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rabbit polyclonal antibodies (abs) against cyclin d1  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit polyclonal antibodies (abs) against cyclin d1
    Rabbit Polyclonal Antibodies (Abs) Against Cyclin D1, supplied by Cell Signaling Technology Inc, 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/rabbit polyclonal antibodies (abs) against cyclin d1/product/Cell Signaling Technology Inc
    Average 90 stars, based on 1 article reviews
    rabbit polyclonal antibodies (abs) against cyclin d1 - by Bioz Stars, 2026-02
    90/100 stars

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    rabbit polyclonal antibodies (abs) against cyclin d1  (Cell Signaling Technology Inc)
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    Cell Signaling Technology Inc rabbit polyclonal antibodies (abs) against cyclin d1
    Rabbit Polyclonal Antibodies (Abs) Against Cyclin D1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rabbit polyclonal antibody against cyclin d1 ab 3  (Thermo Fisher)
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    Thermo Fisher rabbit polyclonal antibody against cyclin d1 ab 3
    Western blot analysis of cell cycle proteins from mouse epidermis. Protein lysates of epidermis samples from K5-Myc, K5-Myc/CDK4−/−, K5-Myc/CDK4+/−, CDK4−/−, CDK4+/−, and wild-type siblings were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and blotted onto a nitrocellulose membrane. Primary antibodies against CDK4, CDK6, CDK2, <t>cyclin</t> <t>D1,</t> cyclin D2, cyclin A, and cyclin E were used for immunoblot analysis. Protein levels were quantified with a densitometer.
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    Western blot analysis of cell cycle proteins from mouse epidermis. Protein lysates of epidermis samples from K5-Myc, K5-Myc/CDK4−/−, K5-Myc/CDK4+/−, CDK4−/−, CDK4+/−, and wild-type siblings were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and blotted onto a nitrocellulose membrane. Primary antibodies against CDK4, CDK6, CDK2, cyclin D1, cyclin D2, cyclin A, and cyclin E were used for immunoblot analysis. Protein levels were quantified with a densitometer.

    Journal:

    Article Title: Lack of Cyclin-Dependent Kinase 4 Inhibits c- myc Tumorigenic Activities in Epithelial Tissues

    doi: 10.1128/MCB.24.17.7538-7547.2004

    Figure Lengend Snippet: Western blot analysis of cell cycle proteins from mouse epidermis. Protein lysates of epidermis samples from K5-Myc, K5-Myc/CDK4−/−, K5-Myc/CDK4+/−, CDK4−/−, CDK4+/−, and wild-type siblings were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and blotted onto a nitrocellulose membrane. Primary antibodies against CDK4, CDK6, CDK2, cyclin D1, cyclin D2, cyclin A, and cyclin E were used for immunoblot analysis. Protein levels were quantified with a densitometer.

    Article Snippet: The following antibodies were used: rabbit polyclonal antibodies against CDK4 (C22), CDK2 (M2), and CDK6 (C21) (all from Santa Cruz Biotechnology, Inc., Santa Cruz, Calif.); rabbit polyclonal antibody against cyclin D1 (Ab-3) (Lab Vision Corp./Neo Markers, Fremont, Calif.); and horseradish peroxidase-conjugated secondary antibody (Amersham Corp., Arlington Heights, Ill.).

    Techniques: Western Blot, Polyacrylamide Gel Electrophoresis

    CDK4 complex formation and kinase assays of K5-Myc epidermis. (A) Complex formation between cyclin D1 and CDK4. Fresh epidermal proteins from K5-Myc and wild-type mice were immunoprecipitated (IP) with a polyclonal antibody against cyclin D1 and immunoblotted with polyclonal antibodies against CDK4 and cyclin D1. Lanes A and B, protein lysates from K5-Myc and wild-type epidermis, respectively. (B) Kinase activity of CDK4 from K5-Myc transgenic and wild-type siblings. Fresh epidermal proteins from two transgenic and two wild-type mice were immunoprecipitated with an anti-CDK4 (IP CDK4) antibody, and in vitro kinase assays were carried out with a pRb peptide as a substrate. (C) Kinase activity of CDK2 from K5-Myc/CDK4+/+, K5-Myc/CDK4+/−, K5-Myc/CDK4−/−, and normal siblings. Fresh epidermal proteins were immunoprecipitated with an anti-CDK2 (IP CDK2) antibody and normal rabbit immunoglobulin G (NR), and in vitro kinase assays were carried out with histone H1 as a substrate.

    Journal:

    Article Title: Lack of Cyclin-Dependent Kinase 4 Inhibits c- myc Tumorigenic Activities in Epithelial Tissues

    doi: 10.1128/MCB.24.17.7538-7547.2004

    Figure Lengend Snippet: CDK4 complex formation and kinase assays of K5-Myc epidermis. (A) Complex formation between cyclin D1 and CDK4. Fresh epidermal proteins from K5-Myc and wild-type mice were immunoprecipitated (IP) with a polyclonal antibody against cyclin D1 and immunoblotted with polyclonal antibodies against CDK4 and cyclin D1. Lanes A and B, protein lysates from K5-Myc and wild-type epidermis, respectively. (B) Kinase activity of CDK4 from K5-Myc transgenic and wild-type siblings. Fresh epidermal proteins from two transgenic and two wild-type mice were immunoprecipitated with an anti-CDK4 (IP CDK4) antibody, and in vitro kinase assays were carried out with a pRb peptide as a substrate. (C) Kinase activity of CDK2 from K5-Myc/CDK4+/+, K5-Myc/CDK4+/−, K5-Myc/CDK4−/−, and normal siblings. Fresh epidermal proteins were immunoprecipitated with an anti-CDK2 (IP CDK2) antibody and normal rabbit immunoglobulin G (NR), and in vitro kinase assays were carried out with histone H1 as a substrate.

    Article Snippet: The following antibodies were used: rabbit polyclonal antibodies against CDK4 (C22), CDK2 (M2), and CDK6 (C21) (all from Santa Cruz Biotechnology, Inc., Santa Cruz, Calif.); rabbit polyclonal antibody against cyclin D1 (Ab-3) (Lab Vision Corp./Neo Markers, Fremont, Calif.); and horseradish peroxidase-conjugated secondary antibody (Amersham Corp., Arlington Heights, Ill.).

    Techniques: Immunoprecipitation, Activity Assay, Transgenic Assay, In Vitro