G) expression of neurotrophic proteins were examined by CCK-8 assay, flow cytometry, Western blot and DCFH-DA probe. Data were presented as mean ± SD (n ¼ 3). p < .05 (Student’s t-test).

Journal: Artificial cells, nanomedicine, and biotechnology

Article Title: Notoginsenoside R1 alleviates high glucose-evoked damage in RSC96 cells through down-regulation of miR-503.

doi: 10.1080/21691401.2019.1671434

Figure Lengend Snippet: Figure 1. RSC96 cells were injured by high glucose (HG). RSC96 cells were cultivated in HG condition for 48 h. Cells in normal glucose (NG) were considered as con- trol. (A) Cell viability, (B) apoptosis rate, (C,D) cleavage of caspase-3 and PARP, (E) ROS generation, and (F,G) expression of neurotrophic proteins were examined by CCK-8 assay, flow cytometry, Western blot and DCFH-DA probe. Data were presented as mean ± SD (n ¼ 3). p < .05 (Student’s t-test).

Article Snippet: Following primary antibodies against pro-caspase-3 (orb35276; dilution 1:1000), cleaved-caspase-3 (orb106556; dilution 1:1000), pro-PARP (orb88930; dilution 1:1000), cleaved-PARP (orb323122; dilution 1:2000), NGF (orb379540; dilution 1:1000), BDNF (orb519283; dilution 1:500), PI3K (orb395443; dilution 1:1000), p-PI3K (orb338965; dilution 1:500), AKT (orb29949; dilution 1:500), p-AKT (orb344403; dilution 1:1000), b-catenin (orb500798; dilution 1:1000) and b-actin (orb181785; dilution 1:500, Biorbyt, San Francisco, CA) were utilized in immunoblotting.

Techniques: Expressing, CCK-8 Assay, Flow Cytometry, Western Blot

Figure 2. Notoginsenoside R1 (NGR1) pre-conditioning ameliorated high glucose (HG)-evoked injury in RSC96 cells. (A) NGR1 with various dosages ranged from 10 to 100 lM was utilized to treat RSC96 cells. (B) RSC96 cells were pre-treated with NGR1 and then stimulated by HG. Cell viability was examined by CCK-8 kit. 50 lM was applied as optimum dosage for use in following experiments. (C) Apoptosis rate, (D,E) cleavage of caspase-3 and PARP, (F) ROS generation and (G,H) expression of neurotrophic proteins were examined by flow cytometry, Western blot and DCFH-DA probe. Data were presented as mean ± SD (n ¼ 3). p < .05 (ANOVA).

Journal: Artificial cells, nanomedicine, and biotechnology

Article Title: Notoginsenoside R1 alleviates high glucose-evoked damage in RSC96 cells through down-regulation of miR-503.

doi: 10.1080/21691401.2019.1671434

Figure Lengend Snippet: Figure 2. Notoginsenoside R1 (NGR1) pre-conditioning ameliorated high glucose (HG)-evoked injury in RSC96 cells. (A) NGR1 with various dosages ranged from 10 to 100 lM was utilized to treat RSC96 cells. (B) RSC96 cells were pre-treated with NGR1 and then stimulated by HG. Cell viability was examined by CCK-8 kit. 50 lM was applied as optimum dosage for use in following experiments. (C) Apoptosis rate, (D,E) cleavage of caspase-3 and PARP, (F) ROS generation and (G,H) expression of neurotrophic proteins were examined by flow cytometry, Western blot and DCFH-DA probe. Data were presented as mean ± SD (n ¼ 3). p < .05 (ANOVA).

Article Snippet: Following primary antibodies against pro-caspase-3 (orb35276; dilution 1:1000), cleaved-caspase-3 (orb106556; dilution 1:1000), pro-PARP (orb88930; dilution 1:1000), cleaved-PARP (orb323122; dilution 1:2000), NGF (orb379540; dilution 1:1000), BDNF (orb519283; dilution 1:500), PI3K (orb395443; dilution 1:1000), p-PI3K (orb338965; dilution 1:500), AKT (orb29949; dilution 1:500), p-AKT (orb344403; dilution 1:1000), b-catenin (orb500798; dilution 1:1000) and b-actin (orb181785; dilution 1:500, Biorbyt, San Francisco, CA) were utilized in immunoblotting.

Techniques: CCK-8 Assay, Expressing, Flow Cytometry, Western Blot

Figure 4. Notoginsenoside R1 (NGR1) pre-conditioning ameliorated high glucose (HG)-evoked injury in RSC96 cells through miR-503. (A) miR-503 mimic and its respective control (NC mimic) were transfected into RSC96 cells. Transfection efficiency was examined by qRT-PCR. The transfected or non-transfected cells were then treated by NGR1, HG or both. (B) Cell viability, (C) apoptosis rate, (D,E) cleavage of caspase-3 and PARP, (F) ROS generation, and (G,H) expression of neuro- trophic proteins were examined by CCK-8 assay, flow cytometry, Western blot and DCFH-DA probe. Data were presented as mean ± SD (n ¼ 3). p < .05 (ANOVA).

