rabbit anti histoneh3 antibody Search Results


rabbit anti phospho histoneh3 antibody  (Cell Signaling Technology Inc)
97
Cell Signaling Technology Inc rabbit anti phospho histoneh3 antibody
Rabbit Anti Phospho Histoneh3 Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+histoneh3+antibody/Phospho-Histone+H3+(Ser10)+Antibody/bio_rxiv__2022__08__24__505108-296-17-19
Average 97 stars, based on 1 article reviews
rabbit anti phospho histoneh3 antibody - by Bioz Stars, 2026-10
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rabbit anti histoneh3  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc rabbit anti histoneh3
Rabbit Anti Histoneh3, supplied by Cell Signaling Technology Inc, 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/rabbit+anti+histoneh3+antibody/Histone+H3+XP+Rabbit+mAb/pm39582024-525-43-46
Average 96 stars, based on 1 article reviews
rabbit anti histoneh3 - by Bioz Stars, 2026-10
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rabbit anti histoneh3 antibody  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc rabbit anti histoneh3 antibody
Rabbit Anti Histoneh3 Antibody, supplied by Cell Signaling Technology Inc, 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/rabbit+anti+histoneh3+antibody/Histone+H3+Antibody/pmc05399407-121-26-29
Average 96 stars, based on 1 article reviews
rabbit anti histoneh3 antibody - by Bioz Stars, 2026-10
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rabbit anti phospho histoneh3 ser10  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology rabbit anti phospho histoneh3 ser10
A) C8161, MV3 and SK-MEL-28 cells treated with increasing concentrations of DTIC were analyzed by flow cytometry and viable cell population size determined as a proportion of untreated control cells. B) Protein lysates from DTIC-treated cells were evaluated for Histone H3 phosphorylation at <t>Ser10</t> (proliferation) and PARP cleavage (apoptosis) by Western blotting. Actin was the loading control. C–D) Cell lines treated with DTIC for 72 hours were analyzed at 24-hour time points for viable cell population size (calculated as a proportion of cells at plating; C) and percentage of cell death (D). E) Histone H3 phosphorylation at Ser10 (green; white arrows) examined by confocal microscopy in DTIC-treated cells. Nuclei were counterstained with DAPI (blue). Scale bar=50μm.
Rabbit Anti Phospho Histoneh3 Ser10, 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/rabbit+anti+histoneh3+antibody/Histone+H3/pmc04398626-58-10-7
Average 96 stars, based on 1 article reviews
rabbit anti phospho histoneh3 ser10 - by Bioz Stars, 2026-10
96/100 stars
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mouse anti phospho histoneh3  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc mouse anti phospho histoneh3
A) C8161, MV3 and SK-MEL-28 cells treated with increasing concentrations of DTIC were analyzed by flow cytometry and viable cell population size determined as a proportion of untreated control cells. B) Protein lysates from DTIC-treated cells were evaluated for Histone H3 phosphorylation at <t>Ser10</t> (proliferation) and PARP cleavage (apoptosis) by Western blotting. Actin was the loading control. C–D) Cell lines treated with DTIC for 72 hours were analyzed at 24-hour time points for viable cell population size (calculated as a proportion of cells at plating; C) and percentage of cell death (D). E) Histone H3 phosphorylation at Ser10 (green; white arrows) examined by confocal microscopy in DTIC-treated cells. Nuclei were counterstained with DAPI (blue). Scale bar=50μm.
Mouse Anti Phospho Histoneh3, supplied by Cell Signaling Technology Inc, 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/rabbit+anti+histoneh3+antibody/Phospho-Histone+H3+(Ser10)+Mouse+mAb/pm40280384-242-13-16
Average 96 stars, based on 1 article reviews
mouse anti phospho histoneh3 - by Bioz Stars, 2026-10
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anti acetyl histoneh3 antibody  (ABclonal Biotechnology)
94
ABclonal Biotechnology anti acetyl histoneh3 antibody
A) C8161, MV3 and SK-MEL-28 cells treated with increasing concentrations of DTIC were analyzed by flow cytometry and viable cell population size determined as a proportion of untreated control cells. B) Protein lysates from DTIC-treated cells were evaluated for Histone H3 phosphorylation at <t>Ser10</t> (proliferation) and PARP cleavage (apoptosis) by Western blotting. Actin was the loading control. C–D) Cell lines treated with DTIC for 72 hours were analyzed at 24-hour time points for viable cell population size (calculated as a proportion of cells at plating; C) and percentage of cell death (D). E) Histone H3 phosphorylation at Ser10 (green; white arrows) examined by confocal microscopy in DTIC-treated cells. Nuclei were counterstained with DAPI (blue). Scale bar=50μm.
Anti Acetyl Histoneh3 Antibody, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+histoneh3+antibody/Acetyl-Histone+H3-K9%2FK14%2FK18%2FK23%2FK27+Rabbit+pAb/pm38331933-792-10-13
Average 94 stars, based on 1 article reviews
anti acetyl histoneh3 antibody - by Bioz Stars, 2026-10
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anti histoneh3  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc anti histoneh3
A) C8161, MV3 and SK-MEL-28 cells treated with increasing concentrations of DTIC were analyzed by flow cytometry and viable cell population size determined as a proportion of untreated control cells. B) Protein lysates from DTIC-treated cells were evaluated for Histone H3 phosphorylation at <t>Ser10</t> (proliferation) and PARP cleavage (apoptosis) by Western blotting. Actin was the loading control. C–D) Cell lines treated with DTIC for 72 hours were analyzed at 24-hour time points for viable cell population size (calculated as a proportion of cells at plating; C) and percentage of cell death (D). E) Histone H3 phosphorylation at Ser10 (green; white arrows) examined by confocal microscopy in DTIC-treated cells. Nuclei were counterstained with DAPI (blue). Scale bar=50μm.
Anti Histoneh3, supplied by Cell Signaling Technology Inc, 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/rabbit+anti+histoneh3+antibody/Histone+H3+XP+Rabbit+mAb/pm39147805-209-31-32
Average 96 stars, based on 1 article reviews
