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rabbit polyclonal anti cdk6 antibody  (Proteintech)


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    Proteintech rabbit polyclonal anti cdk6 antibody
    Rabbit Polyclonal Anti Cdk6 Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 313 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+polyclonal+anti+cdk6+antibody/CDK6+Antibody/pm40471359-43-1-6
    Average 96 stars, based on 313 article reviews
    rabbit polyclonal anti cdk6 antibody - by Bioz Stars, 2026-10
    96/100 stars

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    Proteintech rabbit polyclonal anti cdk6 antibody
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    Bethyl rabbit polyclonal anti cdk6 antibody
    (A) Scatter plot of EBV-mediated effects on primary human B cell gene expression Y axis, Log2 (LCL to primary B-cell ratios); X axis, −log10 (p-value). Values (Price et al., 2012) of top LCL-selective hits (red circle) versus all other B cell genes (blue circle) are shown. (B) Ratios of EBV-induced to EBV-suppressed primary B-cell host genes for genome-wide (gray bar) versus for the 87 LCL-selective screen hits at q <0.05 cutoff (black bar). (C) CRISPR screens identified distinct GM12878 and P3HR1 cyclin/cyclin-dependent kinase dependencies. Data are expressed as Log2 normalized values of sgRNA abundance from quadruplicate screens. The four sgRNAs against CDK4 (triangle), CCND3 (square), <t>CDK6</t> (closed circle) and CCND2 (diamond) are highlighted among all Avana sgRNA library abundances (open circle). (D) Immunoblot analysis of CDK4 or CDK6 knockout in whole cell extracts of GM12878 or P3HR1 with the indicated sgRNAs. (E-F) Growth curves of GM12878 versus P3HR1 Cas9 cells expressing CDK6 (red), CDK4 (blue) or non-targeting control (black) sgRNA. Mean and standard deviation (S.D.) of triplicate experiments are shown. See also Figure S1.
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    (A) Scatter plot of EBV-mediated effects on primary human B cell gene expression Y axis, Log2 (LCL to primary B-cell ratios); X axis, −log10 (p-value). Values (Price et al., 2012) of top LCL-selective hits (red circle) versus all other B cell genes (blue circle) are shown. (B) Ratios of EBV-induced to EBV-suppressed primary B-cell host genes for genome-wide (gray bar) versus for the 87 LCL-selective screen hits at q <0.05 cutoff (black bar). (C) CRISPR screens identified distinct GM12878 and P3HR1 cyclin/cyclin-dependent kinase dependencies. Data are expressed as Log2 normalized values of sgRNA abundance from quadruplicate screens. The four sgRNAs against CDK4 (triangle), CCND3 (square), <t>CDK6</t> (closed circle) and CCND2 (diamond) are highlighted among all Avana sgRNA library abundances (open circle). (D) Immunoblot analysis of CDK4 or CDK6 knockout in whole cell extracts of GM12878 or P3HR1 with the indicated sgRNAs. (E-F) Growth curves of GM12878 versus P3HR1 Cas9 cells expressing CDK6 (red), CDK4 (blue) or non-targeting control (black) sgRNA. Mean and standard deviation (S.D.) of triplicate experiments are shown. See also Figure S1.
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    (A) Scatter plot of EBV-mediated effects on primary human B cell gene expression Y axis, Log2 (LCL to primary B-cell ratios); X axis, −log10 (p-value). Values (Price et al., 2012) of top LCL-selective hits (red circle) versus all other B cell genes (blue circle) are shown. (B) Ratios of EBV-induced to EBV-suppressed primary B-cell host genes for genome-wide (gray bar) versus for the 87 LCL-selective screen hits at q <0.05 cutoff (black bar). (C) CRISPR screens identified distinct GM12878 and P3HR1 cyclin/cyclin-dependent kinase dependencies. Data are expressed as Log2 normalized values of sgRNA abundance from quadruplicate screens. The four sgRNAs against CDK4 (triangle), CCND3 (square), <t>CDK6</t> (closed circle) and CCND2 (diamond) are highlighted among all Avana sgRNA library abundances (open circle). (D) Immunoblot analysis of CDK4 or CDK6 knockout in whole cell extracts of GM12878 or P3HR1 with the indicated sgRNAs. (E-F) Growth curves of GM12878 versus P3HR1 Cas9 cells expressing CDK6 (red), CDK4 (blue) or non-targeting control (black) sgRNA. Mean and standard deviation (S.D.) of triplicate experiments are shown. See also Figure S1.
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    Sangon Biotech anti-cdk6 rabbit polyclonal antibody
    Information of primers for real-time quantitative PCR.
    Anti Cdk6 Rabbit Polyclonal Antibody, supplied by Sangon Biotech, 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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    Image Search Results