Journal: Artificial cells, nanomedicine, and biotechnology

Article Title: Notoginsenoside R1 alleviates high glucose-evoked damage in RSC96 cells through down-regulation of miR-503.

doi: 10.1080/21691401.2019.1671434

Figure Lengend Snippet: Figure 4. Notoginsenoside R1 (NGR1) pre-conditioning ameliorated high glucose (HG)-evoked injury in RSC96 cells through miR-503. (A) miR-503 mimic and its respective control (NC mimic) were transfected into RSC96 cells. Transfection efficiency was examined by qRT-PCR. The transfected or non-transfected cells were then treated by NGR1, HG or both. (B) Cell viability, (C) apoptosis rate, (D,E) cleavage of caspase-3 and PARP, (F) ROS generation, and (G,H) expression of neuro- trophic proteins were examined by CCK-8 assay, flow cytometry, Western blot and DCFH-DA probe. Data were presented as mean ± SD (n ¼ 3). p < .05 (ANOVA).

Article Snippet: Following primary antibodies against pro-caspase-3 (orb35276; dilution 1:1000), cleaved-caspase-3 (orb106556; dilution 1:1000), pro-PARP (orb88930; dilution 1:1000), cleaved-PARP (orb323122; dilution 1:2000), NGF (orb379540; dilution 1:1000), BDNF (orb519283; dilution 1:500), PI3K (orb395443; dilution 1:1000), p-PI3K (orb338965; dilution 1:500), AKT (orb29949; dilution 1:500), p-AKT (orb344403; dilution 1:1000), b-catenin (orb500798; dilution 1:1000) and b-actin (orb181785; dilution 1:500, Biorbyt, San Francisco, CA) were utilized in immunoblotting.

Techniques: Control, Transfection, Quantitative RT-PCR, Expressing, CCK-8 Assay, Flow Cytometry, Western Blot

Levels of protein expression of (A) Bcl-2, (B) Cleaved Caspase 3 and (C) Cleaved PARP-1 in the hippocampus of the control, CORT-treated (CORT), M30-treated (M30), CORT and M30 co-treated (CORT+M30) or vehicle groups are summarized. β-actin was an internal control. Data from each group were expressed as mean ± SEM (n = 8). Statistical comparisons between groups were performed using the One way Anova followed by Tukey post hoc test to detect differences in all groups. For Bcl-2, *p < 0.01 when compared with Control, # p < 0.01 when compared with M30, $ p < 0.01 when compared with CORT + M30 groups, ! p < 0.01 when compared with Vehicle. For cleaved caspase 3 and cleaved PARP-1, *p < 0.001 when compared with Control, # p < 0.001 when compared with M30, $ p < 0.001 when compared with CORT + M30 groups, ! p < 0.001 when compared with Vehicle.

Journal: PLoS ONE

Article Title: M30 Antagonizes Indoleamine 2,3-Dioxygenase Activation and Neurodegeneration Induced by Corticosterone in the Hippocampus

doi: 10.1371/journal.pone.0166966

Figure Lengend Snippet: Levels of protein expression of (A) Bcl-2, (B) Cleaved Caspase 3 and (C) Cleaved PARP-1 in the hippocampus of the control, CORT-treated (CORT), M30-treated (M30), CORT and M30 co-treated (CORT+M30) or vehicle groups are summarized. β-actin was an internal control. Data from each group were expressed as mean ± SEM (n = 8). Statistical comparisons between groups were performed using the One way Anova followed by Tukey post hoc test to detect differences in all groups. For Bcl-2, *p < 0.01 when compared with Control, # p < 0.01 when compared with M30, $ p < 0.01 when compared with CORT + M30 groups, ! p < 0.01 when compared with Vehicle. For cleaved caspase 3 and cleaved PARP-1, *p < 0.001 when compared with Control, # p < 0.001 when compared with M30, $ p < 0.001 when compared with CORT + M30 groups, ! p < 0.001 when compared with Vehicle.

Article Snippet: Primary antibodies of SOD-2 (rabbit polyclonal, 1:1000), GPx-1 (goat polyclonal, 1:500), NFκB p65 (rabbit polyclonal, 1:250) and p50 (mouse monoclonal, 1:250), IκBα (mouse monoclonal, 1:500), TNF α (goat polyclonal, 1:80), IL-1β (rabbit polyclonal 1:100), IL-6 (goat polyclonal, 1:1000) and COX-2 (goat polyclonal, 1:100) were purchased from Santa Cruz Biotechnology, CA, USA; Synapsin 1 (rabbit polyclonal, 1:500) and Synaptophysin (rabbit polyclonal, 1:2000) were purchased from Novus Biologicals, USA; PSD95 (rabbit polyclonal 1:500), Cleaved Caspase 3 (rabbit polyclonal 1:500) was purchased from Cell Signaling Technology; Cleaved PARP-1 (rabbit polyclonal, 1:2000) was purchased from Bioworld Technology; IDO-1 (rabbit polyclonal, 1:250) was purchased from antibodies-online (ABIN1714836).

Techniques: Expressing