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mouse anti-proliferating cell nuclear antigen (pcna) antibody  (Boster Bio)


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    Structured Review

    Boster Bio mouse anti-proliferating cell nuclear antigen (pcna) antibody
    Western blotting results of different composite hydrogels. The results of western blotting assay revealed no significant differences in cell protein expression among the different groups (P>0.05). <t>PCNA,</t> proliferating cell nuclear antigen; CS/β-GP, chitosan/β-glycerophosphate; TiO 2 NPs, titanium dioxide nanoparticles.
    Mouse Anti Proliferating Cell Nuclear Antigen (Pcna) Antibody, supplied by Boster Bio, 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/result/mouse anti-proliferating cell nuclear antigen (pcna) antibody/product/Boster Bio
    Average 90 stars, based on 1 article reviews
    mouse anti-proliferating cell nuclear antigen (pcna) antibody - by Bioz Stars, 2026-02
    90/100 stars

    Images

    1) Product Images from "TiO 2 NPs improve ultrasound response: CS/β-GP/TiO 2 NP hydrogel enabling on-demand administration"

    Article Title: TiO 2 NPs improve ultrasound response: CS/β-GP/TiO 2 NP hydrogel enabling on-demand administration

    Journal: Biomedical Reports

    doi: 10.3892/br.2025.2020

    Western blotting results of different composite hydrogels. The results of western blotting assay revealed no significant differences in cell protein expression among the different groups (P>0.05). PCNA, proliferating cell nuclear antigen; CS/β-GP, chitosan/β-glycerophosphate; TiO 2 NPs, titanium dioxide nanoparticles.
    Figure Legend Snippet: Western blotting results of different composite hydrogels. The results of western blotting assay revealed no significant differences in cell protein expression among the different groups (P>0.05). PCNA, proliferating cell nuclear antigen; CS/β-GP, chitosan/β-glycerophosphate; TiO 2 NPs, titanium dioxide nanoparticles.

    Techniques Used: Western Blot, Expressing, Titanium Dioxide



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    Boster Bio mouse anti-proliferating cell nuclear antigen (pcna) antibody
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    Proteintech mouse anti proliferating cell nuclear antigen pcna antibody
    (a-d) 10 days taurine supplementation to the Cdo KO mice (KO+Tau) increases the taurine level (a), the number of uterine glands marked by Foxa2 (b, c) and Foxa2 mRNA levels (d) in the uterine tissue. (e) Western Blot detection and analysis of <t>PCNA</t> protein levels in the uteri of the WT, Cdo KO and KO + Tau mice (n ≥ 3). (f) Western blot detection of BAX/BCL2 protein levels (up) and the analysis of BAX/BCL2 ration (down) in the uteri of the WT, Cdo KO and KO + Tau mice. WT: wild type. KO: Cdo KO. PND: Postnatal day. Scale bar represents 20 μm. *P < 0.05, **P < 0.01, ***P < 0.001.
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    Boster Bio mouse monoclonal anti pcna
    (a-d) 10 days taurine supplementation to the Cdo KO mice (KO+Tau) increases the taurine level (a), the number of uterine glands marked by Foxa2 (b, c) and Foxa2 mRNA levels (d) in the uterine tissue. (e) Western Blot detection and analysis of <t>PCNA</t> protein levels in the uteri of the WT, Cdo KO and KO + Tau mice (n ≥ 3). (f) Western blot detection of BAX/BCL2 protein levels (up) and the analysis of BAX/BCL2 ration (down) in the uteri of the WT, Cdo KO and KO + Tau mice. WT: wild type. KO: Cdo KO. PND: Postnatal day. Scale bar represents 20 μm. *P < 0.05, **P < 0.01, ***P < 0.001.
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    Image Search Results


    Western blotting results of different composite hydrogels. The results of western blotting assay revealed no significant differences in cell protein expression among the different groups (P>0.05). PCNA, proliferating cell nuclear antigen; CS/β-GP, chitosan/β-glycerophosphate; TiO 2 NPs, titanium dioxide nanoparticles.

    Journal: Biomedical Reports

    Article Title: TiO 2 NPs improve ultrasound response: CS/β-GP/TiO 2 NP hydrogel enabling on-demand administration

    doi: 10.3892/br.2025.2020

    Figure Lengend Snippet: Western blotting results of different composite hydrogels. The results of western blotting assay revealed no significant differences in cell protein expression among the different groups (P>0.05). PCNA, proliferating cell nuclear antigen; CS/β-GP, chitosan/β-glycerophosphate; TiO 2 NPs, titanium dioxide nanoparticles.

