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pc3 whole cell lysates  (Santa Cruz Biotechnology)


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    Santa Cruz Biotechnology pc3 whole cell lysates
    Pc3 Whole Cell Lysates, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 69 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pc3+whole+cell+lysates/PC-3+Cell+Lysate/pm23468933-140-4-12
    Average 93 stars, based on 69 article reviews
    pc3 whole cell lysates - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Immunoprecipitation:

    Article Title: Cysteine (C)-X-C Receptor 4 Undergoes Transportin 1-Dependent Nuclear Localization and Remains Functional at the Nucleus of Metastatic Prostate Cancer Cells
    Article Snippet: Expression of TRN1 was detected with a mouse monoclonal antibody (Santa Cruz; 1∶1000); α-Tubulin or β-Actin was used as a loading control. .. One milligram of PC3 whole cell lysates were immunoprecipitated for CXCR4 (Santa Cruz; 1 μg per 250 μg of protein) overnight at 4°C, followed by incubation with Protein A/G Plus-Agarose beads (Santa Cruz) for 2 hrs at 4°C. ..

    Article Title: Cysteine (C)-x-C receptor 4 undergoes transportin 1-dependent nuclear localization and remains functional at the nucleus of metastatic prostate cancer cells.
    Article Snippet: Expression of TRN1 was detected with a mouse monoclonal antibody (Santa Cruz; 1:1000); a-Tubulin or b-Actin was used as a loading control. .. Immunoprecipitation One milligram of PC3 whole cell lysates were immunoprecipitated for CXCR4 (Santa Cruz; 1 mg per 250 mg of protein) overnight at 4uC, followed by incubation with Protein A/G PlusAgarose beads (Santa Cruz) for 2 hrs at 4uC. ..

    Incubation:

    Article Title: Cysteine (C)-X-C Receptor 4 Undergoes Transportin 1-Dependent Nuclear Localization and Remains Functional at the Nucleus of Metastatic Prostate Cancer Cells
    Article Snippet: Expression of TRN1 was detected with a mouse monoclonal antibody (Santa Cruz; 1∶1000); α-Tubulin or β-Actin was used as a loading control. .. One milligram of PC3 whole cell lysates were immunoprecipitated for CXCR4 (Santa Cruz; 1 μg per 250 μg of protein) overnight at 4°C, followed by incubation with Protein A/G Plus-Agarose beads (Santa Cruz) for 2 hrs at 4°C. ..

    Article Title: Cysteine (C)-x-C receptor 4 undergoes transportin 1-dependent nuclear localization and remains functional at the nucleus of metastatic prostate cancer cells.
    Article Snippet: Expression of TRN1 was detected with a mouse monoclonal antibody (Santa Cruz; 1:1000); a-Tubulin or b-Actin was used as a loading control. .. Immunoprecipitation One milligram of PC3 whole cell lysates were immunoprecipitated for CXCR4 (Santa Cruz; 1 mg per 250 mg of protein) overnight at 4uC, followed by incubation with Protein A/G PlusAgarose beads (Santa Cruz) for 2 hrs at 4uC. ..



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    P16INK4A subcellular localization by immunofluorescence in HeLa cells using anti-p16INK4a antibodies F-12 ( A ), H-156 ( B ), JC8 ( C ), and E6H4 ( D ); magnification bar = 20 µm. E . Comparison of anti-p16INK4a antibodies in Western Blot analysis using p16INK4a positive Hek293 and HeLa whole cell lysates and p16INK4a negative <t>PC3</t> cell extract (each loaded 20 µg whole protein per well). F . Immunoprecipitation of p16INK4a using F-12 and JC8 mouse monoclonal antibodies, the FLAG mouse monoclonal antibody was used alongside as a negative control.
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    P16INK4A subcellular localization by immunofluorescence in HeLa cells using anti-p16INK4a antibodies F-12 ( A ), H-156 ( B ), JC8 ( C ), and E6H4 ( D ); magnification bar = 20 µm. E . Comparison of anti-p16INK4a antibodies in Western Blot analysis using p16INK4a positive Hek293 and HeLa whole cell lysates and p16INK4a negative <t>PC3</t> cell extract (each loaded 20 µg whole protein per well). F . Immunoprecipitation of p16INK4a using F-12 and JC8 mouse monoclonal antibodies, the FLAG mouse monoclonal antibody was used alongside as a negative control.
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    P16INK4A subcellular localization by immunofluorescence in HeLa cells using anti-p16INK4a antibodies F-12 ( A ), H-156 ( B ), JC8 ( C ), and E6H4 ( D ); magnification bar = 20 µm. E . Comparison of anti-p16INK4a antibodies in Western Blot analysis using p16INK4a positive Hek293 and HeLa whole cell lysates and p16INK4a negative PC3 cell extract (each loaded 20 µg whole protein per well). F . Immunoprecipitation of p16INK4a using F-12 and JC8 mouse monoclonal antibodies, the FLAG mouse monoclonal antibody was used alongside as a negative control.

    Journal: PLoS ONE

    Article Title: The Specificity and Patterns of Staining in Human Cells and Tissues of p16INK4a Antibodies Demonstrate Variant Antigen Binding

    doi: 10.1371/journal.pone.0053313

    Figure Lengend Snippet: P16INK4A subcellular localization by immunofluorescence in HeLa cells using anti-p16INK4a antibodies F-12 ( A ), H-156 ( B ), JC8 ( C ), and E6H4 ( D ); magnification bar = 20 µm. E . Comparison of anti-p16INK4a antibodies in Western Blot analysis using p16INK4a positive Hek293 and HeLa whole cell lysates and p16INK4a negative PC3 cell extract (each loaded 20 µg whole protein per well). F . Immunoprecipitation of p16INK4a using F-12 and JC8 mouse monoclonal antibodies, the FLAG mouse monoclonal antibody was used alongside as a negative control.

    Article Snippet: PC3 whole cell lysate was purchased from Santa Cruz Biotechnology.

    Techniques: Immunofluorescence, Comparison, Western Blot, Immunoprecipitation, Bioprocessing, Negative Control