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human holo transferrin  (Beyotime)


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    Beyotime human holo transferrin
    Human Holo Transferrin, supplied by Beyotime, 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/product/human+holo+transferrin/annexin+v+fitc+apoptosis+detection+kit/pm39826335-189-0-24
    Average 90 stars, based on 1 article reviews
    human holo transferrin - by Bioz Stars, 2026-09
    90/100 stars

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    (A). Experimental design for the assessment of iron in murine T-cells that were exposed to iron media conditions ranging from 0.001mg/mL – 0.625mg/mL <t>holotransferrin;</t> (B). Histograms showing the mass-frequency distributions of iron mass/cell for each holotransferrin condition from cells taken from each of three mice. Mass distributions are shown in attograms (ag) (10 -18 g). Geometric means (GM) of each population are annotated per facet; (C). Correlation plot presenting the geometric means from each distribution versus the iron condition for each mouse (with a log 10 x-axis). Logarithmic trend lines, associated equations and R 2 values are displayed for each profile. Error bars show the 95 th confidence intervals; (D). Line plots showing the mean iron mass/cell per tenth percentile for each holotransferrin condition from each mouse; (E). Line plots presenting proportions of cell proliferation activity per iron condition (percentage of total cells dividing 0, 1 or 2+ times) with log 10 x-axes from each mouse; (F). Line plot presenting the mean total amount of iron consumed by the cells from the three mice for each iron condition (with a log 10 x-axis). Error bars show the range of total iron calculated per mouse; (G). Scatter plot presenting the inverse correlation between the magnitude of cell proliferation during the live culturing period against the skewness of the single cell metallomic distributions for iron.
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    (A). Experimental design for the assessment of iron in murine T-cells that were exposed to iron media conditions ranging from 0.001mg/mL – 0.625mg/mL <t>holotransferrin;</t> (B). Histograms showing the mass-frequency distributions of iron mass/cell for each holotransferrin condition from cells taken from each of three mice. Mass distributions are shown in attograms (ag) (10 -18 g). Geometric means (GM) of each population are annotated per facet; (C). Correlation plot presenting the geometric means from each distribution versus the iron condition for each mouse (with a log 10 x-axis). Logarithmic trend lines, associated equations and R 2 values are displayed for each profile. Error bars show the 95 th confidence intervals; (D). Line plots showing the mean iron mass/cell per tenth percentile for each holotransferrin condition from each mouse; (E). Line plots presenting proportions of cell proliferation activity per iron condition (percentage of total cells dividing 0, 1 or 2+ times) with log 10 x-axes from each mouse; (F). Line plot presenting the mean total amount of iron consumed by the cells from the three mice for each iron condition (with a log 10 x-axis). Error bars show the range of total iron calculated per mouse; (G). Scatter plot presenting the inverse correlation between the magnitude of cell proliferation during the live culturing period against the skewness of the single cell metallomic distributions for iron.
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    Image Search Results


    (A). Experimental design for the assessment of iron in murine T-cells that were exposed to iron media conditions ranging from 0.001mg/mL – 0.625mg/mL holotransferrin; (B). Histograms showing the mass-frequency distributions of iron mass/cell for each holotransferrin condition from cells taken from each of three mice. Mass distributions are shown in attograms (ag) (10 -18 g). Geometric means (GM) of each population are annotated per facet; (C). Correlation plot presenting the geometric means from each distribution versus the iron condition for each mouse (with a log 10 x-axis). Logarithmic trend lines, associated equations and R 2 values are displayed for each profile. Error bars show the 95 th confidence intervals; (D). Line plots showing the mean iron mass/cell per tenth percentile for each holotransferrin condition from each mouse; (E). Line plots presenting proportions of cell proliferation activity per iron condition (percentage of total cells dividing 0, 1 or 2+ times) with log 10 x-axes from each mouse; (F). Line plot presenting the mean total amount of iron consumed by the cells from the three mice for each iron condition (with a log 10 x-axis). Error bars show the range of total iron calculated per mouse; (G). Scatter plot presenting the inverse correlation between the magnitude of cell proliferation during the live culturing period against the skewness of the single cell metallomic distributions for iron.