    Journal: iScience

    Article Title: Cdk6’s functions are critically regulated by its unique C-terminus

    doi: 10.1016/j.isci.2024.111697

    Figure Lengend Snippet:

    Article Snippet: Rabbit polyclonal anti-CDK6 , Santa Cruz Biotechnology , Cat# sc-7180; RRID: AB_2076998.

    Techniques: Recombinant, Luciferase, Magnetic Beads, Immunoprecipitation, Bicinchoninic Acid Protein Assay, Mass Spectrometry, Modification, cDNA Synthesis, SYBR Green Assay, Western Blot, Bradford Protein Assay, Software

    KEY RESOURCES TABLE

    Journal: Molecular cell

    Article Title: Phosphorylated RB Promotes Cancer Immunity by Inhibiting NF-κB Activation and PD-L1 Expression

    doi: 10.1016/j.molcel.2018.10.034

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Rabbit polyclonal anti-CDK6 , Santa Cruz , Cat# sc-177; RRID: AB_631225.

    Techniques: Virus, Recombinant, Control, Mutagenesis, Kinase Assay, Sequencing, CRAfT Assay, Software

    (A) Scatter plot of EBV-mediated effects on primary human B cell gene expression Y axis, Log2 (LCL to primary B-cell ratios); X axis, −log10 (p-value). Values (Price et al., 2012) of top LCL-selective hits (red circle) versus all other B cell genes (blue circle) are shown. (B) Ratios of EBV-induced to EBV-suppressed primary B-cell host genes for genome-wide (gray bar) versus for the 87 LCL-selective screen hits at q <0.05 cutoff (black bar). (C) CRISPR screens identified distinct GM12878 and P3HR1 cyclin/cyclin-dependent kinase dependencies. Data are expressed as Log2 normalized values of sgRNA abundance from quadruplicate screens. The four sgRNAs against CDK4 (triangle), CCND3 (square), CDK6 (closed circle) and CCND2 (diamond) are highlighted among all Avana sgRNA library abundances (open circle). (D) Immunoblot analysis of CDK4 or CDK6 knockout in whole cell extracts of GM12878 or P3HR1 with the indicated sgRNAs. (E-F) Growth curves of GM12878 versus P3HR1 Cas9 cells expressing CDK6 (red), CDK4 (blue) or non-targeting control (black) sgRNA. Mean and standard deviation (S.D.) of triplicate experiments are shown. See also Figure S1.

    Journal: Cell host & microbe

    Article Title: CRISPR/Cas9 Screens Reveal Epstein-Barr Virus Transformed B-Cell Host Dependency Factors

    doi: 10.1016/j.chom.2017.04.005

    Figure Lengend Snippet: (A) Scatter plot of EBV-mediated effects on primary human B cell gene expression Y axis, Log2 (LCL to primary B-cell ratios); X axis, −log10 (p-value). Values (Price et al., 2012) of top LCL-selective hits (red circle) versus all other B cell genes (blue circle) are shown. (B) Ratios of EBV-induced to EBV-suppressed primary B-cell host genes for genome-wide (gray bar) versus for the 87 LCL-selective screen hits at q <0.05 cutoff (black bar). (C) CRISPR screens identified distinct GM12878 and P3HR1 cyclin/cyclin-dependent kinase dependencies. Data are expressed as Log2 normalized values of sgRNA abundance from quadruplicate screens. The four sgRNAs against CDK4 (triangle), CCND3 (square), CDK6 (closed circle) and CCND2 (diamond) are highlighted among all Avana sgRNA library abundances (open circle). (D) Immunoblot analysis of CDK4 or CDK6 knockout in whole cell extracts of GM12878 or P3HR1 with the indicated sgRNAs. (E-F) Growth curves of GM12878 versus P3HR1 Cas9 cells expressing CDK6 (red), CDK4 (blue) or non-targeting control (black) sgRNA. Mean and standard deviation (S.D.) of triplicate experiments are shown. See also Figure S1.

