Review



rabbit polyclonal antibodies against cyp3a  (Boster Bio)


Bioz Verified Symbol Boster Bio is a verified supplier
Bioz Manufacturer Symbol Boster Bio manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 90
      Buy from Supplier

    Structured Review

    Boster Bio rabbit polyclonal antibodies against cyp3a
    Rats were treated with BCG (125 mg kg -1 , intravenously, once for 2 wks) or BCG + HRP (50, 100, or 200 mg kg -1 d -1 , oral administration for 13d). Liver proteins were extracted to determine NF-κB, iNOS, and <t>CYP3A</t> expression. Equal amounts (30 μg) of protein were subjected to SDS-PAGE followed by western blot analysis using anti-NF-κB, anti-iNOS, and anti-CYP3A antibodies. Results were normalized to LMNA or GAPDH. NF-κB (A), iNOS (B), and CYP3A (C) protein expression levels in rat liver were measured by western blot. NF-κB, iNOS, and CYP3A expression levels were quantified by ImageQuant software (GE Healthcare Life Science, Little Chalfont, UK). Data represent means ± SD of three independent experiments. Asterisks stars above bars indicate differences between groups.
    Rabbit Polyclonal Antibodies Against Cyp3a, supplied by Boster Bio, used in various techniques. Bioz Stars score: 90/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal antibodies against cyp3a/product/Boster Bio
    Average 90 stars, based on 4 article reviews
    rabbit polyclonal antibodies against cyp3a - by Bioz Stars, 2026-03
    90/100 stars

    Images

    1) Product Images from "Involvement of NF-κB in the reversal of CYP3A down-regulation induced by sea buckthorn in BCG-induced rats"

    Article Title: Involvement of NF-κB in the reversal of CYP3A down-regulation induced by sea buckthorn in BCG-induced rats

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0238810

    Rats were treated with BCG (125 mg kg -1 , intravenously, once for 2 wks) or BCG + HRP (50, 100, or 200 mg kg -1 d -1 , oral administration for 13d). Liver proteins were extracted to determine NF-κB, iNOS, and CYP3A expression. Equal amounts (30 μg) of protein were subjected to SDS-PAGE followed by western blot analysis using anti-NF-κB, anti-iNOS, and anti-CYP3A antibodies. Results were normalized to LMNA or GAPDH. NF-κB (A), iNOS (B), and CYP3A (C) protein expression levels in rat liver were measured by western blot. NF-κB, iNOS, and CYP3A expression levels were quantified by ImageQuant software (GE Healthcare Life Science, Little Chalfont, UK). Data represent means ± SD of three independent experiments. Asterisks stars above bars indicate differences between groups.
    Figure Legend Snippet: Rats were treated with BCG (125 mg kg -1 , intravenously, once for 2 wks) or BCG + HRP (50, 100, or 200 mg kg -1 d -1 , oral administration for 13d). Liver proteins were extracted to determine NF-κB, iNOS, and CYP3A expression. Equal amounts (30 μg) of protein were subjected to SDS-PAGE followed by western blot analysis using anti-NF-κB, anti-iNOS, and anti-CYP3A antibodies. Results were normalized to LMNA or GAPDH. NF-κB (A), iNOS (B), and CYP3A (C) protein expression levels in rat liver were measured by western blot. NF-κB, iNOS, and CYP3A expression levels were quantified by ImageQuant software (GE Healthcare Life Science, Little Chalfont, UK). Data represent means ± SD of three independent experiments. Asterisks stars above bars indicate differences between groups.

    Techniques Used: Expressing, SDS Page, Western Blot, Software

    Rats were treated with BCG (125 mg kg-1, intravenously, once for 2 wks) or BCG + HRP (50, 100, or 200 mg•kg -1 •d -1 , oral administration for 13d). The mRNA expression of CYP3A was measured by real-time PCR. Each bar represents the mean ± SD from three independent experiments (n = 10/group). Asterisks stars above bars indicate differences between groups. The significance of the data was determined by one-way analysis of variance (ANOVA) followed by Tukey’s test.
    Figure Legend Snippet: Rats were treated with BCG (125 mg kg-1, intravenously, once for 2 wks) or BCG + HRP (50, 100, or 200 mg•kg -1 •d -1 , oral administration for 13d). The mRNA expression of CYP3A was measured by real-time PCR. Each bar represents the mean ± SD from three independent experiments (n = 10/group). Asterisks stars above bars indicate differences between groups. The significance of the data was determined by one-way analysis of variance (ANOVA) followed by Tukey’s test.

