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rabbit anti carbonyl reductase 1 antibody  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology rabbit anti carbonyl reductase 1 antibody
    Primers for the qRT-PCR.
    Rabbit Anti Carbonyl Reductase 1 Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/100518-1/pmc07953429-140-0-11?v=Santa+Cruz+Biotechnology
    Average 93 stars, based on 15 article reviews
    rabbit anti carbonyl reductase 1 antibody - by Bioz Stars, 2026-08
    93/100 stars

    Images

    1) Product Images from "Effects of cellular differentiation in human primary bronchial epithelial cells: Metabolism of 4-(methylnitrosamine)-1-(3-pyridyl)-1-butanone"

    Article Title: Effects of cellular differentiation in human primary bronchial epithelial cells: Metabolism of 4-(methylnitrosamine)-1-(3-pyridyl)-1-butanone

    Journal: Toxicology in vitro : an international journal published in association with BIBRA

    doi: 10.1016/j.tiv.2018.12.006

    Primers for the qRT-PCR.
    Figure Legend Snippet: Primers for the qRT-PCR.

    Techniques Used: Amplification

    Protein expression of the major metabolic enzymes implicated in NNK metabolism. Protein expressions of CYP2A6/2A13 and carbonyl reductase 1 were analyzed using immunoblotting in NHBE cells and ALI cultures. β-Actin was used as the loading control.
    Figure Legend Snippet: Protein expression of the major metabolic enzymes implicated in NNK metabolism. Protein expressions of CYP2A6/2A13 and carbonyl reductase 1 were analyzed using immunoblotting in NHBE cells and ALI cultures. β-Actin was used as the loading control.

    Techniques Used: Expressing, Western Blot



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    Image Search Results


    Western blot of the AKR1B1, AKR1A1, AKR1C3, CBR1, and CBR3 in HepG2, MCF-7, and HEK293 cells. β-actin served as a loading control. Depicted is one blot of a series of three for each protein investigated

    Journal: Archives of Toxicology

    Article Title: In vitro evaluation of the reductive carbonyl idarubicin metabolism to evaluate inhibitors of the formation of cardiotoxic idarubicinol via carbonyl and aldo–keto reductases

    doi: 10.1007/s00204-023-03661-7

    Figure Lengend Snippet: Western blot of the AKR1B1, AKR1A1, AKR1C3, CBR1, and CBR3 in HepG2, MCF-7, and HEK293 cells. β-actin served as a loading control. Depicted is one blot of a series of three for each protein investigated

    Article Snippet: The mouse monoclonal antibodies against β-actin (sc-47778), AKR1B1 (aldose reductase (H-6, sc-166918)), CBR1 (B-11, sc-390554), and CBR3 (E-12, sc-374393) were obtained from Santa Cruz (Heidelberg, Germany), the rabbit monoclonal antibody against AKR1C3 (ab209899) and the rabbit polyclonal antibody against AKR1A1 (ab125878) were from Abcam (Cambridge, United Kingdom).

    Techniques: Western Blot, Control

    Inhibition of idarubicinol formation by different inhibitors in HEK293, HepG2, and MCF-7 cells

    Journal: Archives of Toxicology

    Article Title: In vitro evaluation of the reductive carbonyl idarubicin metabolism to evaluate inhibitors of the formation of cardiotoxic idarubicinol via carbonyl and aldo–keto reductases

    doi: 10.1007/s00204-023-03661-7

    Figure Lengend Snippet: Inhibition of idarubicinol formation by different inhibitors in HEK293, HepG2, and MCF-7 cells

    Article Snippet: The mouse monoclonal antibodies against β-actin (sc-47778), AKR1B1 (aldose reductase (H-6, sc-166918)), CBR1 (B-11, sc-390554), and CBR3 (E-12, sc-374393) were obtained from Santa Cruz (Heidelberg, Germany), the rabbit monoclonal antibody against AKR1C3 (ab209899) and the rabbit polyclonal antibody against AKR1A1 (ab125878) were from Abcam (Cambridge, United Kingdom).

    Techniques: Inhibition

    Expression of the mRNA of the five reductases in human liver samples and HepG2 cells. mRNA expression of AKR1A1, AKR1B1, AKR1C3, CBR1 , and CBR3 was quantified in 7 human liver samples and HepG2 cells via real-time RT-PCR and normalized to the expression of the two housekeeping genes HUPO and RPL13 . Each data point for the liver samples represents the mean of a technical duplicate and the data for the HepG2 cells represent the mean ± S.E.M. for n = 7

    Journal: Archives of Toxicology

    Article Title: In vitro evaluation of the reductive carbonyl idarubicin metabolism to evaluate inhibitors of the formation of cardiotoxic idarubicinol via carbonyl and aldo–keto reductases

    doi: 10.1007/s00204-023-03661-7

    Figure Lengend Snippet: Expression of the mRNA of the five reductases in human liver samples and HepG2 cells. mRNA expression of AKR1A1, AKR1B1, AKR1C3, CBR1 , and CBR3 was quantified in 7 human liver samples and HepG2 cells via real-time RT-PCR and normalized to the expression of the two housekeeping genes HUPO and RPL13 . Each data point for the liver samples represents the mean of a technical duplicate and the data for the HepG2 cells represent the mean ± S.E.M. for n = 7

    Article Snippet: The mouse monoclonal antibodies against β-actin (sc-47778), AKR1B1 (aldose reductase (H-6, sc-166918)), CBR1 (B-11, sc-390554), and CBR3 (E-12, sc-374393) were obtained from Santa Cruz (Heidelberg, Germany), the rabbit monoclonal antibody against AKR1C3 (ab209899) and the rabbit polyclonal antibody against AKR1A1 (ab125878) were from Abcam (Cambridge, United Kingdom).

    Techniques: Expressing, Quantitative RT-PCR

    Primers for the qRT-PCR.

    Journal: Toxicology in vitro : an international journal published in association with BIBRA

    Article Title: Effects of cellular differentiation in human primary bronchial epithelial cells: Metabolism of 4-(methylnitrosamine)-1-(3-pyridyl)-1-butanone

    doi: 10.1016/j.tiv.2018.12.006

    Figure Lengend Snippet: Primers for the qRT-PCR.

    Article Snippet: Rabbit anti-carbonyl reductase 1 antibody and mouse anti-GAPDH were purchased from Santa Cruz Biotechnology (Dallas, TX).

    Techniques: Amplification

    Protein expression of the major metabolic enzymes implicated in NNK metabolism. Protein expressions of CYP2A6/2A13 and carbonyl reductase 1 were analyzed using immunoblotting in NHBE cells and ALI cultures. β-Actin was used as the loading control.

    Journal: Toxicology in vitro : an international journal published in association with BIBRA

    Article Title: Effects of cellular differentiation in human primary bronchial epithelial cells: Metabolism of 4-(methylnitrosamine)-1-(3-pyridyl)-1-butanone

    doi: 10.1016/j.tiv.2018.12.006

    Figure Lengend Snippet: Protein expression of the major metabolic enzymes implicated in NNK metabolism. Protein expressions of CYP2A6/2A13 and carbonyl reductase 1 were analyzed using immunoblotting in NHBE cells and ALI cultures. β-Actin was used as the loading control.

    Article Snippet: Rabbit anti-carbonyl reductase 1 antibody and mouse anti-GAPDH were purchased from Santa Cruz Biotechnology (Dallas, TX).

    Techniques: Expressing, Western Blot