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cmp  (ATCC)


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    Structured Review

    ATCC cmp
    Intracellular ROS production <t>of</t> <t>CIP</t> (A) and <t>CMP</t> (B) in MN and PMN leukocytes. Data (means ± S.D.) were expressed as percent of values in control cells of three independent experiments. *** p < 0.001 vs. control.
    Cmp, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 55486 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cmp/product/ATCC
    Average 99 stars, based on 55486 article reviews
    cmp - by Bioz Stars, 2026-05
    99/100 stars

    Images

    1) Product Images from "Evaluation of the protective effect of quercetin and luteolin against ciprofloxacin- and chloramphenicol-induced oxidative stress in blood cells and their impact on the microbiological activity"

    Article Title: Evaluation of the protective effect of quercetin and luteolin against ciprofloxacin- and chloramphenicol-induced oxidative stress in blood cells and their impact on the microbiological activity

    Journal: Frontiers in Pharmacology

    doi: 10.3389/fphar.2025.1626058

    Intracellular ROS production of CIP (A) and CMP (B) in MN and PMN leukocytes. Data (means ± S.D.) were expressed as percent of values in control cells of three independent experiments. *** p < 0.001 vs. control.
    Figure Legend Snippet: Intracellular ROS production of CIP (A) and CMP (B) in MN and PMN leukocytes. Data (means ± S.D.) were expressed as percent of values in control cells of three independent experiments. *** p < 0.001 vs. control.

    Techniques Used: Control

    Dose–response curves for Q, LT, and vitamin C on intracellular ROS produced by 16 μg/mL CIP (A) and 10 μg/mL CMP (B) in PMN human leukocytes.
    Figure Legend Snippet: Dose–response curves for Q, LT, and vitamin C on intracellular ROS produced by 16 μg/mL CIP (A) and 10 μg/mL CMP (B) in PMN human leukocytes.

    Techniques Used: Produced

    Effect of LT and Q on SOD enzyme activity in PMN human leukocytes exposed to CIP (A) and CMP (B) . Data (means ± S.D.) are expressed as SOD units per 10 6 cells of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.
    Figure Legend Snippet: Effect of LT and Q on SOD enzyme activity in PMN human leukocytes exposed to CIP (A) and CMP (B) . Data (means ± S.D.) are expressed as SOD units per 10 6 cells of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.

    Techniques Used: Activity Assay, Control

    Effect of LT and Q on CAT enzyme activity in PMN human leukocytes exposed to CIP (A) and CMP (B) . Data (means ± S.D.) are expressed as CAT units per 10 6 cells of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.
    Figure Legend Snippet: Effect of LT and Q on CAT enzyme activity in PMN human leukocytes exposed to CIP (A) and CMP (B) . Data (means ± S.D.) are expressed as CAT units per 10 6 cells of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.

    Techniques Used: Activity Assay, Control

    Effect of LT and Q on protein oxidation induced by CIP (A) and CMP (B) in PMN human leukocytes. Data (means ± S.D.) are expressed as µmol chloramine T per mg protein of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.
    Figure Legend Snippet: Effect of LT and Q on protein oxidation induced by CIP (A) and CMP (B) in PMN human leukocytes. Data (means ± S.D.) are expressed as µmol chloramine T per mg protein of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.

    Techniques Used: Control

    Quercetin (Q) and chloramphenicol (CMP) interaction by checkerboard assay. (A) Escherichia coli clinical strain resistant to CIP. (B) Staphylococcus aureus clinical strain resistant to CIP. (C) Escherichia coli ATCC 25922. (D) Staphylococcus aureus ATCC 29213.
    Figure Legend Snippet: Quercetin (Q) and chloramphenicol (CMP) interaction by checkerboard assay. (A) Escherichia coli clinical strain resistant to CIP. (B) Staphylococcus aureus clinical strain resistant to CIP. (C) Escherichia coli ATCC 25922. (D) Staphylococcus aureus ATCC 29213.

    Techniques Used:

    Luteolin (LT) and chloramphenicol (CMP) interaction by checkerboard assay. (A) Escherichia coli clinical strain resistant to CIP. (B) Staphylococcus aureus clinical strain resistant to CIP. (C) Escherichia coli ATCC 25922. (D) Staphylococcus aureus ATCC 29213.
    Figure Legend Snippet: Luteolin (LT) and chloramphenicol (CMP) interaction by checkerboard assay. (A) Escherichia coli clinical strain resistant to CIP. (B) Staphylococcus aureus clinical strain resistant to CIP. (C) Escherichia coli ATCC 25922. (D) Staphylococcus aureus ATCC 29213.