    Article Snippet: The following materials were used: i) CS powder (95% deacetylation degree; cat. no. C105799; Aladdin Scientific Corp.), ii) β-GP pentahydrate (cat. no. D106347; Aladdin Scientific Corp.), iii) sodium fluorescein (NaF; cat. no. F105615; Aladdin), iv) TiO 2 NPs (20-40 nm; cat. no. NM000800; Beijing Solarbio Science & Technology Co., Ltd.), v) L929 murine fibroblast cells (cat. no. KGG1306-1), vi) RPMI-1640 medium (containing newborn calf serum, double antibiotics; cat. no. KGL1509-500), vii) Cell Counting Kit-8 (CCK-8) cell proliferation assay kit (cat. no. KGA9305-500), viii) LIVE/DEAD cell viability assay kit (cat. no. KGA9501-1000), ix) bovine serum albumin (BSA) (standard grade, heat-treated) (cat. no. KGL2314-10), x) bicinchoninic acid (BCA) protein quantification assay kit (cat. no. KGB2101-250), all from Jiangsu KeyGen Biotech Co., Ltd., xi) mouse anti-proliferating cell nuclear antigen (PCNA) antibody (1:1,000; cat. no. BM0104) and xii) goat anti-mouse IgG/HRP antibody (1:10,000; cat. no. BA1056) both from Boster Biological Technology Co. Ltd.

    Techniques: Western Blot, Expressing, Titanium Dioxide

    (a-d) 10 days taurine supplementation to the Cdo KO mice (KO+Tau) increases the taurine level (a), the number of uterine glands marked by Foxa2 (b, c) and Foxa2 mRNA levels (d) in the uterine tissue. (e) Western Blot detection and analysis of PCNA protein levels in the uteri of the WT, Cdo KO and KO + Tau mice (n ≥ 3). (f) Western blot detection of BAX/BCL2 protein levels (up) and the analysis of BAX/BCL2 ration (down) in the uteri of the WT, Cdo KO and KO + Tau mice. WT: wild type. KO: Cdo KO. PND: Postnatal day. Scale bar represents 20 μm. *P < 0.05, **P < 0.01, ***P < 0.001.

    Journal: PLOS One

    Article Title: Cysteine dioxygenase knockout and taurine deficiency impair mouse uterine adenogenesis by inhibiting epithelial cell proliferation and enhancing apoptosis

    doi: 10.1371/journal.pone.0329503

    Figure Lengend Snippet: (a-d) 10 days taurine supplementation to the Cdo KO mice (KO+Tau) increases the taurine level (a), the number of uterine glands marked by Foxa2 (b, c) and Foxa2 mRNA levels (d) in the uterine tissue. (e) Western Blot detection and analysis of PCNA protein levels in the uteri of the WT, Cdo KO and KO + Tau mice (n ≥ 3). (f) Western blot detection of BAX/BCL2 protein levels (up) and the analysis of BAX/BCL2 ration (down) in the uteri of the WT, Cdo KO and KO + Tau mice. WT: wild type. KO: Cdo KO. PND: Postnatal day. Scale bar represents 20 μm. *P < 0.05, **P < 0.01, ***P < 0.001.

    Article Snippet: The membrane was blocked with 5% (w/v) nonfat dry milk in 0.05 mol/L pH 7.4 Tris buffered saline (TBS) for 1 h and incubated with rabbit anti-CDO antibody (ab53436, abcam, Cambridge, UK; 1:2000), mouse anti- proliferating cell nuclear antigen (PCNA) antibody (60097–1-Ig, Proteintech Group, Inc., IL, USA; 1:2000), rabbit anti-BCL2-Associated X Protein (BAX) antibody ( T40051 , Abmart Shanghai Co.,Ltd., China, 1:2000), rabbit anti-BCL2-Associated X Protein (BAX) antibody (ab182858, abcam, Cambridge, UK; 1:2000), and internal control rabbit anti-Tubulin antibody (K006154P, Beijing Solarbio Science & Technology Co.,Ltd., China, 1:2000) overnight at 4°C.

    Techniques: Western Blot