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bax  (OriGene)
94
OriGene bax
Alcohol exposure induces anastasis in esophageal epithelial cells. A . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for <t>BAX</t> and endoG. A Texas Red- or FITC-conjugated secondary antibody was used to develop the signal for BAX (red) and endoG (green). Cell nuclei were counterstained with DAPI. Scale bar = 10 μm. B . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 5 min, 30 min, or 2, 6, and 12 h. Cells were fixed in 4% paraformaldehyde and stained for BAX and endoG. Quantitative analyses showing percentages of BAX-endoG co-localized cells in the total number of cells. C . An equal number of HEEC or Het1A cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. Quantitative analyses showing the ratio of endoG to BAX per cell. * indicates a significant change compared to the control. D . An equal number of HEEC or Het1A cells was seeded in 6-well plates and incubated with the complete medium (control) or the medium containing 5.0% ethanol (EtOH) for 2–12 h. Protein was extracted and analyzed by Western blotting for <t>BAX.</t> <t>GAPDH</t> was used as a loading control. E . Quantitative analyses of BAX expression against GAPDH
Bax, supplied by OriGene, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bax - by Bioz Stars, 2026-09
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mouse anti bax monoclonal antibody  (Wuhan Sanying Biotechnology)
86
Wuhan Sanying Biotechnology mouse anti bax monoclonal antibody
Alcohol exposure induces anastasis in esophageal epithelial cells. A . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for <t>BAX</t> and endoG. A Texas Red- or FITC-conjugated secondary antibody was used to develop the signal for BAX (red) and endoG (green). Cell nuclei were counterstained with DAPI. Scale bar = 10 μm. B . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 5 min, 30 min, or 2, 6, and 12 h. Cells were fixed in 4% paraformaldehyde and stained for BAX and endoG. Quantitative analyses showing percentages of BAX-endoG co-localized cells in the total number of cells. C . An equal number of HEEC or Het1A cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. Quantitative analyses showing the ratio of endoG to BAX per cell. * indicates a significant change compared to the control. D . An equal number of HEEC or Het1A cells was seeded in 6-well plates and incubated with the complete medium (control) or the medium containing 5.0% ethanol (EtOH) for 2–12 h. Protein was extracted and analyzed by Western blotting for <t>BAX.</t> <t>GAPDH</t> was used as a loading control. E . Quantitative analyses of BAX expression against GAPDH
Mouse Anti Bax Monoclonal Antibody, supplied by Wuhan Sanying Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse anti bax monoclonal antibody - by Bioz Stars, 2026-09
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monoclonal mouse antibodies targeting bax  (Biogenex)
86
Biogenex monoclonal mouse antibodies targeting bax
Alcohol exposure induces anastasis in esophageal epithelial cells. A . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for <t>BAX</t> and endoG. A Texas Red- or FITC-conjugated secondary antibody was used to develop the signal for BAX (red) and endoG (green). Cell nuclei were counterstained with DAPI. Scale bar = 10 μm. B . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 5 min, 30 min, or 2, 6, and 12 h. Cells were fixed in 4% paraformaldehyde and stained for BAX and endoG. Quantitative analyses showing percentages of BAX-endoG co-localized cells in the total number of cells. C . An equal number of HEEC or Het1A cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. Quantitative analyses showing the ratio of endoG to BAX per cell. * indicates a significant change compared to the control. D . An equal number of HEEC or Het1A cells was seeded in 6-well plates and incubated with the complete medium (control) or the medium containing 5.0% ethanol (EtOH) for 2–12 h. Protein was extracted and analyzed by Western blotting for <t>BAX.</t> <t>GAPDH</t> was used as a loading control. E . Quantitative analyses of BAX expression against GAPDH
Monoclonal Mouse Antibodies Targeting Bax, supplied by Biogenex, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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monoclonal mouse antibodies targeting bax - by Bioz Stars, 2026-09
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mouse monoclonal anti bax antibody  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology mouse monoclonal anti bax antibody
Alcohol exposure induces anastasis in esophageal epithelial cells. A . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for <t>BAX</t> and endoG. A Texas Red- or FITC-conjugated secondary antibody was used to develop the signal for BAX (red) and endoG (green). Cell nuclei were counterstained with DAPI. Scale bar = 10 μm. B . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 5 min, 30 min, or 2, 6, and 12 h. Cells were fixed in 4% paraformaldehyde and stained for BAX and endoG. Quantitative analyses showing percentages of BAX-endoG co-localized cells in the total number of cells. C . An equal number of HEEC or Het1A cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. Quantitative analyses showing the ratio of endoG to BAX per cell. * indicates a significant change compared to the control. D . An equal number of HEEC or Het1A cells was seeded in 6-well plates and incubated with the complete medium (control) or the medium containing 5.0% ethanol (EtOH) for 2–12 h. Protein was extracted and analyzed by Western blotting for <t>BAX.</t> <t>GAPDH</t> was used as a loading control. E . Quantitative analyses of BAX expression against GAPDH
Mouse Monoclonal Anti Bax Antibody, 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/bax+mouse+monoclonal+antibody/Bax+Antibody/pm41671579-121-132-139
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mouse monoclonal anti bax antibody - by Bioz Stars, 2026-09
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mouse monoclonal anti human bax antibody  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology mouse monoclonal anti human bax antibody
Alcohol exposure induces anastasis in esophageal epithelial cells. A . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for <t>BAX</t> and endoG. A Texas Red- or FITC-conjugated secondary antibody was used to develop the signal for BAX (red) and endoG (green). Cell nuclei were counterstained with DAPI. Scale bar = 10 μm. B . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 5 min, 30 min, or 2, 6, and 12 h. Cells were fixed in 4% paraformaldehyde and stained for BAX and endoG. Quantitative analyses showing percentages of BAX-endoG co-localized cells in the total number of cells. C . An equal number of HEEC or Het1A cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. Quantitative analyses showing the ratio of endoG to BAX per cell. * indicates a significant change compared to the control. D . An equal number of HEEC or Het1A cells was seeded in 6-well plates and incubated with the complete medium (control) or the medium containing 5.0% ethanol (EtOH) for 2–12 h. Protein was extracted and analyzed by Western blotting for <t>BAX.</t> <t>GAPDH</t> was used as a loading control. E . Quantitative analyses of BAX expression against GAPDH
Mouse Monoclonal Anti Human Bax Antibody, 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/bax+mouse+monoclonal+antibody/Bax+Antibody/pmc12730891-56-38-44
