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mouse monoclonal anti pcna  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc mouse monoclonal anti pcna
    Mouse Monoclonal Anti Pcna, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1094 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+monoclonal+anti+pcna/PCNA+Mouse+mAb/pm41896623-289-24-29
    Average 96 stars, based on 1094 article reviews
    mouse monoclonal anti pcna - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    other:

    Article Title: Integrative modeling uncovers p21-driven drug resistance and prioritizes therapies for PIK3CA-mutant breast cancer
    Article Snippet: Mouse monoclonal anti-PCNA (clone PC10) 1:1000 dilution , Cell Signaling Technology , Cat#2586; RRID:AB_2160343.

    Article Title: circGlis3 promotes β-cell dysfunction by binding to heterogeneous nuclear ribonucleoprotein F and encoding Glis3-348aa protein
    Article Snippet: Mouse monoclonal anti-PCNA , Cell Signaling Technology , Cat# 2586; RRID: AB_2160343.

    Article Title: KLF2 controls proliferation and apoptosis of human spermatogonial stem cells via targeting GJA1
    Article Snippet: Mouse monoclonal anti-PCNA , Cell Signaling Technology , Cat# 2586; RRID: AB_2160343.

    Article Title: Hericium erinaceus extracts promote neuronal differentiation and excitability through nootropic metabolite activity.
    Article Snippet: USA), the mouse polyclonal antibody anti-Nav (Neuromab, USA), the rabbit polyclonal antibody anti-Synaptotagmin-1,2 (Abcam, Cambridge, UK), diluted 1:200, 1:200, 1:200, 1:250, 1:200 in PBS (Merck, Italy) for 1 hour at RT in a dark, moist chamber.

    Expressing:

    Article Title: Altered fatty acid metabolism rewires cholangiocarcinoma stemness features
    Article Snippet: Immunohistochemistry was performed using the Leica BOND-MAXTM automated system (Leica Microsystems). .. The expression of mouse monoclonal anti-PCNA (#2586, 1:8000, Cell Signaling Technology) was evaluated. .. Slides were developed with 3′3-diaminobenzidine DAB (Leica Microsystems) and counterstained with hematoxylin.

    Article Title: Altered fatty acid metabolism rewires cholangiocarcinoma stemness features
    Article Snippet: Immunohistochemistry was performed using the Leica BOND-MAXTM automated system (Leica Microsystems). .. The expression of mouse monoclonal anti-PCNA (#2586, 1:8000, Cell Signaling Technology) was evaluated. .. Slides were developed with 3′3-diaminobenzidine DAB (Leica Microsystems) and counterstained with hematoxylin.

    Immunostaining:

