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rh α gala  (R&D Systems)


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    Structured Review

    R&D Systems rh α gala
    FD patients’ cohort description. Activity of <t> α-GalA </t> (μmol/hL) was measured in dried blood spots (DBSs) at enrollment in the study. NT indicates non-treated FD patient. ERT = enzyme replacement therapy, PC = pharmacological chaperone. N.D. = not available, N.A. = not applicable.
    Rh α Gala, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rh α gala/product/R&D Systems
    Average 93 stars, based on 11 article reviews
    rh α gala - by Bioz Stars, 2026-03
    93/100 stars

    Images

    1) Product Images from "Inflammatory and Cardiovascular Biomarkers to Monitor Fabry Disease Progression"

    Article Title: Inflammatory and Cardiovascular Biomarkers to Monitor Fabry Disease Progression

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms25116024

    FD patients’ cohort description. Activity of α-GalA (μmol/hL) was measured in dried blood spots (DBSs) at enrollment in the study. NT indicates non-treated FD patient. ERT = enzyme replacement therapy, PC = pharmacological chaperone. N.D. = not available, N.A. = not applicable.
    Figure Legend Snippet: FD patients’ cohort description. Activity of α-GalA (μmol/hL) was measured in dried blood spots (DBSs) at enrollment in the study. NT indicates non-treated FD patient. ERT = enzyme replacement therapy, PC = pharmacological chaperone. N.D. = not available, N.A. = not applicable.

    Techniques Used: Activity Assay, Mutagenesis

    Plasmatic activity levels. Histograms n panel ( A ) represent plasmatic α-GalA activity ± SEM (nmol/mL·h) in controls (white bars), FD naïve patients (light gray bars), and FD patients treated with ERT (white bars with dots). In panel ( B ), α-GalA activity values are separated according to sex. Significance was assessed by one-way ANOVA non-parametric test, Kruskal–Wallis multiple comparisons (* p < 0.05).
    Figure Legend Snippet: Plasmatic activity levels. Histograms n panel ( A ) represent plasmatic α-GalA activity ± SEM (nmol/mL·h) in controls (white bars), FD naïve patients (light gray bars), and FD patients treated with ERT (white bars with dots). In panel ( B ), α-GalA activity values are separated according to sex. Significance was assessed by one-way ANOVA non-parametric test, Kruskal–Wallis multiple comparisons (* p < 0.05).

    Techniques Used: Activity Assay

    Anti-α-GalA-IgG antibody concentration. Concentration of IgG antibodies determined by ELISA in plasma samples of control individuals and patients in treatment or not with ERT, collected at Ti, T6, T12 months. ( A ) Average values (mean ± SEM) for each group of patients at each collection time. ( B ) Individual values (mean of two replicates) for each subject of the study at all assessed times. ( C ) Time course of anti-α-GalA antibodies for the four patients in panel ( B ), who presented antibody levels close or above the threshold. In all graphs, dotted lines represent threshold.
    Figure Legend Snippet: Anti-α-GalA-IgG antibody concentration. Concentration of IgG antibodies determined by ELISA in plasma samples of control individuals and patients in treatment or not with ERT, collected at Ti, T6, T12 months. ( A ) Average values (mean ± SEM) for each group of patients at each collection time. ( B ) Individual values (mean of two replicates) for each subject of the study at all assessed times. ( C ) Time course of anti-α-GalA antibodies for the four patients in panel ( B ), who presented antibody levels close or above the threshold. In all graphs, dotted lines represent threshold.

    Techniques Used: Concentration Assay, Enzyme-linked Immunosorbent Assay, Control



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    FD patients’ cohort description. Activity of <t> α-GalA </t> (μmol/hL) was measured in dried blood spots (DBSs) at enrollment in the study. NT indicates non-treated FD patient. ERT = enzyme replacement therapy, PC = pharmacological chaperone. N.D. = not available, N.A. = not applicable.
    Rh α Gala, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    FD patients’ cohort description. Activity of <t> α-GalA </t> (μmol/hL) was measured in dried blood spots (DBSs) at enrollment in the study. NT indicates non-treated FD patient. ERT = enzyme replacement therapy, PC = pharmacological chaperone. N.D. = not available, N.A. = not applicable.
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    Image Search Results


    FD patients’ cohort description. Activity of α-GalA (μmol/hL) was measured in dried blood spots (DBSs) at enrollment in the study. NT indicates non-treated FD patient. ERT = enzyme replacement therapy, PC = pharmacological chaperone. N.D. = not available, N.A. = not applicable.

