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ifnar2 antibody  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec ifnar2 antibody
    Ifnar2 Antibody, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ifnar2+antibody/IFNAR2+Antibody%2C+anti-human%2C+REAfinity/pm41596638-249-18-21
    Average 94 stars, based on 22 article reviews
    ifnar2 antibody - by Bioz Stars, 2026-09
    94/100 stars

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    Article Title: IFNAR2 p.F8S Variant Associates with Severe COVID-19 and Adaptive Immune Cell Activation Modulation.
    Article Snippet: .. All reagents, instrument and software were from BD (Becton Dickinson Biosciences, BD, Franklin Lakes, NJ, USA), except the IFNAR2 antibody from Miltenyi Biotec (Miltenyi Biotec, Bergisch Gladbach, Germany). ..

    Article Title: IFNAR2 p.F8S Variant Associates with Severe COVID-19 and Adaptive Immune Cell Activation Modulation
    Article Snippet: .. All reagents, instrument and software were from BD (Becton Dickinson Biosciences, BD, Franklin Lakes, NJ, USA), except the IFNAR2 antibody from Miltenyi Biotec (Miltenyi Biotec, Bergisch Gladbach, Germany). ..



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    JAK-STAT signalling pathways are disrupted in PSEN1 mutant astrocytes. ( A-B ) FACs analysis of cell surface levels of <t>IFNAR2</t> in CD44-positive iPSC-astrocytes, with and without TIC treatment. Data represent 5 experimental repeats from two batches and include 2 control lines and 2 PSEN1 mutant lines. Note that two control lines are pooled for TIC-treated datapoint. Data analysed within treatment subgroups via one-way ANOVA. ( C ) Representative Western blot of iPSC-astrocyte lysates with or without TIC treatment for 24 h. Actin is shown as a loading control. ( D-G ) Western blot analysis of total and phosphorylated MAPK (p42/p44), STAT2, STAT3 and NFκB under basal conditions or after 24 h TIC treatment. Note that one outlier was removed (grey arrow in panel A), due to a z score of 3.47. Data represent up to 4 independent batches and up to 7 technical repeats using 5 controls and 3 PSEN1 mutant lines (see Table ). For data separated by iPSC line, see Fig . ( H-J ) qPCR analysis of ISG15 , OAS1 and CXCL10 ; genes involved in interferon response (associated with JAK-STAT2 signalling). Note that CXCL10 was rarely detectable in untreated conditions (n.d.). Data represent up to 5 independent batches and up to 6 technical repeats from 6 control lines and 3 PSEN1 lines, see Table . For data separated by iPSC line, see Fig . ( K ) High content imaging analysis of nuclear NFκB normalised to cytosolic NFκB and plotted as a fold-change relative to maximum signal. Data represent 2 control lines and 3 PSEN1 lines, with two experimental repeats (see Table ). Individual data presented in Fig . Pairwise comparisons represent two tailed t-tests, where * = p < 0.05, ** = p < 0.01, *** = p < 0.001, and **** = p < 0.0001
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    JAK-STAT signalling pathways are disrupted in PSEN1 mutant astrocytes. ( A-B ) FACs analysis of cell surface levels of <t>IFNAR2</t> in CD44-positive iPSC-astrocytes, with and without TIC treatment. Data represent 5 experimental repeats from two batches and include 2 control lines and 2 PSEN1 mutant lines. Note that two control lines are pooled for TIC-treated datapoint. Data analysed within treatment subgroups via one-way ANOVA. ( C ) Representative Western blot of iPSC-astrocyte lysates with or without TIC treatment for 24 h. Actin is shown as a loading control. ( D-G ) Western blot analysis of total and phosphorylated MAPK (p42/p44), STAT2, STAT3 and NFκB under basal conditions or after 24 h TIC treatment. Note that one outlier was removed (grey arrow in panel A), due to a z score of 3.47. Data represent up to 4 independent batches and up to 7 technical repeats using 5 controls and 3 PSEN1 mutant lines (see Table ). For data separated by iPSC line, see Fig . ( H-J ) qPCR analysis of ISG15 , OAS1 and CXCL10 ; genes involved in interferon response (associated with JAK-STAT2 signalling). Note that CXCL10 was rarely detectable in untreated conditions (n.d.). Data represent up to 5 independent batches and up to 6 technical repeats from 6 control lines and 3 PSEN1 lines, see Table . For data separated by iPSC line, see Fig . ( K ) High content imaging analysis of nuclear NFκB normalised to cytosolic NFκB and plotted as a fold-change relative to maximum signal. Data represent 2 control lines and 3 PSEN1 lines, with two experimental repeats (see Table ). Individual data presented in Fig . Pairwise comparisons represent two tailed t-tests, where * = p < 0.05, ** = p < 0.01, *** = p < 0.001, and **** = p < 0.0001
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    Image Search Results