    Techniques Used:



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    Image Search Results


    Intracellular ROS production of CIP (A) and CMP (B) in MN and PMN leukocytes. Data (means ± S.D.) were expressed as percent of values in control cells of three independent experiments. *** p < 0.001 vs. control.

    Journal: Frontiers in Pharmacology

    Article Title: Evaluation of the protective effect of quercetin and luteolin against ciprofloxacin- and chloramphenicol-induced oxidative stress in blood cells and their impact on the microbiological activity

    doi: 10.3389/fphar.2025.1626058

    Figure Lengend Snippet: Intracellular ROS production of CIP (A) and CMP (B) in MN and PMN leukocytes. Data (means ± S.D.) were expressed as percent of values in control cells of three independent experiments. *** p < 0.001 vs. control.

    Article Snippet: Interactions between flavonoids and antibiotics were evaluated as described previously ( ) by checkerboard assay on Mueller-Hinton broth following the indications of . Four strains have been evaluated: two sensitive strains to CIP and CMP ( S. aureus ATCC 29213 and E. coli ATCC 25922), and two clinical strains ( S. aureus resistant to CIP and E. coli resistant to CIP).

    Techniques: Control

    Dose–response curves for Q, LT, and vitamin C on intracellular ROS produced by 16 μg/mL CIP (A) and 10 μg/mL CMP (B) in PMN human leukocytes.

    Journal: Frontiers in Pharmacology

    Article Title: Evaluation of the protective effect of quercetin and luteolin against ciprofloxacin- and chloramphenicol-induced oxidative stress in blood cells and their impact on the microbiological activity

    doi: 10.3389/fphar.2025.1626058

    Figure Lengend Snippet: Dose–response curves for Q, LT, and vitamin C on intracellular ROS produced by 16 μg/mL CIP (A) and 10 μg/mL CMP (B) in PMN human leukocytes.

    Article Snippet: Interactions between flavonoids and antibiotics were evaluated as described previously ( ) by checkerboard assay on Mueller-Hinton broth following the indications of . Four strains have been evaluated: two sensitive strains to CIP and CMP ( S. aureus ATCC 29213 and E. coli ATCC 25922), and two clinical strains ( S. aureus resistant to CIP and E. coli resistant to CIP).

    Techniques: Produced

    Effect of LT and Q on SOD enzyme activity in PMN human leukocytes exposed to CIP (A) and CMP (B) . Data (means ± S.D.) are expressed as SOD units per 10 6 cells of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.

    Journal: Frontiers in Pharmacology

    Article Title: Evaluation of the protective effect of quercetin and luteolin against ciprofloxacin- and chloramphenicol-induced oxidative stress in blood cells and their impact on the microbiological activity

    doi: 10.3389/fphar.2025.1626058

    Figure Lengend Snippet: Effect of LT and Q on SOD enzyme activity in PMN human leukocytes exposed to CIP (A) and CMP (B) . Data (means ± S.D.) are expressed as SOD units per 10 6 cells of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.

    Article Snippet: Interactions between flavonoids and antibiotics were evaluated as described previously ( ) by checkerboard assay on Mueller-Hinton broth following the indications of . Four strains have been evaluated: two sensitive strains to CIP and CMP ( S. aureus ATCC 29213 and E. coli ATCC 25922), and two clinical strains ( S. aureus resistant to CIP and E. coli resistant to CIP).

    Techniques: Activity Assay, Control

    Effect of LT and Q on CAT enzyme activity in PMN human leukocytes exposed to CIP (A) and CMP (B) . Data (means ± S.D.) are expressed as CAT units per 10 6 cells of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.

    Journal: Frontiers in Pharmacology

    Article Title: Evaluation of the protective effect of quercetin and luteolin against ciprofloxacin- and chloramphenicol-induced oxidative stress in blood cells and their impact on the microbiological activity

    doi: 10.3389/fphar.2025.1626058

    Figure Lengend Snippet: Effect of LT and Q on CAT enzyme activity in PMN human leukocytes exposed to CIP (A) and CMP (B) . Data (means ± S.D.) are expressed as CAT units per 10 6 cells of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.