    Article Title: Lnc956-TRIM28-HSP90B1 complex on replication forks promotes CMG helicase retention to ensure stem cell genomic stability and embryogenesis
    Article Snippet: .. Antibodies Source Dilution Mouse monoclonal anti-BrdU (clone B44), also used for immunostaining of IdU BD Biosciences; Cat#347580 1:500 (IF) Rat monoclonal anti-BrdU (clone BU1/75), also used for immunostaining of CIdU Novus; Cat#NB500-169 1:1000 (IF) Mouse monoclonal anti-PCNA (clone PC10) Cell Signaling Technology; Cat#2586 1:1000 (IB) Ds DNA maker (HYB331-01) Santa Cruz; Cat#sc-58749 1:1000 (IB) Mouse monoclonal anti-GAPDH Sangon Biotech; Cat#D190090 1:1000 (IB) Rabbit polyclonal anti-γ-H2AX (clone 20E3) Cell Signaling Technology; Cat#9718 1:1000 (IB) CHK1 Mouse monoclonal antibody (clone 2G1D5) Cell Signaling Technology; Cat#2360S 1:1000 (IB) Rabbit anti-p-ATR (Ser428) Cell Signaling Technology; Cat#2853S 1:1000 (IB) Rabbit polyclonal anti-ATR Cell Signaling Technology; Cat#2790S 1:1000 (IB) P-CHK1(S345) Rabbit monoclonal antibody(133D3) Cell Signaling Technology; Cat#2348S 1:1000 (IB) Anti-RPA32/RPA2 antibody Abcam; Cat#ab76420 1:1000(IB) Anti-RPA32/RPA2 (phosphoS33) antibody Abcam; Cat#ab211877 1:1000(IB) β-Actin mouse antibody Abclonal; Cat#AC004 1:10000 (IB) Histone H3 (D1H2) XP® Rabbit mAb Cell Signaling Technology; Cat#4499S 1:1000(IB) Anti-KAP1(TRIM28) antibody Abcam; Cat#ab10483 1:1000 (IB) Recombinant Anti-MCM5 antibody (clone EP2683Y) Abcam; Cat#ab75975 1:1000 (IB) Recombinant Anti-MCM6 antibody (clone EPR17686) Abcam; Cat#ab201683 1:1000 (IB) MCM7 XP Rabbit mAb (clone D10A11) Cell Signaling Technology; Cat#3735T 1:1000 (IB) Recombinant Anti-HSP90B1 (GRP94) antibody Abcam; Cat#ab238126 1:1000 (IB) CDC45 Rabbit mAb (clone D7G6) Cell Signaling Technology; Cat#11881s 1:1000 (IB) Recombinant Anti-PSF1 antibody (clone EPR13359) Abcam; ab181112 1:1000 (IB) Rabbit monoclonal anti-K63-linkage Specific Polyubiquitin (clone D7A11) Cell Signaling Technology; Cat#5621 1:1000 (IB) K48-linkage Specific Polyubiquitin (cloneD9D5) Rabbit mAb Cell Signaling Technology; Cat#8081 1:1000 (IB) HP1β XP® Rabbit mAb(cloneD2F2) Cell Signaling Technology; Cat#8676 1:500 (IF) Goat anti-Mouse IgG (H+L) Secondary Antibody, Alexa Fluor 488 Thermo Fisher Scientific; Cat#A-11029 1:500 (IF) Goat anti-Rat IgG Secondary Antibody, Alexa Fluor Cy3 Thermo Fisher Scientific; Cat#A-10522 1:500 (IF) Goat anti-Rat IgG (H+L) Secondary Antibody, Alexa Fluor 647 Thermo Fisher Scientific; Cat#A-21247 1:500 (IF) 30 Goat anti-Rabbit IgG (H+L) Secondary Antibody, Alexa Fluor 488 Thermo Fisher Scientific; Cat#A-32731 1:500 (IF) Goat anti-Mouse IgG (H+L) Secondary Antibody, HRP Thermo Fisher Scientific; Cat#31430 1:5000 (IB) Goat anti-Rabbit IgG (H+L) Secondary Antibody, HRP Thermo Fisher Scientific; Cat#31460 1:5000 (IB) Dataset S1. ..

    Recombinant:

    Article Title: Lnc956-TRIM28-HSP90B1 complex on replication forks promotes CMG helicase retention to ensure stem cell genomic stability and embryogenesis
    Article Snippet: .. Antibodies Source Dilution Mouse monoclonal anti-BrdU (clone B44), also used for immunostaining of IdU BD Biosciences; Cat#347580 1:500 (IF) Rat monoclonal anti-BrdU (clone BU1/75), also used for immunostaining of CIdU Novus; Cat#NB500-169 1:1000 (IF) Mouse monoclonal anti-PCNA (clone PC10) Cell Signaling Technology; Cat#2586 1:1000 (IB) Ds DNA maker (HYB331-01) Santa Cruz; Cat#sc-58749 1:1000 (IB) Mouse monoclonal anti-GAPDH Sangon Biotech; Cat#D190090 1:1000 (IB) Rabbit polyclonal anti-γ-H2AX (clone 20E3) Cell Signaling Technology; Cat#9718 1:1000 (IB) CHK1 Mouse monoclonal antibody (clone 2G1D5) Cell Signaling Technology; Cat#2360S 1:1000 (IB) Rabbit anti-p-ATR (Ser428) Cell Signaling Technology; Cat#2853S 1:1000 (IB) Rabbit polyclonal anti-ATR Cell Signaling Technology; Cat#2790S 1:1000 (IB) P-CHK1(S345) Rabbit monoclonal antibody(133D3) Cell Signaling Technology; Cat#2348S 1:1000 (IB) Anti-RPA32/RPA2 antibody Abcam; Cat#ab76420 1:1000(IB) Anti-RPA32/RPA2 (phosphoS33) antibody Abcam; Cat#ab211877 1:1000(IB) β-Actin mouse antibody Abclonal; Cat#AC004 1:10000 (IB) Histone H3 (D1H2) XP® Rabbit mAb Cell Signaling Technology; Cat#4499S 1:1000(IB) Anti-KAP1(TRIM28) antibody Abcam; Cat#ab10483 1:1000 (IB) Recombinant Anti-MCM5 antibody (clone EP2683Y) Abcam; Cat#ab75975 1:1000 (IB) Recombinant Anti-MCM6 antibody (clone EPR17686) Abcam; Cat#ab201683 1:1000 (IB) MCM7 XP Rabbit mAb (clone D10A11) Cell Signaling Technology; Cat#3735T 1:1000 (IB) Recombinant Anti-HSP90B1 (GRP94) antibody Abcam; Cat#ab238126 1:1000 (IB) CDC45 Rabbit mAb (clone D7G6) Cell Signaling Technology; Cat#11881s 1:1000 (IB) Recombinant Anti-PSF1 antibody (clone EPR13359) Abcam; ab181112 1:1000 (IB) Rabbit monoclonal anti-K63-linkage Specific Polyubiquitin (clone D7A11) Cell Signaling Technology; Cat#5621 1:1000 (IB) K48-linkage Specific Polyubiquitin (cloneD9D5) Rabbit mAb Cell Signaling Technology; Cat#8081 1:1000 (IB) HP1β XP® Rabbit mAb(cloneD2F2) Cell Signaling Technology; Cat#8676 1:500 (IF) Goat anti-Mouse IgG (H+L) Secondary Antibody, Alexa Fluor 488 Thermo Fisher Scientific; Cat#A-11029 1:500 (IF) Goat anti-Rat IgG Secondary Antibody, Alexa Fluor Cy3 Thermo Fisher Scientific; Cat#A-10522 1:500 (IF) Goat anti-Rat IgG (H+L) Secondary Antibody, Alexa Fluor 647 Thermo Fisher Scientific; Cat#A-21247 1:500 (IF) 30 Goat anti-Rabbit IgG (H+L) Secondary Antibody, Alexa Fluor 488 Thermo Fisher Scientific; Cat#A-32731 1:500 (IF) Goat anti-Mouse IgG (H+L) Secondary Antibody, HRP Thermo Fisher Scientific; Cat#31430 1:5000 (IB) Goat anti-Rabbit IgG (H+L) Secondary Antibody, HRP Thermo Fisher Scientific; Cat#31460 1:5000 (IB) Dataset S1. ..

    Incubation:

    Article Title: ALDOB K87 lactylation drives mitochondrial fission and metabolic reprogramming in pulmonary hypertension.
    Article Snippet: .. The sections were blocked with 5% bovine serum albumin containing 0.3% Triton X-100 at 37°C for 1 h before sequential incubation with primary antibodies: mouse monoclonal anti-PCNA (#2586, 1:200; CST, ) at 4°C overnight, followed by rabbit polyclonal anti-α-SMA (#19245, 1:500; CST, ) at 37°C for 2 h. Species-matched secondary AR TI CL E IN P RE SS antibodies (Alexa Fluor 488-conjugated anti-mouse IgG and Cy3-conjugated anti-rabbit IgG, both at 1:1000 dilution) were applied at 37°C for 1 h each with light protection, interspersed with PBS washes. ..



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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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    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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    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