    Article Snippet: Rabbit polyclonal anti-CDK6 antibody , Bethyl , Cat#A304-937A; RRID: AB_2621131.

    Techniques: Gene Expression, Genome Wide, CRISPR, Western Blot, Knock-Out, Expressing, Control, Standard Deviation

    KEY RESOURCES TABLE

    Journal: Cell host & microbe

    Article Title: CRISPR/Cas9 Screens Reveal Epstein-Barr Virus Transformed B-Cell Host Dependency Factors

    doi: 10.1016/j.chom.2017.04.005

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Rabbit polyclonal anti-CDK6 antibody , Bethyl , Cat#A304-937A; RRID: AB_2621131.

    Techniques: Purification, Virus, Recombinant, SYBR Green Assay, Cell Viability Assay, Caspase-Glo Assay, Isolation, Cell Culture, Control, CRISPR, Software

    Information of primers for real-time quantitative PCR.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Roles of Melatonin in Goat Hair Follicle Stem Cell Proliferation and Pluripotency Through Regulating the Wnt Signaling Pathway

    doi: 10.3389/fcell.2021.686805

    Figure Lengend Snippet: Information of primers for real-time quantitative PCR.

    Article Snippet: Cyclin-dependent kinase 6 , Anti-CDK6 rabbit polyclonal antibody , Sangon Biotech , D120398.

    Techniques: Binding Assay

    List of antibodies used for Immunofluorescence analysis and western blot.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Roles of Melatonin in Goat Hair Follicle Stem Cell Proliferation and Pluripotency Through Regulating the Wnt Signaling Pathway

    doi: 10.3389/fcell.2021.686805

    Figure Lengend Snippet: List of antibodies used for Immunofluorescence analysis and western blot.

    Article Snippet: Cyclin-dependent kinase 6 , Anti-CDK6 rabbit polyclonal antibody , Sangon Biotech , D120398.

    Techniques: Immunofluorescence, Western Blot, Binding Assay, Recombinant

    Melatonin promoted the proliferation and cell cycle of gsHFSCs by promoting Wnt downstream factor expression, ∗∗∗ p < 0.001. (A) MTT analysis of melatonin on gsHFSCs proliferation following 72 h of exposure. (B) Cell cycle analysis of gsHFSCs after melatonin exposure at 72 h. (C) Relative mRNA level of C-JUN , C-MYC, CYCLIND1 , and CDK6 as detected by RT-qPCR after melatonin exposure for 72 h; ∗∗ p < 0.01, ∗ p < 0.05 (Control: green; 72 h melatonin: blue). (D) Proteins tested by immunofluorescence staining. Scale bar, 50 μm.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Roles of Melatonin in Goat Hair Follicle Stem Cell Proliferation and Pluripotency Through Regulating the Wnt Signaling Pathway

    doi: 10.3389/fcell.2021.686805

    Figure Lengend Snippet: Melatonin promoted the proliferation and cell cycle of gsHFSCs by promoting Wnt downstream factor expression, ∗∗∗ p < 0.001. (A) MTT analysis of melatonin on gsHFSCs proliferation following 72 h of exposure. (B) Cell cycle analysis of gsHFSCs after melatonin exposure at 72 h. (C) Relative mRNA level of C-JUN , C-MYC, CYCLIND1 , and CDK6 as detected by RT-qPCR after melatonin exposure for 72 h; ∗∗ p < 0.01, ∗ p < 0.05 (Control: green; 72 h melatonin: blue). (D) Proteins tested by immunofluorescence staining. Scale bar, 50 μm.

    Article Snippet: Cyclin-dependent kinase 6 , Anti-CDK6 rabbit polyclonal antibody , Sangon Biotech , D120398.

    Techniques: Expressing, Cell Cycle Assay, Quantitative RT-PCR, Control, Immunofluorescence, Staining