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mouse monoclonal anti human bax antibody - by Bioz Stars, 2026-09
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2d2 mouse monoclonal antibody  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology 2d2 mouse monoclonal antibody
Alcohol exposure induces anastasis in esophageal epithelial cells. A . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for <t>BAX</t> and endoG. A Texas Red- or FITC-conjugated secondary antibody was used to develop the signal for BAX (red) and endoG (green). Cell nuclei were counterstained with DAPI. Scale bar = 10 μm. B . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 5 min, 30 min, or 2, 6, and 12 h. Cells were fixed in 4% paraformaldehyde and stained for BAX and endoG. Quantitative analyses showing percentages of BAX-endoG co-localized cells in the total number of cells. C . An equal number of HEEC or Het1A cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. Quantitative analyses showing the ratio of endoG to BAX per cell. * indicates a significant change compared to the control. D . An equal number of HEEC or Het1A cells was seeded in 6-well plates and incubated with the complete medium (control) or the medium containing 5.0% ethanol (EtOH) for 2–12 h. Protein was extracted and analyzed by Western blotting for <t>BAX.</t> <t>GAPDH</t> was used as a loading control. E . Quantitative analyses of BAX expression against GAPDH
2d2 Mouse Monoclonal Antibody, 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/bax+mouse+monoclonal+antibody/Bax+Antibody/pm41274283-259-14-18
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2d2 mouse monoclonal antibody - by Bioz Stars, 2026-09
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2 ig wb mouse monoclonal  (Proteintech)
96
Proteintech 2 ig wb mouse monoclonal
Alcohol exposure induces anastasis in esophageal epithelial cells. A . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for <t>BAX</t> and endoG. A Texas Red- or FITC-conjugated secondary antibody was used to develop the signal for BAX (red) and endoG (green). Cell nuclei were counterstained with DAPI. Scale bar = 10 μm. B . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 5 min, 30 min, or 2, 6, and 12 h. Cells were fixed in 4% paraformaldehyde and stained for BAX and endoG. Quantitative analyses showing percentages of BAX-endoG co-localized cells in the total number of cells. C . An equal number of HEEC or Het1A cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. Quantitative analyses showing the ratio of endoG to BAX per cell. * indicates a significant change compared to the control. D . An equal number of HEEC or Het1A cells was seeded in 6-well plates and incubated with the complete medium (control) or the medium containing 5.0% ethanol (EtOH) for 2–12 h. Protein was extracted and analyzed by Western blotting for <t>BAX.</t> <t>GAPDH</t> was used as a loading control. E . Quantitative analyses of BAX expression against GAPDH
2 Ig Wb Mouse Monoclonal, supplied by Proteintech, 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/bax+mouse+monoclonal+antibody/BAX+Antibody/pm41252671-117-11-16
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2 ig wb mouse monoclonal - by Bioz Stars, 2026-09
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anti bax mouse monoclonal antibody  (Proteintech)
96
Proteintech anti bax mouse monoclonal antibody
Alcohol exposure induces anastasis in esophageal epithelial cells. A . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for <t>BAX</t> and endoG. A Texas Red- or FITC-conjugated secondary antibody was used to develop the signal for BAX (red) and endoG (green). Cell nuclei were counterstained with DAPI. Scale bar = 10 μm. B . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 5 min, 30 min, or 2, 6, and 12 h. Cells were fixed in 4% paraformaldehyde and stained for BAX and endoG. Quantitative analyses showing percentages of BAX-endoG co-localized cells in the total number of cells. C . An equal number of HEEC or Het1A cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. Quantitative analyses showing the ratio of endoG to BAX per cell. * indicates a significant change compared to the control. D . An equal number of HEEC or Het1A cells was seeded in 6-well plates and incubated with the complete medium (control) or the medium containing 5.0% ethanol (EtOH) for 2–12 h. Protein was extracted and analyzed by Western blotting for <t>BAX.</t> <t>GAPDH</t> was used as a loading control. E . Quantitative analyses of BAX expression against GAPDH
Anti Bax Mouse Monoclonal Antibody, supplied by Proteintech, 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/bax+mouse+monoclonal+antibody/BAX+Antibody/pm41242572-117-1-20
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anti bax mouse monoclonal antibody - by Bioz Stars, 2026-09
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mouse monoclonal antibodies against bax  (Cell Signaling Technology Inc)
86
Cell Signaling Technology Inc mouse monoclonal antibodies against bax
Alcohol exposure induces anastasis in esophageal epithelial cells. A . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for <t>BAX</t> and endoG. A Texas Red- or FITC-conjugated secondary antibody was used to develop the signal for BAX (red) and endoG (green). Cell nuclei were counterstained with DAPI. Scale bar = 10 μm. B . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 5 min, 30 min, or 2, 6, and 12 h. Cells were fixed in 4% paraformaldehyde and stained for BAX and endoG. Quantitative analyses showing percentages of BAX-endoG co-localized cells in the total number of cells. C . An equal number of HEEC or Het1A cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. Quantitative analyses showing the ratio of endoG to BAX per cell. * indicates a significant change compared to the control. D . An equal number of HEEC or Het1A cells was seeded in 6-well plates and incubated with the complete medium (control) or the medium containing 5.0% ethanol (EtOH) for 2–12 h. Protein was extracted and analyzed by Western blotting for <t>BAX.</t> <t>GAPDH</t> was used as a loading control. E . Quantitative analyses of BAX expression against GAPDH
Mouse Monoclonal Antibodies Against Bax, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse monoclonal antibodies against bax - by Bioz Stars, 2026-09
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Alcohol exposure induces anastasis in esophageal epithelial cells. A . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. A Texas Red- or FITC-conjugated secondary antibody was used to develop the signal for BAX (red) and endoG (green). Cell nuclei were counterstained with DAPI. Scale bar = 10 μm. B . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 5 min, 30 min, or 2, 6, and 12 h. Cells were fixed in 4% paraformaldehyde and stained for BAX and endoG. Quantitative analyses showing percentages of BAX-endoG co-localized cells in the total number of cells. C . An equal number of HEEC or Het1A cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. Quantitative analyses showing the ratio of endoG to BAX per cell. * indicates a significant change compared to the control. D . An equal number of HEEC or Het1A cells was seeded in 6-well plates and incubated with the complete medium (control) or the medium containing 5.0% ethanol (EtOH) for 2–12 h. Protein was extracted and analyzed by Western blotting for BAX. GAPDH was used as a loading control. E . Quantitative analyses of BAX expression against GAPDH