    JAK-STAT signalling pathways are disrupted in PSEN1 mutant astrocytes. ( A-B ) FACs analysis of cell surface levels of IFNAR2 in CD44-positive iPSC-astrocytes, with and without TIC treatment. Data represent 5 experimental repeats from two batches and include 2 control lines and 2 PSEN1 mutant lines. Note that two control lines are pooled for TIC-treated datapoint. Data analysed within treatment subgroups via one-way ANOVA. ( C ) Representative Western blot of iPSC-astrocyte lysates with or without TIC treatment for 24 h. Actin is shown as a loading control. ( D-G ) Western blot analysis of total and phosphorylated MAPK (p42/p44), STAT2, STAT3 and NFκB under basal conditions or after 24 h TIC treatment. Note that one outlier was removed (grey arrow in panel A), due to a z score of 3.47. Data represent up to 4 independent batches and up to 7 technical repeats using 5 controls and 3 PSEN1 mutant lines (see Table ). For data separated by iPSC line, see Fig . ( H-J ) qPCR analysis of ISG15 , OAS1 and CXCL10 ; genes involved in interferon response (associated with JAK-STAT2 signalling). Note that CXCL10 was rarely detectable in untreated conditions (n.d.). Data represent up to 5 independent batches and up to 6 technical repeats from 6 control lines and 3 PSEN1 lines, see Table . For data separated by iPSC line, see Fig . ( K ) High content imaging analysis of nuclear NFκB normalised to cytosolic NFκB and plotted as a fold-change relative to maximum signal. Data represent 2 control lines and 3 PSEN1 lines, with two experimental repeats (see Table ). Individual data presented in Fig . Pairwise comparisons represent two tailed t-tests, where * = p < 0.05, ** = p < 0.01, *** = p < 0.001, and **** = p < 0.0001

    Journal: Molecular Neurodegeneration

    Article Title: Mutations in PSEN1 predispose inflammation in an astrocyte model of familial Alzheimer’s disease through disrupted regulated intramembrane proteolysis

    doi: 10.1186/s13024-025-00864-7

    Figure Lengend Snippet: JAK-STAT signalling pathways are disrupted in PSEN1 mutant astrocytes. ( A-B ) FACs analysis of cell surface levels of IFNAR2 in CD44-positive iPSC-astrocytes, with and without TIC treatment. Data represent 5 experimental repeats from two batches and include 2 control lines and 2 PSEN1 mutant lines. Note that two control lines are pooled for TIC-treated datapoint. Data analysed within treatment subgroups via one-way ANOVA. ( C ) Representative Western blot of iPSC-astrocyte lysates with or without TIC treatment for 24 h. Actin is shown as a loading control. ( D-G ) Western blot analysis of total and phosphorylated MAPK (p42/p44), STAT2, STAT3 and NFκB under basal conditions or after 24 h TIC treatment. Note that one outlier was removed (grey arrow in panel A), due to a z score of 3.47. Data represent up to 4 independent batches and up to 7 technical repeats using 5 controls and 3 PSEN1 mutant lines (see Table ). For data separated by iPSC line, see Fig . ( H-J ) qPCR analysis of ISG15 , OAS1 and CXCL10 ; genes involved in interferon response (associated with JAK-STAT2 signalling). Note that CXCL10 was rarely detectable in untreated conditions (n.d.). Data represent up to 5 independent batches and up to 6 technical repeats from 6 control lines and 3 PSEN1 lines, see Table . For data separated by iPSC line, see Fig . ( K ) High content imaging analysis of nuclear NFκB normalised to cytosolic NFκB and plotted as a fold-change relative to maximum signal. Data represent 2 control lines and 3 PSEN1 lines, with two experimental repeats (see Table ). Individual data presented in Fig . Pairwise comparisons represent two tailed t-tests, where * = p < 0.05, ** = p < 0.01, *** = p < 0.001, and **** = p < 0.0001

    Article Snippet: IFNAR2-APC , human , Miltenyi Biotec 130-099-560 , RRID: AB_2652223.

    Techniques: Mutagenesis, Control, Western Blot, Imaging, Two Tailed Test