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df1513  (Bio-Rad)


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    Structured Review

    Bio-Rad df1513
    Df1513, supplied by Bio-Rad, 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/result/df1513/product/Bio-Rad
    Average 93 stars, based on 16 article reviews
    df1513 - by Bioz Stars, 2026-03
    93/100 stars

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    The effect of NO on iron handling genes in syncytialized BeWo cells. ( A – E ), qPCR results, and ( E – J ) protein analyses. Representative blots are shown in ( K ). HO-1 and HAMP mRNA levels are significantly increased in the group treated with NO compared to the untreated controls. Protein abundance of HO-1 is significantly increased in the group treated with NO compared to the untreated controls. No significant change in expression is seen in the rest of the genes studied. HO-1: heme oxygenase 1, HAMP: hepcidin antimicrobial peptide, TfR: <t>transferrin</t> receptor, DMT1: divalent metal transporter 1, FPN: ferroportin 1. Data are reported from at least three independent experiments as mean ± SD, ** p < 0.01, **** p < 0.0001, ns = not significant.
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    The effect of NO on iron handling genes in syncytialized BeWo cells. ( A – E ), qPCR results, and ( E – J ) protein analyses. Representative blots are shown in ( K ). HO-1 and HAMP mRNA levels are significantly increased in the group treated with NO compared to the untreated controls. Protein abundance of HO-1 is significantly increased in the group treated with NO compared to the untreated controls. No significant change in expression is seen in the rest of the genes studied. HO-1: heme oxygenase 1, HAMP: hepcidin antimicrobial peptide, TfR: transferrin receptor, DMT1: divalent metal transporter 1, FPN: ferroportin 1. Data are reported from at least three independent experiments as mean ± SD, ** p < 0.01, **** p < 0.0001, ns = not significant.

    Journal: International Journal of Molecular Sciences

    Article Title: Nitric Oxide Affects Heme Oxygenase-1, Hepcidin, and Transferrin Receptor Expression in the Placenta

    doi: 10.3390/ijms24065887

    Figure Lengend Snippet: The effect of NO on iron handling genes in syncytialized BeWo cells. ( A – E ), qPCR results, and ( E – J ) protein analyses. Representative blots are shown in ( K ). HO-1 and HAMP mRNA levels are significantly increased in the group treated with NO compared to the untreated controls. Protein abundance of HO-1 is significantly increased in the group treated with NO compared to the untreated controls. No significant change in expression is seen in the rest of the genes studied. HO-1: heme oxygenase 1, HAMP: hepcidin antimicrobial peptide, TfR: transferrin receptor, DMT1: divalent metal transporter 1, FPN: ferroportin 1. Data are reported from at least three independent experiments as mean ± SD, ** p < 0.01, **** p < 0.0001, ns = not significant.

    Article Snippet: The antibodies used were actin (catalog #3700S) and HO-1 (catalog #70081S) from Cell Signaling Technologies (Danvers, MA, USA); transferrin (catalog #NB500-418), ferroportin (catalog #NBP1-21502), and transferrin receptor (catalog #NBP2-32945) from Novus Biologicals (Centennial, CO, USA); DMT (catalog #PA5-35136) from Thermo Fisher Scientific (Waltham, MA, USA); and hepcidin (catalog #SAB1405228) from Sigma-Aldrich (St. Louis, MO, USA).

    Techniques: Quantitative Proteomics, Expressing

    The effect of NO on iron handling gene expression in human placental villous explants. ( A – E ) qPCR results, ( F – J ) protein analyses. Representative blots are shown in ( K ). HO-1 and TfR mRNA levels are significantly increased in the group treated with NO compared to the untreated controls. Protein abundance of HO-1 is significantly increased in the group treated with NO compared to the untreated controls. No significant change in expression is seen in the rest of the genes studied. HO-1: heme oxygenase 1, HAMP: hepcidin antimicrobial peptide, TfR: transferrin receptor, DMT1: divalent metal transporter 1, FPN: ferroportin 1. Data are reported from at least three independent experiments as mean ± SD, *** p < 0.001, ns = not significant.