    Article Snippet: Interactions between flavonoids and antibiotics were evaluated as described previously ( ) by checkerboard assay on Mueller-Hinton broth following the indications of . Four strains have been evaluated: two sensitive strains to CIP and CMP ( S. aureus ATCC 29213 and E. coli ATCC 25922), and two clinical strains ( S. aureus resistant to CIP and E. coli resistant to CIP).

    Techniques: Activity Assay, Control

    Effect of LT and Q on protein oxidation induced by CIP (A) and CMP (B) in PMN human leukocytes. Data (means ± S.D.) are expressed as µmol chloramine T per mg protein of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.

    Journal: Frontiers in Pharmacology

    Article Title: Evaluation of the protective effect of quercetin and luteolin against ciprofloxacin- and chloramphenicol-induced oxidative stress in blood cells and their impact on the microbiological activity

    doi: 10.3389/fphar.2025.1626058

    Figure Lengend Snippet: Effect of LT and Q on protein oxidation induced by CIP (A) and CMP (B) in PMN human leukocytes. Data (means ± S.D.) are expressed as µmol chloramine T per mg protein of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, statistical differences compared to control leukocytes; # p < 0.05, ## p < 0.01, ### p < 0.001, statistical differences compared to leukocytes treated with CIP or CMP.

    Article Snippet: Interactions between flavonoids and antibiotics were evaluated as described previously ( ) by checkerboard assay on Mueller-Hinton broth following the indications of . Four strains have been evaluated: two sensitive strains to CIP and CMP ( S. aureus ATCC 29213 and E. coli ATCC 25922), and two clinical strains ( S. aureus resistant to CIP and E. coli resistant to CIP).

    Techniques: Control

    Quercetin (Q) and chloramphenicol (CMP) interaction by checkerboard assay. (A) Escherichia coli clinical strain resistant to CIP. (B) Staphylococcus aureus clinical strain resistant to CIP. (C) Escherichia coli ATCC 25922. (D) Staphylococcus aureus ATCC 29213.

    Journal: Frontiers in Pharmacology

    Article Title: Evaluation of the protective effect of quercetin and luteolin against ciprofloxacin- and chloramphenicol-induced oxidative stress in blood cells and their impact on the microbiological activity

    doi: 10.3389/fphar.2025.1626058

    Figure Lengend Snippet: Quercetin (Q) and chloramphenicol (CMP) interaction by checkerboard assay. (A) Escherichia coli clinical strain resistant to CIP. (B) Staphylococcus aureus clinical strain resistant to CIP. (C) Escherichia coli ATCC 25922. (D) Staphylococcus aureus ATCC 29213.

    Article Snippet: Interactions between flavonoids and antibiotics were evaluated as described previously ( ) by checkerboard assay on Mueller-Hinton broth following the indications of . Four strains have been evaluated: two sensitive strains to CIP and CMP ( S. aureus ATCC 29213 and E. coli ATCC 25922), and two clinical strains ( S. aureus resistant to CIP and E. coli resistant to CIP).

    Techniques:

    Luteolin (LT) and chloramphenicol (CMP) interaction by checkerboard assay. (A) Escherichia coli clinical strain resistant to CIP. (B) Staphylococcus aureus clinical strain resistant to CIP. (C) Escherichia coli ATCC 25922. (D) Staphylococcus aureus ATCC 29213.

    Journal: Frontiers in Pharmacology

    Article Title: Evaluation of the protective effect of quercetin and luteolin against ciprofloxacin- and chloramphenicol-induced oxidative stress in blood cells and their impact on the microbiological activity

    doi: 10.3389/fphar.2025.1626058

    Figure Lengend Snippet: Luteolin (LT) and chloramphenicol (CMP) interaction by checkerboard assay. (A) Escherichia coli clinical strain resistant to CIP. (B) Staphylococcus aureus clinical strain resistant to CIP. (C) Escherichia coli ATCC 25922. (D) Staphylococcus aureus ATCC 29213.

    Article Snippet: Interactions between flavonoids and antibiotics were evaluated as described previously ( ) by checkerboard assay on Mueller-Hinton broth following the indications of . Four strains have been evaluated: two sensitive strains to CIP and CMP ( S. aureus ATCC 29213 and E. coli ATCC 25922), and two clinical strains ( S. aureus resistant to CIP and E. coli resistant to CIP).

    Techniques: