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rabbit anti cyclin e antibody  (Bethyl)


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    Structured Review

    Bethyl rabbit anti cyclin e antibody
    Rabbit Anti Cyclin E Antibody, supplied by Bethyl, used in various techniques. Bioz Stars score: 91/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+cyclin+e+antibody/Cyclin+Y+Antibody/pmc12091888-214-91-96
    Average 91 stars, based on 3 article reviews
    rabbit anti cyclin e antibody - by Bioz Stars, 2026-09
    91/100 stars

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    Related Articles

    Immunostaining:

    Article Title: STAT3, MYC, and EBNA1 cooperate through a ZC3H18 transcriptional network to regulate survival and proliferation of EBV-positive lymphomas
    Article Snippet: .. The following antibodies were used for immunostaining: rabbit anti-STAT3 antibody (4904S, Cell Signaling Technology), mouse anti-EBNA1 antibody (sc-81581, Santa Cruz Biotechnology), rabbit anti-MYC antibody (A190-105A, Bethyl Laboratories), mouse anti-β-actin antibody (clone AC-15) (A1978, Sigma-Aldrich), rabbit anti-phospho-IκBα (Ser32) antibody (2859S, Cell Signaling Technology), rabbit anti-IκBα antibody (9242S, Cell Signaling Technology), rabbit anti-p65 antibody (8242S, Cell Signaling Technology), rabbit anti-p50 antibody (13586, Cell Signaling Technology), rabbit anti-ZC3H18 antibody (A304-682A, Bethyl Laboratories), rabbit anti-Caspase 3 antibody (GTX110543, GeneTex), mouse anti-Cyclin A antibody (sc-53228, Santa Cruz Biotechnology), rabbit anti-Cyclin B antibody (4138S, Cell Signaling Technology), rabbit anti-Cyclin E antibody (A301-566, Bethyl Laboratories), mouse anti-ZEBRA antibody (sc-53904, Santa Cruz Biotechnology), rabbit anti-PCNA antibody (A300-276, Bethyl Laboratories), HRP-conjugated goat anti-mouse IgG (626520, Thermo Fisher Scientific), and HRP-conjugated goat anti-rabbit IgG (31460, Thermo Fisher Scientific). ..



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    6-Gingerol regulates cell cycle-related proteins in THP-1 cells under high-glucose conditions. ( A ) Western blot analysis of CDK4, Cyclin D1, and <t>Cyclin</t> <t>E</t> protein expression in THP-1 cells treated with glucose (0, 5.5 or 25 mM) and 6-gingerol (30 or 60 µM) for 24 h. Protein levels were normalized to β-actin and quantified by densitometry. ( B ) Quantitative real-time PCR (qPCR) analysis of CDK4 , CCND1 , and CCNE1 mRNA expression under the same treatment conditions. mRNA levels were normalized to GAPDH and expressed relative to the untreated control. ( C ) Western blot analysis of p21, p27, p53, MDM2, and phosphorylated MDM2 (p-MDM2) protein expression following 24 h of treatment. ( D ) qPCR analysis of CDKN1A , CDKN1B , and TP53 mRNA expression, normalized to GAPDH and expressed relative to control. All data represent the mean ± SEM from three independent experiments. Statistical significance was assessed by one-way ANOVA. # p < 0.001 versus control; *** p < 0.001.
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    Santa Cruz Biotechnology ib fig s2a ib fig s2c rabbit polyclonal anti cyclin e sc 481 m 20
    6-Gingerol regulates cell cycle-related proteins in THP-1 cells under high-glucose conditions. ( A ) Western blot analysis of CDK4, Cyclin D1, and <t>Cyclin</t> <t>E</t> protein expression in THP-1 cells treated with glucose (0, 5.5 or 25 mM) and 6-gingerol (30 or 60 µM) for 24 h. Protein levels were normalized to β-actin and quantified by densitometry. ( B ) Quantitative real-time PCR (qPCR) analysis of CDK4 , CCND1 , and CCNE1 mRNA expression under the same treatment conditions. mRNA levels were normalized to GAPDH and expressed relative to the untreated control. ( C ) Western blot analysis of p21, p27, p53, MDM2, and phosphorylated MDM2 (p-MDM2) protein expression following 24 h of treatment. ( D ) qPCR analysis of CDKN1A , CDKN1B , and TP53 mRNA expression, normalized to GAPDH and expressed relative to control. All data represent the mean ± SEM from three independent experiments. Statistical significance was assessed by one-way ANOVA. # p < 0.001 versus control; *** p < 0.001.
    Ib Fig S2a Ib Fig S2c Rabbit Polyclonal Anti Cyclin E Sc 481 M 20, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    6-Gingerol regulates cell cycle-related proteins in THP-1 cells under high-glucose conditions. ( A ) Western blot analysis of CDK4, Cyclin D1, and Cyclin E protein expression in THP-1 cells treated with glucose (0, 5.5 or 25 mM) and 6-gingerol (30 or 60 µM) for 24 h. Protein levels were normalized to β-actin and quantified by densitometry. ( B ) Quantitative real-time PCR (qPCR) analysis of CDK4 , CCND1 , and CCNE1 mRNA expression under the same treatment conditions. mRNA levels were normalized to GAPDH and expressed relative to the untreated control. ( C ) Western blot analysis of p21, p27, p53, MDM2, and phosphorylated MDM2 (p-MDM2) protein expression following 24 h of treatment. ( D ) qPCR analysis of CDKN1A , CDKN1B , and TP53 mRNA expression, normalized to GAPDH and expressed relative to control. All data represent the mean ± SEM from three independent experiments. Statistical significance was assessed by one-way ANOVA. # p < 0.001 versus control; *** p < 0.001.

    Journal: Scientific Reports

    Article Title: 6-Gingerol alleviates high glucose-induced inflammation and cytotoxicity in THP-1 cells by inhibiting TLR4 signaling

    doi: 10.1038/s41598-025-34192-z

    Figure Lengend Snippet: 6-Gingerol regulates cell cycle-related proteins in THP-1 cells under high-glucose conditions. ( A ) Western blot analysis of CDK4, Cyclin D1, and Cyclin E protein expression in THP-1 cells treated with glucose (0, 5.5 or 25 mM) and 6-gingerol (30 or 60 µM) for 24 h. Protein levels were normalized to β-actin and quantified by densitometry. ( B ) Quantitative real-time PCR (qPCR) analysis of CDK4 , CCND1 , and CCNE1 mRNA expression under the same treatment conditions. mRNA levels were normalized to GAPDH and expressed relative to the untreated control. ( C ) Western blot analysis of p21, p27, p53, MDM2, and phosphorylated MDM2 (p-MDM2) protein expression following 24 h of treatment. ( D ) qPCR analysis of CDKN1A , CDKN1B , and TP53 mRNA expression, normalized to GAPDH and expressed relative to control. All data represent the mean ± SEM from three independent experiments. Statistical significance was assessed by one-way ANOVA. # p < 0.001 versus control; *** p < 0.001.

    Article Snippet: Primary antibodies against TLR4 (sc-293072), p-IκBα (sc-8404), and β-actin (sc-47778), along with secondary antibodies (anti-mouse (sc-516102) and anti-rabbit (sc-2357)), COX‐1 (sc‐19998), COX‐2 (sc‐19999), cyclin E (sc-481), p21 (sc-756), and CDK4 (sc-260), were acquired from Santa Cruz Biotechnology, Inc. (Dallas, TX, USA).

    Techniques: Western Blot, Expressing, Real-time Polymerase Chain Reaction, Control