    Journal: International Journal of Molecular Sciences

    Article Title: Nitric Oxide Affects Heme Oxygenase-1, Hepcidin, and Transferrin Receptor Expression in the Placenta

    doi: 10.3390/ijms24065887

    Figure Lengend Snippet: The effect of NO on iron handling gene expression in human placental villous explants. ( A – E ) qPCR results, ( F – J ) protein analyses. Representative blots are shown in ( K ). HO-1 and TfR mRNA levels are significantly increased in the group treated with NO compared to the untreated controls. Protein abundance of HO-1 is significantly increased in the group treated with NO compared to the untreated controls. No significant change in expression is seen in the rest of the genes studied. HO-1: heme oxygenase 1, HAMP: hepcidin antimicrobial peptide, TfR: transferrin receptor, DMT1: divalent metal transporter 1, FPN: ferroportin 1. Data are reported from at least three independent experiments as mean ± SD, *** p < 0.001, ns = not significant.

    Article Snippet: The antibodies used were actin (catalog #3700S) and HO-1 (catalog #70081S) from Cell Signaling Technologies (Danvers, MA, USA); transferrin (catalog #NB500-418), ferroportin (catalog #NBP1-21502), and transferrin receptor (catalog #NBP2-32945) from Novus Biologicals (Centennial, CO, USA); DMT (catalog #PA5-35136) from Thermo Fisher Scientific (Waltham, MA, USA); and hepcidin (catalog #SAB1405228) from Sigma-Aldrich (St. Louis, MO, USA).

    Techniques: Gene Expression, Quantitative Proteomics, Expressing

    The effect of hypoxia on iron handling genes in response to NO in syncitialized BeWo cells (SCTs). ( A – F ) qPCR results and ( G – K ) protein analyses. Representative blots are shown in ( K ). Hypoxia alone did not significantly alter mRNA or protein levels of any of the studied iron homeostasis markers compared to normoxic controls. ( A , B ) The combination of hypoxia and NO resulted in a significant increase in HO-1 and HAMP mRNA levels, while NO increased HAMP mRNA levels significantly under hypoxic conditions. No significant effect of hypoxia or NO was seen in any of the other targets studied. HO-1: Heme Oxygenase 1, HAMP: Hepcidin antimicrobial peptide, TfR: Transferrin Receptor, TF: Transferrin, DMT1, Divalent metal transporter 1, FPN: Ferroportin 1. Data are reported from at least three independent experiments as mean ± SD, * p < 0.05, ns = not significant.

    Journal: International Journal of Molecular Sciences

    Article Title: Nitric Oxide Affects Heme Oxygenase-1, Hepcidin, and Transferrin Receptor Expression in the Placenta

    doi: 10.3390/ijms24065887

    Figure Lengend Snippet: The effect of hypoxia on iron handling genes in response to NO in syncitialized BeWo cells (SCTs). ( A – F ) qPCR results and ( G – K ) protein analyses. Representative blots are shown in ( K ). Hypoxia alone did not significantly alter mRNA or protein levels of any of the studied iron homeostasis markers compared to normoxic controls. ( A , B ) The combination of hypoxia and NO resulted in a significant increase in HO-1 and HAMP mRNA levels, while NO increased HAMP mRNA levels significantly under hypoxic conditions. No significant effect of hypoxia or NO was seen in any of the other targets studied. HO-1: Heme Oxygenase 1, HAMP: Hepcidin antimicrobial peptide, TfR: Transferrin Receptor, TF: Transferrin, DMT1, Divalent metal transporter 1, FPN: Ferroportin 1. Data are reported from at least three independent experiments as mean ± SD, * p < 0.05, ns = not significant.

    Article Snippet: The antibodies used were actin (catalog #3700S) and HO-1 (catalog #70081S) from Cell Signaling Technologies (Danvers, MA, USA); transferrin (catalog #NB500-418), ferroportin (catalog #NBP1-21502), and transferrin receptor (catalog #NBP2-32945) from Novus Biologicals (Centennial, CO, USA); DMT (catalog #PA5-35136) from Thermo Fisher Scientific (Waltham, MA, USA); and hepcidin (catalog #SAB1405228) from Sigma-Aldrich (St. Louis, MO, USA).

    Techniques:

    Primer sequences.

    Journal: PLoS ONE

    Article Title: Evidence for a Lack of a Direct Transcriptional Suppression of the Iron Regulatory Peptide Hepcidin by Hypoxia-Inducible Factors

    doi: 10.1371/journal.pone.0007875

    Figure Lengend Snippet: Primer sequences.

    Article Snippet: Immunoblotting for HIF-1α (rabbit antiserum NB100–449, Novus Biologicals, USA), HIF-2α (mouse monoclonal antibody (mab) NB100–132) and transferrin receptor 1 (mab DF1513, Sigma) was performed as described previously .

    Techniques: Clone Assay, Construct, Quantitative RT-PCR