anti histoneh3 - by Bioz Stars, 2026-10
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p s10 histoneh3  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc p s10 histoneh3
A) C8161, MV3 and SK-MEL-28 cells treated with increasing concentrations of DTIC were analyzed by flow cytometry and viable cell population size determined as a proportion of untreated control cells. B) Protein lysates from DTIC-treated cells were evaluated for Histone H3 phosphorylation at <t>Ser10</t> (proliferation) and PARP cleavage (apoptosis) by Western blotting. Actin was the loading control. C–D) Cell lines treated with DTIC for 72 hours were analyzed at 24-hour time points for viable cell population size (calculated as a proportion of cells at plating; C) and percentage of cell death (D). E) Histone H3 phosphorylation at Ser10 (green; white arrows) examined by confocal microscopy in DTIC-treated cells. Nuclei were counterstained with DAPI (blue). Scale bar=50μm.
P S10 Histoneh3, supplied by Cell Signaling Technology Inc, 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/rabbit+anti+histoneh3+antibody/Phospho-Histone+H3+(Ser10)+XP+Rabbit+mAb/pm38273024-319-18-23
Average 96 stars, based on 1 article reviews
p s10 histoneh3 - by Bioz Stars, 2026-10
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mouse anti histoneh3 hrp linked antibody  (Cell Signaling Technology Inc)
95
Cell Signaling Technology Inc mouse anti histoneh3 hrp linked antibody
A) C8161, MV3 and SK-MEL-28 cells treated with increasing concentrations of DTIC were analyzed by flow cytometry and viable cell population size determined as a proportion of untreated control cells. B) Protein lysates from DTIC-treated cells were evaluated for Histone H3 phosphorylation at <t>Ser10</t> (proliferation) and PARP cleavage (apoptosis) by Western blotting. Actin was the loading control. C–D) Cell lines treated with DTIC for 72 hours were analyzed at 24-hour time points for viable cell population size (calculated as a proportion of cells at plating; C) and percentage of cell death (D). E) Histone H3 phosphorylation at Ser10 (green; white arrows) examined by confocal microscopy in DTIC-treated cells. Nuclei were counterstained with DAPI (blue). Scale bar=50μm.
Mouse Anti Histoneh3 Hrp Linked Antibody, supplied by Cell Signaling Technology Inc, 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/rabbit+anti+histoneh3+antibody/Histone+H3+XP+Rabbit+mAb/pm35732988-85-20-26
Average 95 stars, based on 1 article reviews
mouse anti histoneh3 hrp linked antibody - by Bioz Stars, 2026-10
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rabbit anti phospho histoneh3  (Cell Signaling Technology Inc)
93
Cell Signaling Technology Inc rabbit anti phospho histoneh3
A) C8161, MV3 and SK-MEL-28 cells treated with increasing concentrations of DTIC were analyzed by flow cytometry and viable cell population size determined as a proportion of untreated control cells. B) Protein lysates from DTIC-treated cells were evaluated for Histone H3 phosphorylation at <t>Ser10</t> (proliferation) and PARP cleavage (apoptosis) by Western blotting. Actin was the loading control. C–D) Cell lines treated with DTIC for 72 hours were analyzed at 24-hour time points for viable cell population size (calculated as a proportion of cells at plating; C) and percentage of cell death (D). E) Histone H3 phosphorylation at Ser10 (green; white arrows) examined by confocal microscopy in DTIC-treated cells. Nuclei were counterstained with DAPI (blue). Scale bar=50μm.
Rabbit Anti Phospho Histoneh3, supplied by Cell Signaling Technology Inc, 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/rabbit+anti+histoneh3+antibody/Phospho-Histone+H3+(Ser10)+XP+Rabbit+mAb/pmc05293220-45-23-26
Average 93 stars, based on 1 article reviews
rabbit anti phospho histoneh3 - by Bioz Stars, 2026-10
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cyclin b1  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc cyclin b1
A) C8161, MV3 and SK-MEL-28 cells treated with increasing concentrations of DTIC were analyzed by flow cytometry and viable cell population size determined as a proportion of untreated control cells. B) Protein lysates from DTIC-treated cells were evaluated for Histone H3 phosphorylation at <t>Ser10</t> (proliferation) and PARP cleavage (apoptosis) by Western blotting. Actin was the loading control. C–D) Cell lines treated with DTIC for 72 hours were analyzed at 24-hour time points for viable cell population size (calculated as a proportion of cells at plating; C) and percentage of cell death (D). E) Histone H3 phosphorylation at Ser10 (green; white arrows) examined by confocal microscopy in DTIC-treated cells. Nuclei were counterstained with DAPI (blue). Scale bar=50μm.
Cyclin B1, supplied by Cell Signaling Technology Inc, 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/rabbit+anti+histoneh3+antibody/Cyclin+B1+Antibody/pmc08538073-204-33-35
Average 96 stars, based on 1 article reviews
cyclin b1 - by Bioz Stars, 2026-10
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monoclonal histoneh3 antibody  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc monoclonal histoneh3 antibody
A) C8161, MV3 and SK-MEL-28 cells treated with increasing concentrations of DTIC were analyzed by flow cytometry and viable cell population size determined as a proportion of untreated control cells. B) Protein lysates from DTIC-treated cells were evaluated for Histone H3 phosphorylation at <t>Ser10</t> (proliferation) and PARP cleavage (apoptosis) by Western blotting. Actin was the loading control. C–D) Cell lines treated with DTIC for 72 hours were analyzed at 24-hour time points for viable cell population size (calculated as a proportion of cells at plating; C) and percentage of cell death (D). E) Histone H3 phosphorylation at Ser10 (green; white arrows) examined by confocal microscopy in DTIC-treated cells. Nuclei were counterstained with DAPI (blue). Scale bar=50μm.
Monoclonal Histoneh3 Antibody, supplied by Cell Signaling Technology Inc, 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/rabbit+anti+histoneh3+antibody/Histone+H3+Rabbit+mAb/10__1074_slash_jbc__m111__227496-115-0-5
Average 96 stars, based on 1 article reviews
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Image Search Results


A) C8161, MV3 and SK-MEL-28 cells treated with increasing concentrations of DTIC were analyzed by flow cytometry and viable cell population size determined as a proportion of untreated control cells. B) Protein lysates from DTIC-treated cells were evaluated for Histone H3 phosphorylation at Ser10 (proliferation) and PARP cleavage (apoptosis) by Western blotting. Actin was the loading control. C–D) Cell lines treated with DTIC for 72 hours were analyzed at 24-hour time points for viable cell population size (calculated as a proportion of cells at plating; C) and percentage of cell death (D). E) Histone H3 phosphorylation at Ser10 (green; white arrows) examined by confocal microscopy in DTIC-treated cells. Nuclei were counterstained with DAPI (blue). Scale bar=50μm.

Journal: Molecular cancer research : MCR

Article Title: Targeting Nodal in Conjunction with Dacarbazine Induces Synergistic Anti-cancer Effects in Metastatic Melanoma

doi: 10.1158/1541-7786.MCR-14-0077

Figure Lengend Snippet: A) C8161, MV3 and SK-MEL-28 cells treated with increasing concentrations of DTIC were analyzed by flow cytometry and viable cell population size determined as a proportion of untreated control cells. B) Protein lysates from DTIC-treated cells were evaluated for Histone H3 phosphorylation at Ser10 (proliferation) and PARP cleavage (apoptosis) by Western blotting. Actin was the loading control. C–D) Cell lines treated with DTIC for 72 hours were analyzed at 24-hour time points for viable cell population size (calculated as a proportion of cells at plating; C) and percentage of cell death (D). E) Histone H3 phosphorylation at Ser10 (green; white arrows) examined by confocal microscopy in DTIC-treated cells. Nuclei were counterstained with DAPI (blue). Scale bar=50μm.

Article Snippet: Antibodies were: mouse anti-actin (Calbiochem); mouse anti-BCL2 (Santa Cruz Biotechnology); rabbit anti-phospho-HistoneH3 (Ser10), rabbit anti-HistoneH3, and rabbit anti-PARP (Cell Signaling Technology); rabbit anti-Nodal – dialyzed to remove preservative contamination prior to cell culture treatments – (Santa Cruz Biotechnology); mouse anti-Nodal (Abcam – immunohistochemistry); donkey anti-rabbit AlexaFluor-488 and anti-mouse AlexaFluor-546 (Life Technologies).