    Journal: International Journal of Molecular Sciences

    Article Title: Inflammatory and Cardiovascular Biomarkers to Monitor Fabry Disease Progression

    doi: 10.3390/ijms25116024

    Figure Lengend Snippet: FD patients’ cohort description. Activity of α-GalA (μmol/hL) was measured in dried blood spots (DBSs) at enrollment in the study. NT indicates non-treated FD patient. ERT = enzyme replacement therapy, PC = pharmacological chaperone. N.D. = not available, N.A. = not applicable.

    Article Snippet: Briefly, plates were coated with rh-α-GalA (#6146-GH, R&D, Systems), which binds to IgG antibodies against the α-GalA recombinant enzyme (diluted 1:50 in PBS with 5% low fat milk).

    Techniques: Activity Assay, Mutagenesis

    Plasmatic activity levels. Histograms n panel ( A ) represent plasmatic α-GalA activity ± SEM (nmol/mL·h) in controls (white bars), FD naïve patients (light gray bars), and FD patients treated with ERT (white bars with dots). In panel ( B ), α-GalA activity values are separated according to sex. Significance was assessed by one-way ANOVA non-parametric test, Kruskal–Wallis multiple comparisons (* p < 0.05).

    Journal: International Journal of Molecular Sciences

    Article Title: Inflammatory and Cardiovascular Biomarkers to Monitor Fabry Disease Progression

    doi: 10.3390/ijms25116024

    Figure Lengend Snippet: Plasmatic activity levels. Histograms n panel ( A ) represent plasmatic α-GalA activity ± SEM (nmol/mL·h) in controls (white bars), FD naïve patients (light gray bars), and FD patients treated with ERT (white bars with dots). In panel ( B ), α-GalA activity values are separated according to sex. Significance was assessed by one-way ANOVA non-parametric test, Kruskal–Wallis multiple comparisons (* p < 0.05).

    Article Snippet: Briefly, plates were coated with rh-α-GalA (#6146-GH, R&D, Systems), which binds to IgG antibodies against the α-GalA recombinant enzyme (diluted 1:50 in PBS with 5% low fat milk).

    Techniques: Activity Assay

    Anti-α-GalA-IgG antibody concentration. Concentration of IgG antibodies determined by ELISA in plasma samples of control individuals and patients in treatment or not with ERT, collected at Ti, T6, T12 months. ( A ) Average values (mean ± SEM) for each group of patients at each collection time. ( B ) Individual values (mean of two replicates) for each subject of the study at all assessed times. ( C ) Time course of anti-α-GalA antibodies for the four patients in panel ( B ), who presented antibody levels close or above the threshold. In all graphs, dotted lines represent threshold.

    Journal: International Journal of Molecular Sciences

    Article Title: Inflammatory and Cardiovascular Biomarkers to Monitor Fabry Disease Progression

    doi: 10.3390/ijms25116024

    Figure Lengend Snippet: Anti-α-GalA-IgG antibody concentration. Concentration of IgG antibodies determined by ELISA in plasma samples of control individuals and patients in treatment or not with ERT, collected at Ti, T6, T12 months. ( A ) Average values (mean ± SEM) for each group of patients at each collection time. ( B ) Individual values (mean of two replicates) for each subject of the study at all assessed times. ( C ) Time course of anti-α-GalA antibodies for the four patients in panel ( B ), who presented antibody levels close or above the threshold. In all graphs, dotted lines represent threshold.

    Article Snippet: Briefly, plates were coated with rh-α-GalA (#6146-GH, R&D, Systems), which binds to IgG antibodies against the α-GalA recombinant enzyme (diluted 1:50 in PBS with 5% low fat milk).

    Techniques: Concentration Assay, Enzyme-linked Immunosorbent Assay, Control