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anti cbr1  (Santa Cruz Biotechnology)


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    Santa Cruz Biotechnology anti cbr1
    Anti Cbr1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 16 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/100518-1/Carbonyl+reductase+1+Antibody/10__3390_slash_app9245552-67-5-13
    Average 93 stars, based on 16 article reviews
    anti cbr1 - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Bioprocessing:

    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.
    Article Snippet: The RevertAidTM H Minus First Strand cDNA Synthesis Kit, the Absolute QPCR SYBR Green Mix, the PierceTM BCA Protein Assay Kit, the Pierce ECL Western Blotting Substrate, the secondary HRP-conjugated antirabbit antibody, 2’-hydroxy-flavanone (2-OH-flavanone), and the RIPA buffer were purchased from Thermo Fisher Scientific (Waltham, MA, USA). .. 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). .. The secondary HRP-conjugated goat anti-Mouse IgG was from GE Healthcare (Chicago, IL, USA).

    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
    Article Snippet: The RevertAidTM H Minus First Strand cDNA Synthesis Kit, the Absolute QPCR SYBR Green Mix, the PierceTM BCA Protein Assay Kit, the Pierce ECL Western Blotting Substrate, the secondary HRP-conjugated anti-rabbit antibody, 2’-hydroxy-flavanone (2-OH-flavanone), and the RIPA buffer were purchased from Thermo Fisher Scientific (Waltham, MA, USA). .. 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). .. The secondary HRP-conjugated goat anti-Mouse IgG was from GE Healthcare (Chicago, IL, USA).

    other:

    Article Title: Effects of cellular differentiation in human primary bronchial epithelial cells: Metabolism of 4-(methylnitrosamine)-1-(3-pyridyl)-1-butanone
    Article Snippet: All analyses were conducted using GraphPad Prism (La Jolla, CA).



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    Western blot of the AKR1B1, AKR1A1, AKR1C3, <t>CBR1,</t> 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
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    Western blot of the AKR1B1, AKR1A1, AKR1C3, <t>CBR1,</t> 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
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    Western blot of the AKR1B1, AKR1A1, AKR1C3, <t>CBR1,</t> 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
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    Primers for the qRT-PCR.
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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