    Journal: bioRxiv

    Article Title: Cell-type specific iron content regulation revealed by single-cell iron quantification

    doi: 10.1101/2025.06.22.660918

    Figure Lengend Snippet: (A). Experimental design for the assessment of iron in murine T-cells that were exposed to iron media conditions ranging from 0.001mg/mL – 0.625mg/mL holotransferrin; (B). Histograms showing the mass-frequency distributions of iron mass/cell for each holotransferrin condition from cells taken from each of three mice. Mass distributions are shown in attograms (ag) (10 -18 g). Geometric means (GM) of each population are annotated per facet; (C). Correlation plot presenting the geometric means from each distribution versus the iron condition for each mouse (with a log 10 x-axis). Logarithmic trend lines, associated equations and R 2 values are displayed for each profile. Error bars show the 95 th confidence intervals; (D). Line plots showing the mean iron mass/cell per tenth percentile for each holotransferrin condition from each mouse; (E). Line plots presenting proportions of cell proliferation activity per iron condition (percentage of total cells dividing 0, 1 or 2+ times) with log 10 x-axes from each mouse; (F). Line plot presenting the mean total amount of iron consumed by the cells from the three mice for each iron condition (with a log 10 x-axis). Error bars show the range of total iron calculated per mouse; (G). Scatter plot presenting the inverse correlation between the magnitude of cell proliferation during the live culturing period against the skewness of the single cell metallomic distributions for iron.

    Article Snippet: Human holotransferrin (R&D systems, 2914-HT-001G) was added at concentrations of 0.001 mg/mL to 0.625 mg/mL.

    Techniques: Activity Assay

    (A). Mean fluorescence intensity (MFI) of CD71 (transferrin receptor) versus the geometric mean single cell Fe content (ag) for each population distribution, from each holotransferrin condition; (B). Mean fluorescence intensity (MFI) of CD25 (alpha chain component of the IL-2 surface receptor on T-cells) versus the geometric mean single cell Fe content (ag) for each population distribution, from each holotransferrin condition; (C). Mean fluorescence intensity (MFI) of CD71 versus the geometric mean single cell Ca content (ag) for each population distribution, from each holotransferrin condition; (D). Mean fluorescence intensity (MFI) of CD25 versus the geometric mean single cell Ca content (ag) for each population distribution, from each holotransferrin condition. Error bars present the 95 th confidence intervals for each metallomic distribution determined by sc-ICP-MS.

    Journal: bioRxiv

    Article Title: Cell-type specific iron content regulation revealed by single-cell iron quantification

    doi: 10.1101/2025.06.22.660918

    Figure Lengend Snippet: (A). Mean fluorescence intensity (MFI) of CD71 (transferrin receptor) versus the geometric mean single cell Fe content (ag) for each population distribution, from each holotransferrin condition; (B). Mean fluorescence intensity (MFI) of CD25 (alpha chain component of the IL-2 surface receptor on T-cells) versus the geometric mean single cell Fe content (ag) for each population distribution, from each holotransferrin condition; (C). Mean fluorescence intensity (MFI) of CD71 versus the geometric mean single cell Ca content (ag) for each population distribution, from each holotransferrin condition; (D). Mean fluorescence intensity (MFI) of CD25 versus the geometric mean single cell Ca content (ag) for each population distribution, from each holotransferrin condition. Error bars present the 95 th confidence intervals for each metallomic distribution determined by sc-ICP-MS.

    Article Snippet: Human holotransferrin (R&D systems, 2914-HT-001G) was added at concentrations of 0.001 mg/mL to 0.625 mg/mL.

    Techniques: Fluorescence