Techniques: Flow Cytometry, Western Blot, Confocal Microscopy

A–B) Cells were exposed to increasing concentrations of anti-Nodal antibodies or rabbit IgG for 72 hours. Viable cell population size (relative to untreated control; A) and percentage of cell death (B) was determined by flow cytometry (*p<0.05). C) Cell lysates were analyzed by Western blotting for Nodal, phospho-Histone H3 (Ser10) (proliferation), cleaved PARP (pro-apoptotic) and BCL2 (anti-apoptotic).

Journal: Molecular cancer research : MCR

Article Title: Targeting Nodal in Conjunction with Dacarbazine Induces Synergistic Anti-cancer Effects in Metastatic Melanoma

doi: 10.1158/1541-7786.MCR-14-0077

Figure Lengend Snippet: A–B) Cells were exposed to increasing concentrations of anti-Nodal antibodies or rabbit IgG for 72 hours. Viable cell population size (relative to untreated control; A) and percentage of cell death (B) was determined by flow cytometry (*p<0.05). C) Cell lysates were analyzed by Western blotting for Nodal, phospho-Histone H3 (Ser10) (proliferation), cleaved PARP (pro-apoptotic) and BCL2 (anti-apoptotic).

Article Snippet: Antibodies were: mouse anti-actin (Calbiochem); mouse anti-BCL2 (Santa Cruz Biotechnology); rabbit anti-phospho-HistoneH3 (Ser10), rabbit anti-HistoneH3, and rabbit anti-PARP (Cell Signaling Technology); rabbit anti-Nodal – dialyzed to remove preservative contamination prior to cell culture treatments – (Santa Cruz Biotechnology); mouse anti-Nodal (Abcam – immunohistochemistry); donkey anti-rabbit AlexaFluor-488 and anti-mouse AlexaFluor-546 (Life Technologies).

Techniques: Flow Cytometry, Western Blot

C8161 cells were either untreated or treated with 5μg/ml DTIC, followed by no treatment, or 3μg/ml anti-Nodal antibodies or rabbit IgG. End point viable cell number graphed as a percentage of untreated cells (A) and percent cell death (B) were evaluated by flow cytometry. Nodal mRNA levels were evaluated using real-time RT-PCR (C). Protein lysates were analyzed by Western blotting for Nodal, Histone H3 phosphorylation at Ser10 (proliferation) and PARP cleavage (apoptosis). Actin was the loading control. *significant difference from untreated cells and from cells treated only with anti-Nodal antibodies (p<0.05). E) Cellular invasion was evaluated in SK-MEL-28 cells pretreated with DTIC, then exposed to rabbit IgG or anti-Nodal or not further treated (No Antibody) using Matrigel invasion chambers. Invading cells were quantified as percentage of No Antibody control. #p<0.05.

Journal: Molecular cancer research : MCR

Article Title: Targeting Nodal in Conjunction with Dacarbazine Induces Synergistic Anti-cancer Effects in Metastatic Melanoma

doi: 10.1158/1541-7786.MCR-14-0077

Figure Lengend Snippet: C8161 cells were either untreated or treated with 5μg/ml DTIC, followed by no treatment, or 3μg/ml anti-Nodal antibodies or rabbit IgG. End point viable cell number graphed as a percentage of untreated cells (A) and percent cell death (B) were evaluated by flow cytometry. Nodal mRNA levels were evaluated using real-time RT-PCR (C). Protein lysates were analyzed by Western blotting for Nodal, Histone H3 phosphorylation at Ser10 (proliferation) and PARP cleavage (apoptosis). Actin was the loading control. *significant difference from untreated cells and from cells treated only with anti-Nodal antibodies (p<0.05). E) Cellular invasion was evaluated in SK-MEL-28 cells pretreated with DTIC, then exposed to rabbit IgG or anti-Nodal or not further treated (No Antibody) using Matrigel invasion chambers. Invading cells were quantified as percentage of No Antibody control. #p<0.05.

Article Snippet: Antibodies were: mouse anti-actin (Calbiochem); mouse anti-BCL2 (Santa Cruz Biotechnology); rabbit anti-phospho-HistoneH3 (Ser10), rabbit anti-HistoneH3, and rabbit anti-PARP (Cell Signaling Technology); rabbit anti-Nodal – dialyzed to remove preservative contamination prior to cell culture treatments – (Santa Cruz Biotechnology); mouse anti-Nodal (Abcam – immunohistochemistry); donkey anti-rabbit AlexaFluor-488 and anti-mouse AlexaFluor-546 (Life Technologies).

Techniques: Flow Cytometry, Quantitative RT-PCR, Western Blot