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monoclonal rabbit anti cdk2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc monoclonal rabbit anti cdk2
    Monoclonal Rabbit Anti Cdk2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 779 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/monoclonal+rabbit+anti+cdk2/CDK2+Rabbit+mAb/bio_rxiv__64898__2025__12__30__697000-190-41-71
    Average 96 stars, based on 779 article reviews
    monoclonal rabbit anti cdk2 - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Western Blot:

    Article Title: Translational control of AMPK activity in melanoma
    Article Snippet: .. Primary antibodies used for western blot: monoclonal rabbit anti-phospho-AMPK (2535), monoclonal rabbit anti-AMPK (2532), monoclonal rabbit anti-phospho-ERK1/2 (#4370), polyclonal rabbit anti-ERK1/2 (#9102), monoclonal rabbit anti-EGR1 (#4153), monoclonal rabbit anti-eIF4A (#2013), monoclonal rabbit anti-eIF4E, polyclonal rabbit anti-eIF4G (#2498), monoclonal mouse anti-CDK1 (9116), monoclonal rabbit anti-CDK2 (2546), monoclonal rabbit anti-LAMTOR1 (8975), monoclonal rabbit anti-LKB1 (3047), monoclonal rabbit anti-MO25 (2716), monoclonal rabbit anti-MLK3 (2817), monoclonal rabbit anti-PP2AAsubunit (2041), monoclonal rabbit anti-TYMS (5449) purchased from Cell Signaling Technologies and monoclonal mouse anti-DUSP6 (sc-377070), monoclonal mouse anti-vinculin (sc-73614), monoclonal mouse anti-CAMKKβ (sc-271674), monoclonal mouse anti-GAPDH (sc-47724) purchased from Santa Cruz Biotechnology. ..



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    Cg CHIP inhibits granulocyte proliferation. ( A ) Representative flow cytometry peak diagrams show the proliferation rate of gated EdU labeling agranulocytes in total agranulocytes. ( B ) The bar graph shows the proliferation rate of agranulocytes ( n = 3). ( C ) Representative flow cytometry peak diagrams showing the proliferation rate of gated EdU labeling granulocytes in total granulocytes. ( D ) The bar graph shows the proliferation rate of granulocytes ( n = 3). * p < 0.05, determined by a two-tailed Student’s t test. ( E ) Schematic of granulocyte isolation for cell cycle and Western blotting analyses. ( F ) The percentage changes of granulocytes in different cell cycle phases. ( G ) The bar graph shows the percentage of agranulocytes in different cell cycle phases ( n = 3). Error bars show mean ± standard deviation ( n = 3). p -values, * p < 0.05, ** p < 0.01, were calculated using a one-way ANOVA with Dunnett’s correction for multiple comparisons. ( H , I ) Protein expression levels of proliferative genes Cg Cyclin B1 and Cg <t>CDK2</t> in granulocytes. β-Tubulin was used as an internal control. Error bars show mean ± standard deviation ( n = 3). The data shown are representative of three independent experiments. * p < 0.05, ** p < 0.01, determined by a two-tailed Student’s t test.
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    Image Search Results


    Cg CHIP inhibits granulocyte proliferation. ( A ) Representative flow cytometry peak diagrams show the proliferation rate of gated EdU labeling agranulocytes in total agranulocytes. ( B ) The bar graph shows the proliferation rate of agranulocytes ( n = 3). ( C ) Representative flow cytometry peak diagrams showing the proliferation rate of gated EdU labeling granulocytes in total granulocytes. ( D ) The bar graph shows the proliferation rate of granulocytes ( n = 3). * p < 0.05, determined by a two-tailed Student’s t test. ( E ) Schematic of granulocyte isolation for cell cycle and Western blotting analyses. ( F ) The percentage changes of granulocytes in different cell cycle phases. ( G ) The bar graph shows the percentage of agranulocytes in different cell cycle phases ( n = 3). Error bars show mean ± standard deviation ( n = 3). p -values, * p < 0.05, ** p < 0.01, were calculated using a one-way ANOVA with Dunnett’s correction for multiple comparisons. ( H , I ) Protein expression levels of proliferative genes Cg Cyclin B1 and Cg CDK2 in granulocytes. β-Tubulin was used as an internal control. Error bars show mean ± standard deviation ( n = 3). The data shown are representative of three independent experiments. * p < 0.05, ** p < 0.01, determined by a two-tailed Student’s t test.

    Journal: Cells

    Article Title: E3 Ubiquitin Ligase CHIP Inhibits Haemocyte Proliferation and Differentiation via the Ubiquitination of Runx in the Pacific Oyster

    doi: 10.3390/cells13181535

    Figure Lengend Snippet: Cg CHIP inhibits granulocyte proliferation. ( A ) Representative flow cytometry peak diagrams show the proliferation rate of gated EdU labeling agranulocytes in total agranulocytes. ( B ) The bar graph shows the proliferation rate of agranulocytes ( n = 3). ( C ) Representative flow cytometry peak diagrams showing the proliferation rate of gated EdU labeling granulocytes in total granulocytes. ( D ) The bar graph shows the proliferation rate of granulocytes ( n = 3). * p < 0.05, determined by a two-tailed Student’s t test. ( E ) Schematic of granulocyte isolation for cell cycle and Western blotting analyses. ( F ) The percentage changes of granulocytes in different cell cycle phases. ( G ) The bar graph shows the percentage of agranulocytes in different cell cycle phases ( n = 3). Error bars show mean ± standard deviation ( n = 3). p -values, * p < 0.05, ** p < 0.01, were calculated using a one-way ANOVA with Dunnett’s correction for multiple comparisons. ( H , I ) Protein expression levels of proliferative genes Cg Cyclin B1 and Cg CDK2 in granulocytes. β-Tubulin was used as an internal control. Error bars show mean ± standard deviation ( n = 3). The data shown are representative of three independent experiments. * p < 0.05, ** p < 0.01, determined by a two-tailed Student’s t test.

    Article Snippet: The other antibodies used for Western blotting were monoclonal antibodies, including rabbit monoclonal antibodies against PCNA (1:1000, Cell Signaling Technology, Boston, MA, USA), rabbit monoclonal antibodies against Cyclin B1 (1:1000, ABclonal, Wuhan, China), rabbit monoclonal antibodies against CDK2 (1:1000, Cell Signaling Technology, Boston, MA, USA), mouse monoclonal antibodies against Histone H3 (1:5000, Proteintech, Chicago, IL, USA), and HRP-conjugated rabbit monoclonal against beta-Tubulin (1:10,000, Proteintech, Chicago, IL, USA).

    Techniques: Flow Cytometry, Labeling, Two Tailed Test, Isolation, Western Blot, Standard Deviation, Expressing, Control

    Journal: NPJ Precision Oncology

    Article Title: Integrative modeling uncovers p21-driven drug resistance and prioritizes therapies for PIK3CA-mutant breast cancer

    doi: 10.1038/s41698-024-00496-y

    Figure Lengend Snippet:

    Article Snippet: Rabbit monoclonal anti-CDK2 (clone 78B2) 1:1000 dilution , Cell Signaling Technology , Cat# 2546; RRID:AB_2276129.

    Techniques:

    Journal: Cell Reports Medicine

    Article Title: Co-targeting RANK pathway treats and prevents acquired resistance to CDK4/6 inhibitors in luminal breast cancer

    doi: 10.1016/j.xcrm.2023.101120

    Figure Lengend Snippet:

    Article Snippet: Rabbit monoclonal anti CDK2 (78B2) , Cell Signaling , Cat#2546; RRID:AB_2276129.

    Techniques: Recombinant, Control, shRNA, Blocking Assay, Alamar Blue Assay, Flow Cytometry, Isolation, cDNA Synthesis, Bicinchoninic Acid Protein Assay, TUNEL Assay, Enzyme-linked Immunosorbent Assay, Gene Expression, Western Blot, Software