rabbit anti cdk2 antibody Search Results


90
Boster Bio rabbit anti cdk2
Rabbit Anti Cdk2, 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/rabbit anti cdk2/product/Boster Bio
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rabbit anti cdk2 - by Bioz Stars, 2026-02
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Signalway Antibody rabbit anti-cdk2
Intracellular localization of FAM129B in exponential and confluent cell cultures. A, HeLa cells (5 × 106) were harvested during the late exponential growth phase, and the cell extracts were fractionated into cytoplasmic (Cyt) and nuclear (Nuc) fractions (as described under “Experimental Procedures”). The fractions were analyzed by immunoblotting using antibodies directed against FAM129B, PARP, p53, CDK6, and <t>CDK2.</t> B, the same procedure was used to analyze NIH3T3 cell fractions. C, immunofluorescence microscopy of exponentially growing HeLa cells stained with a Hoechst 33342 DNA stain and with antibodies directed against rabbit FAM129B and the secondary antibody, chicken anti-rabbit IgG Alexa Fluor 594. The same protocol was followed for the cells in confluent HeLa cells (D) and an exponentially growing HeLa culture showing some mitotic cells (E). F, immunofluorescence co-localization (as described under “Experimental Procedures”) of FAM129B and β-catenin. The confluent cells were co-stained with rabbit antibodies directed against FAM129B and mouse antibodies directed against β-catenin. The secondary antibodies were Alexa Fluor 594-conjugated anti-rabbit IgG and an Alexa Fluor 488-conjugated anti-mouse IgG antibody. The cells were also stained with Hoechst 33342.
Rabbit Anti Cdk2, supplied by Signalway Antibody, 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 anti-cdk2/product/Signalway Antibody
Average 90 stars, based on 1 article reviews
rabbit anti-cdk2 - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier

90
Covance rabbit anti-cdk-2 polyclonal antibody
Intracellular localization of FAM129B in exponential and confluent cell cultures. A, HeLa cells (5 × 106) were harvested during the late exponential growth phase, and the cell extracts were fractionated into cytoplasmic (Cyt) and nuclear (Nuc) fractions (as described under “Experimental Procedures”). The fractions were analyzed by immunoblotting using antibodies directed against FAM129B, PARP, p53, CDK6, and <t>CDK2.</t> B, the same procedure was used to analyze NIH3T3 cell fractions. C, immunofluorescence microscopy of exponentially growing HeLa cells stained with a Hoechst 33342 DNA stain and with antibodies directed against rabbit FAM129B and the secondary antibody, chicken anti-rabbit IgG Alexa Fluor 594. The same protocol was followed for the cells in confluent HeLa cells (D) and an exponentially growing HeLa culture showing some mitotic cells (E). F, immunofluorescence co-localization (as described under “Experimental Procedures”) of FAM129B and β-catenin. The confluent cells were co-stained with rabbit antibodies directed against FAM129B and mouse antibodies directed against β-catenin. The secondary antibodies were Alexa Fluor 594-conjugated anti-rabbit IgG and an Alexa Fluor 488-conjugated anti-mouse IgG antibody. The cells were also stained with Hoechst 33342.
Rabbit Anti Cdk 2 Polyclonal Antibody, supplied by Covance, 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 anti-cdk-2 polyclonal antibody/product/Covance
Average 90 stars, based on 1 article reviews
rabbit anti-cdk-2 polyclonal antibody - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier

Image Search Results


Intracellular localization of FAM129B in exponential and confluent cell cultures. A, HeLa cells (5 × 106) were harvested during the late exponential growth phase, and the cell extracts were fractionated into cytoplasmic (Cyt) and nuclear (Nuc) fractions (as described under “Experimental Procedures”). The fractions were analyzed by immunoblotting using antibodies directed against FAM129B, PARP, p53, CDK6, and CDK2. B, the same procedure was used to analyze NIH3T3 cell fractions. C, immunofluorescence microscopy of exponentially growing HeLa cells stained with a Hoechst 33342 DNA stain and with antibodies directed against rabbit FAM129B and the secondary antibody, chicken anti-rabbit IgG Alexa Fluor 594. The same protocol was followed for the cells in confluent HeLa cells (D) and an exponentially growing HeLa culture showing some mitotic cells (E). F, immunofluorescence co-localization (as described under “Experimental Procedures”) of FAM129B and β-catenin. The confluent cells were co-stained with rabbit antibodies directed against FAM129B and mouse antibodies directed against β-catenin. The secondary antibodies were Alexa Fluor 594-conjugated anti-rabbit IgG and an Alexa Fluor 488-conjugated anti-mouse IgG antibody. The cells were also stained with Hoechst 33342.

Journal: The Journal of Biological Chemistry

Article Title: FAM129B/MINERVA, a Novel Adherens Junction-associated Protein, Suppresses Apoptosis in HeLa Cells *

doi: 10.1074/jbc.M110.175273

Figure Lengend Snippet: Intracellular localization of FAM129B in exponential and confluent cell cultures. A, HeLa cells (5 × 106) were harvested during the late exponential growth phase, and the cell extracts were fractionated into cytoplasmic (Cyt) and nuclear (Nuc) fractions (as described under “Experimental Procedures”). The fractions were analyzed by immunoblotting using antibodies directed against FAM129B, PARP, p53, CDK6, and CDK2. B, the same procedure was used to analyze NIH3T3 cell fractions. C, immunofluorescence microscopy of exponentially growing HeLa cells stained with a Hoechst 33342 DNA stain and with antibodies directed against rabbit FAM129B and the secondary antibody, chicken anti-rabbit IgG Alexa Fluor 594. The same protocol was followed for the cells in confluent HeLa cells (D) and an exponentially growing HeLa culture showing some mitotic cells (E). F, immunofluorescence co-localization (as described under “Experimental Procedures”) of FAM129B and β-catenin. The confluent cells were co-stained with rabbit antibodies directed against FAM129B and mouse antibodies directed against β-catenin. The secondary antibodies were Alexa Fluor 594-conjugated anti-rabbit IgG and an Alexa Fluor 488-conjugated anti-mouse IgG antibody. The cells were also stained with Hoechst 33342.

Article Snippet: Antibodies and Reagents Antibodies used for this study were rabbit anti-FAM129B (catalog no. 5122), rabbit anti-caspase-3 (catalog no. 9662), rabbit anti-cleaved caspase-3 (catalog no. 9664), rabbit anti-poly(ADP-ribose) polymerase (PARP 3 ; catalog no. 9542), rabbit anti-caspase-9 antibody (catalog no. 9502), mouse monoclonal anti-cdk6 (catalog no. 3136), mouse anti-caspase-8 (catalog no. 9746) (Cell Signaling, Beverly, MA); rabbit anti-cdk2 (catalog no. 21111) and rabbit anti-Akt (catalog no. 21054) (Signalway Antibody, Pearland, TX), mouse monoclonal antibody anti-β-catenin (catalog no. 610154) (BD Transduction Laboratories), mouse monoclonal anti-p53 (catalog no. sc-126), mouse monoclonal anti-GFP (catalog no. sc-9996), and mouse monoclonal β-tubulin (catalog no. sc-5274) (Santa Cruz Biotechnology, Inc., Santa Cruz).

Techniques: Western Blot, Immunofluorescence, Microscopy, Staining