    Techniques Used: Expressing, Real-time Polymerase Chain Reaction



    Similar Products

    rabbit polyclonal antibodies against cyp3a  (Boster Bio)
    90
    Boster Bio rabbit polyclonal antibodies against cyp3a
    Rats were treated with BCG (125 mg kg -1 , intravenously, once for 2 wks) or BCG + HRP (50, 100, or 200 mg kg -1 d -1 , oral administration for 13d). Liver proteins were extracted to determine NF-κB, iNOS, and <t>CYP3A</t> expression. Equal amounts (30 μg) of protein were subjected to SDS-PAGE followed by western blot analysis using anti-NF-κB, anti-iNOS, and anti-CYP3A antibodies. Results were normalized to LMNA or GAPDH. NF-κB (A), iNOS (B), and CYP3A (C) protein expression levels in rat liver were measured by western blot. NF-κB, iNOS, and CYP3A expression levels were quantified by ImageQuant software (GE Healthcare Life Science, Little Chalfont, UK). Data represent means ± SD of three independent experiments. Asterisks stars above bars indicate differences between groups.
    Rabbit Polyclonal Antibodies Against Cyp3a, 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 polyclonal antibodies against cyp3a/product/Boster Bio
    Average 90 stars, based on 1 article reviews
    rabbit polyclonal antibodies against cyp3a - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    rabbit polyclonal antibody against mouse cyp3a  (Enzo Biochem)
    90
    Enzo Biochem rabbit polyclonal antibody against mouse cyp3a
    Rats were treated with BCG (125 mg kg -1 , intravenously, once for 2 wks) or BCG + HRP (50, 100, or 200 mg kg -1 d -1 , oral administration for 13d). Liver proteins were extracted to determine NF-κB, iNOS, and <t>CYP3A</t> expression. Equal amounts (30 μg) of protein were subjected to SDS-PAGE followed by western blot analysis using anti-NF-κB, anti-iNOS, and anti-CYP3A antibodies. Results were normalized to LMNA or GAPDH. NF-κB (A), iNOS (B), and CYP3A (C) protein expression levels in rat liver were measured by western blot. NF-κB, iNOS, and CYP3A expression levels were quantified by ImageQuant software (GE Healthcare Life Science, Little Chalfont, UK). Data represent means ± SD of three independent experiments. Asterisks stars above bars indicate differences between groups.
    Rabbit Polyclonal Antibody Against Mouse Cyp3a, supplied by Enzo Biochem, 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 polyclonal antibody against mouse cyp3a/product/Enzo Biochem
    Average 90 stars, based on 1 article reviews
    rabbit polyclonal antibody against mouse cyp3a - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Rats were treated with BCG (125 mg kg -1 , intravenously, once for 2 wks) or BCG + HRP (50, 100, or 200 mg kg -1 d -1 , oral administration for 13d). Liver proteins were extracted to determine NF-κB, iNOS, and CYP3A expression. Equal amounts (30 μg) of protein were subjected to SDS-PAGE followed by western blot analysis using anti-NF-κB, anti-iNOS, and anti-CYP3A antibodies. Results were normalized to LMNA or GAPDH. NF-κB (A), iNOS (B), and CYP3A (C) protein expression levels in rat liver were measured by western blot. NF-κB, iNOS, and CYP3A expression levels were quantified by ImageQuant software (GE Healthcare Life Science, Little Chalfont, UK). Data represent means ± SD of three independent experiments. Asterisks stars above bars indicate differences between groups.

    Journal: PLoS ONE

    Article Title: Involvement of NF-κB in the reversal of CYP3A down-regulation induced by sea buckthorn in BCG-induced rats

    doi: 10.1371/journal.pone.0238810

    Figure Lengend Snippet: Rats were treated with BCG (125 mg kg -1 , intravenously, once for 2 wks) or BCG + HRP (50, 100, or 200 mg kg -1 d -1 , oral administration for 13d). Liver proteins were extracted to determine NF-κB, iNOS, and CYP3A expression. Equal amounts (30 μg) of protein were subjected to SDS-PAGE followed by western blot analysis using anti-NF-κB, anti-iNOS, and anti-CYP3A antibodies. Results were normalized to LMNA or GAPDH. NF-κB (A), iNOS (B), and CYP3A (C) protein expression levels in rat liver were measured by western blot. NF-κB, iNOS, and CYP3A expression levels were quantified by ImageQuant software (GE Healthcare Life Science, Little Chalfont, UK). Data represent means ± SD of three independent experiments. Asterisks stars above bars indicate differences between groups.

    Article Snippet: Kits for cytoplasmic and nuclear protein extraction, bicinchoninic acid (BCA) protein assay (No. AR0146), sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), rat IL-1β ELISA (No. BA2913), TNF-α ELISA (No. BA0527), and rabbit polyclonal antibodies against CYP3A (No. A00339), iNOS (No. EK0394), LMNA(Lamin A/C) (Cat. No. BA1227), and GAPDH (No. BA2913) were obtained from Wuhan Boster Biological Engineering Co. Ltd., Wuhan, China.

    Techniques: Expressing, SDS Page, Western Blot, Software

    Rats were treated with BCG (125 mg kg-1, intravenously, once for 2 wks) or BCG + HRP (50, 100, or 200 mg•kg -1 •d -1 , oral administration for 13d). The mRNA expression of CYP3A was measured by real-time PCR. Each bar represents the mean ± SD from three independent experiments (n = 10/group). Asterisks stars above bars indicate differences between groups. The significance of the data was determined by one-way analysis of variance (ANOVA) followed by Tukey’s test.

    Journal: PLoS ONE

    Article Title: Involvement of NF-κB in the reversal of CYP3A down-regulation induced by sea buckthorn in BCG-induced rats

    doi: 10.1371/journal.pone.0238810

    Figure Lengend Snippet: Rats were treated with BCG (125 mg kg-1, intravenously, once for 2 wks) or BCG + HRP (50, 100, or 200 mg•kg -1 •d -1 , oral administration for 13d). The mRNA expression of CYP3A was measured by real-time PCR. Each bar represents the mean ± SD from three independent experiments (n = 10/group). Asterisks stars above bars indicate differences between groups. The significance of the data was determined by one-way analysis of variance (ANOVA) followed by Tukey’s test.

    Article Snippet: Kits for cytoplasmic and nuclear protein extraction, bicinchoninic acid (BCA) protein assay (No. AR0146), sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), rat IL-1β ELISA (No. BA2913), TNF-α ELISA (No. BA0527), and rabbit polyclonal antibodies against CYP3A (No. A00339), iNOS (No. EK0394), LMNA(Lamin A/C) (Cat. No. BA1227), and GAPDH (No. BA2913) were obtained from Wuhan Boster Biological Engineering Co. Ltd., Wuhan, China.

    Techniques: Expressing, Real-time Polymerase Chain Reaction