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primary antibodies against ccna2  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc primary antibodies against ccna2
    Information on 20 core targets.
    Primary Antibodies Against Ccna2, 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/primary antibodies against ccna2/product/Cell Signaling Technology Inc
    Average 90 stars, based on 1 article reviews
    primary antibodies against ccna2 - by Bioz Stars, 2026-03
    90/100 stars

    Images

    1) Product Images from "Anticancer Action of Xiaoxianxiong Tang in Non-Small Cell Lung Cancer by Pharmacological Analysis and Experimental Validation"

    Article Title: Anticancer Action of Xiaoxianxiong Tang in Non-Small Cell Lung Cancer by Pharmacological Analysis and Experimental Validation

    Journal: Evidence-based Complementary and Alternative Medicine : eCAM

    doi: 10.1155/2021/9930082

    Information on 20 core targets.
    Figure Legend Snippet: Information on 20 core targets.

    Techniques Used:

    The cytotoxic effects of XXXT on lung cancer cells, RT-qPCR array, and western blot for core targets. (a) The inhibition rates of H460 and A549 cells treated with XXXT (0–1000 μ g/mL) for 72 h were determined using CCK8 assay. A549 or H460 treated with XXXT at IC 50 for 72 h were harvested for analysis (b–e). (b) Heatmap of 20 core targets mRNA expression in the control group and XXXT treatment group. The significant difference of core targets in A549 and H460 cells (c) was observed, including expression of CCNA2 and FOSL2 mRNA. The protein levels of CCNA2 and FOSL2 were determined by western blot (d). Statistical analysis of CCNA2 and FOSL2 proteins expression intensity (e). The above data are presented as mean ± SD for three independent experiments. NS, not significant, ∗ P < 0.05 and ∗∗ P < 0.01 showed significant difference vs. the control group.
    Figure Legend Snippet: The cytotoxic effects of XXXT on lung cancer cells, RT-qPCR array, and western blot for core targets. (a) The inhibition rates of H460 and A549 cells treated with XXXT (0–1000 μ g/mL) for 72 h were determined using CCK8 assay. A549 or H460 treated with XXXT at IC 50 for 72 h were harvested for analysis (b–e). (b) Heatmap of 20 core targets mRNA expression in the control group and XXXT treatment group. The significant difference of core targets in A549 and H460 cells (c) was observed, including expression of CCNA2 and FOSL2 mRNA. The protein levels of CCNA2 and FOSL2 were determined by western blot (d). Statistical analysis of CCNA2 and FOSL2 proteins expression intensity (e). The above data are presented as mean ± SD for three independent experiments. NS, not significant, ∗ P < 0.05 and ∗∗ P < 0.01 showed significant difference vs. the control group.

    Techniques Used: Quantitative RT-PCR, Western Blot, Inhibition, CCK-8 Assay, Expressing, Control



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    Image Search Results


    Information on 20 core targets.

    Journal: Evidence-based Complementary and Alternative Medicine : eCAM

    Article Title: Anticancer Action of Xiaoxianxiong Tang in Non-Small Cell Lung Cancer by Pharmacological Analysis and Experimental Validation

    doi: 10.1155/2021/9930082

    Figure Lengend Snippet: Information on 20 core targets.

    Article Snippet: Primary antibodies against FOSL2 (cat. #: 15832-1-AP), α -tubulin (cat. #: 11224-1-AP), and GAPDH (cat. #: 10494-1-AP) were from Proteintech, and CCNA2 (cat. #: 4656) was from Cell Signaling Technology.

    Techniques:

    The cytotoxic effects of XXXT on lung cancer cells, RT-qPCR array, and western blot for core targets. (a) The inhibition rates of H460 and A549 cells treated with XXXT (0–1000 μ g/mL) for 72 h were determined using CCK8 assay. A549 or H460 treated with XXXT at IC 50 for 72 h were harvested for analysis (b–e). (b) Heatmap of 20 core targets mRNA expression in the control group and XXXT treatment group. The significant difference of core targets in A549 and H460 cells (c) was observed, including expression of CCNA2 and FOSL2 mRNA. The protein levels of CCNA2 and FOSL2 were determined by western blot (d). Statistical analysis of CCNA2 and FOSL2 proteins expression intensity (e). The above data are presented as mean ± SD for three independent experiments. NS, not significant, ∗ P < 0.05 and ∗∗ P < 0.01 showed significant difference vs. the control group.

    Journal: Evidence-based Complementary and Alternative Medicine : eCAM

    Article Title: Anticancer Action of Xiaoxianxiong Tang in Non-Small Cell Lung Cancer by Pharmacological Analysis and Experimental Validation

    doi: 10.1155/2021/9930082

    Figure Lengend Snippet: The cytotoxic effects of XXXT on lung cancer cells, RT-qPCR array, and western blot for core targets. (a) The inhibition rates of H460 and A549 cells treated with XXXT (0–1000 μ g/mL) for 72 h were determined using CCK8 assay. A549 or H460 treated with XXXT at IC 50 for 72 h were harvested for analysis (b–e). (b) Heatmap of 20 core targets mRNA expression in the control group and XXXT treatment group. The significant difference of core targets in A549 and H460 cells (c) was observed, including expression of CCNA2 and FOSL2 mRNA. The protein levels of CCNA2 and FOSL2 were determined by western blot (d). Statistical analysis of CCNA2 and FOSL2 proteins expression intensity (e). The above data are presented as mean ± SD for three independent experiments. NS, not significant, ∗ P < 0.05 and ∗∗ P < 0.01 showed significant difference vs. the control group.

    Article Snippet: Primary antibodies against FOSL2 (cat. #: 15832-1-AP), α -tubulin (cat. #: 11224-1-AP), and GAPDH (cat. #: 10494-1-AP) were from Proteintech, and CCNA2 (cat. #: 4656) was from Cell Signaling Technology.

    Techniques: Quantitative RT-PCR, Western Blot, Inhibition, CCK-8 Assay, Expressing, Control