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mouse monoclonal anti pcna  (Proteintech)


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    Structured Review

    Proteintech mouse monoclonal anti pcna
    Mouse Monoclonal Anti Pcna, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 43 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+monoclonal+anti+pcna/MCM7+Antibody/pm41730953-53-44-48
    Average 93 stars, based on 43 article reviews
    mouse monoclonal anti pcna - by Bioz Stars, 2026-11
    93/100 stars

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    Related Articles

    other:

    Article Title: Claudin18.2 promote gastric cancer proliferation by activating MCM2/5.
    Article Snippet: AR TIC LE IN PR ES S ARTICLE IN PRESS (Thr202/Tyr204) (#80031-1-RR; Proteintech), rabbit polyclonal antiMCM2 (#10513-1-AP; Proteintech), rabbit polyclonal anti-MCM3 (#15597-1-AP; Proteintech), mouse monoclonal anti-MCM4 (#67103-1-lg; Proteintech), rabbit polyclonal anti-MCM5 (#11703- 1-AP; Proteintech), mouse monoclonal anti-MCM6 (#67989-1-lg; Proteintech), rabbit polyclonal anti-MCM7 (#11225-1-AP; Proteintech), mouse monoclonal anti-PCNA (#60097-1-lg; Proteintech), mouse monoclonal anti-Ki-67 (#9449S; CST), mouse monoclonal anti-β-Tubulin (#86298; CST), rabbit polyclonal antiATP1A1 (#14418-1-AP; Proteintech), mouse monoclonal anti-CDK1 (#A11420; ABclonal), rabbit polyclonal anti-Phospho-CDK1 (T161) (#AP0324; ABclonal), and rabbit polyclonal anti-Phospho-MCM2 (S139) (#AP1192; ABclonal).

    Recombinant:

    Article Title: Claudin18.2 promote gastric cancer proliferation by activating MCM2/5
    Article Snippet: .. The following antibodies were used: rabbit monoclonal anti-CLDN18.2 (ab222512; Abcam), mouse monoclonal anti-AKT (#60203-2-lg; Proteintech), mouse monoclonal anti-Phospho-AKT (Ser473) (#66444-1-lg; Proteintech), rabbit monoclonal anti-ERK1/2 (#4695; CST), rabbit recombinant anti-Phospho-ERK1/2 (Thr202/Tyr204) (#80031-1-RR; Proteintech), rabbit polyclonal anti-MCM2 (#10513-1-AP; Proteintech), rabbit polyclonal anti-MCM3 (#15597-1-AP; Proteintech), mouse monoclonal anti-MCM4 (#67103-1-lg; Proteintech), rabbit polyclonal anti-MCM5 (#11703-1-AP; Proteintech), mouse monoclonal anti-MCM6 (#67989-1-lg; Proteintech), rabbit polyclonal anti-MCM7 (#11225-1-AP; Proteintech), mouse monoclonal anti-PCNA (#60097-1-lg; Proteintech), mouse monoclonal anti-Ki-67 (#9449S; CST), mouse monoclonal anti-β-Tubulin (#86298; CST), rabbit polyclonal anti-ATP1A1 (#14418-1-AP; Proteintech), mouse monoclonal anti-CDK1 (#A11420; ABclonal), rabbit polyclonal anti-Phospho-CDK1 (T161) (#AP0324; ABclonal), and rabbit polyclonal anti-Phospho-MCM2 (S139) (#AP1192; ABclonal). ..

    Incubation:

    Article Title: Early Histone Deacetylase Inhibition Mitigates Ischemia/Reperfusion Brain Injury by Reducing Microglia Activation and Modulating Their Phenotype
    Article Snippet: .. Then, sections were incubated with the rabbit polyclonal anti-TMEM119 (1:200, 27585-1-AP, Proteintech), mouse monoclonal anti-PCNA (1:50, 60097-1-Ig, Proteintech), mouse monoclonal anti-IL-1β (1:200, sc-52012, Santa Cruz), rabbit monoclonal anti-Arg1 (1:500, 93668, Cell Signaling Technology), and Alexa Fluor 488 or 555-conjugated secondary antibodies (1:500, Cell Signaling Technology). .. Nuclei were counterstained with DAPI (1 μg/mL, Sigma).



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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 <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
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    Santa Cruz Biotechnology monoclonal mouse anti pcna
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    Leinco Technologies mouse monoclonal anti pcna
    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
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    Proteintech mouse monoclonal anti pcna
    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 Pcna, supplied by Proteintech, 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/mouse+monoclonal+anti+pcna/MCM7+Antibody/pm41730953-53-44-48
    Average 93 stars, based on 1 article reviews
    mouse monoclonal anti pcna - by Bioz Stars, 2026-11
    93/100 stars
      Buy from Supplier

    Image Search Results


    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