Journal: BMC Molecular and Cell Biology

Article Title: Alcohol exposure induces ferroptosis-dominated programmed cell death in esophageal epithelial cells

doi: 10.1186/s12860-026-00589-5

Figure Lengend Snippet: Alcohol exposure induces anastasis in esophageal epithelial cells. A . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. A Texas Red- or FITC-conjugated secondary antibody was used to develop the signal for BAX (red) and endoG (green). Cell nuclei were counterstained with DAPI. Scale bar = 10 μm. B . An equal number of HEEC cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 5 min, 30 min, or 2, 6, and 12 h. Cells were fixed in 4% paraformaldehyde and stained for BAX and endoG. Quantitative analyses showing percentages of BAX-endoG co-localized cells in the total number of cells. C . An equal number of HEEC or Het1A cells was seeded on coverslips and incubated with complete medium (control) or medium containing 5.0% ethanol for 2–12 h. Cells were fixed in 4% paraformaldehyde and double-stained for BAX and endoG. Quantitative analyses showing the ratio of endoG to BAX per cell. * indicates a significant change compared to the control. D . An equal number of HEEC or Het1A cells was seeded in 6-well plates and incubated with the complete medium (control) or the medium containing 5.0% ethanol (EtOH) for 2–12 h. Protein was extracted and analyzed by Western blotting for BAX. GAPDH was used as a loading control. E . Quantitative analyses of BAX expression against GAPDH

Article Snippet: The following primary antibodies were used: Beclin-1 (Origene, #TA502643), PCNA, CASP1 (Abcam, #ab179515), CASP3 (Santa Cruz Biotechnology, #sc-271759), CASP8 (Origene, #TA374288), CASP9 (Origene, #TA4227045), endoG, GPX4 (Origene, #TA423164M), GSDMD, IL-1β (Santa Cruz Biotechnology, #sc-12742), MLKL, phosphor-MLKL (Abcam, #ab196436), SLC7A11 (Origene, #TA423232), LC3B, BAX, GAPDH (OriGene, #TA800894), and β-actin (Santa Cruz Biotechnology, Inc. #sc-69879).

Techniques: Incubation, Control, Staining, Western Blot, Expressing