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antibody ib4-488 thermo fisher cat#: i21411  (Thermo Fisher)


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    Thermo Fisher antibody ib4-488 thermo fisher cat#: i21411
    Antibody Ib4 488 Thermo Fisher Cat#: I21411, supplied by Thermo Fisher, 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/result/antibody ib4-488 thermo fisher cat#: i21411/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    antibody ib4-488 thermo fisher cat#: i21411 - by Bioz Stars, 2026-05
    90/100 stars

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    Fig. 2 Db/db mice + 1% salt show microvascular dysfunction before the onset of diastolic dysfunction. (A, B) Cardiac capillary density measured as the number of <t>IB4</t> + microvessels per area in db/+ and db/db + 1% salt mice at 2, 4, 6 and 8 weeks with representative images (n = 5–8/group). (C) Number of pericytes was determined by counting the cells that were double positive for NG2 and PDGFRb marker, and co-localised with IB4 + microvessels. (D) Pericyte coverage, assessed by the ratio of IB4 + microvessels covered by NG2/PDGFRb double positive cells over total IB4 + microvessels. (E, F) Active vessel regression, assessed by the ratio of Coll IV + IB4- microvessels over total IB4 + microvessels with representative images at 4 and 6 weeks (n = 5–8/ group). White arrowheads indicate empty collagen sleeves. Scalebars are 6 μm. Values are presented as mean ± SEM. Two-way ANOVA followed by Sidak’s multiple comparisons test with *p < 0.05, **p < 0.01, and ***p < 0.001. IB4, isolectin B4; NG2, neural glial antigen 2; NS, non-significant; PDGFRb, platelet derived growth factor receptor beta; Coll IV, collagen IV. At 2 weeks: n = 8 F (1 db/+, 7 db/db) and 5 M (4db/+, 1 db/db); at 4 weeks: n = 7 F (4 db/+, 3 db/ db) and 8 M (4 db/+, 4db/db); at 6 weeks: n = 7 F (3 db/+, 4 db/db) and 6 M (3 db/+, 3 db/db), at 8 weeks: 4 F (2 db/+, 2db/db) and 6 M (3 db/+, 3 db/db)
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    Fig. 2 Db/db mice + 1% salt show microvascular dysfunction before the onset of diastolic dysfunction. (A, B) Cardiac capillary density measured as the number of <t>IB4</t> + microvessels per area in db/+ and db/db + 1% salt mice at 2, 4, 6 and 8 weeks with representative images (n = 5–8/group). (C) Number of pericytes was determined by counting the cells that were double positive for NG2 and PDGFRb marker, and co-localised with IB4 + microvessels. (D) Pericyte coverage, assessed by the ratio of IB4 + microvessels covered by NG2/PDGFRb double positive cells over total IB4 + microvessels. (E, F) Active vessel regression, assessed by the ratio of Coll IV + IB4- microvessels over total IB4 + microvessels with representative images at 4 and 6 weeks (n = 5–8/ group). White arrowheads indicate empty collagen sleeves. Scalebars are 6 μm. Values are presented as mean ± SEM. Two-way ANOVA followed by Sidak’s multiple comparisons test with *p < 0.05, **p < 0.01, and ***p < 0.001. IB4, isolectin B4; NG2, neural glial antigen 2; NS, non-significant; PDGFRb, platelet derived growth factor receptor beta; Coll IV, collagen IV. At 2 weeks: n = 8 F (1 db/+, 7 db/db) and 5 M (4db/+, 1 db/db); at 4 weeks: n = 7 F (4 db/+, 3 db/ db) and 8 M (4 db/+, 4db/db); at 6 weeks: n = 7 F (3 db/+, 4 db/db) and 6 M (3 db/+, 3 db/db), at 8 weeks: 4 F (2 db/+, 2db/db) and 6 M (3 db/+, 3 db/db)
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    Thermo Fisher isolectin gs-ib 4 -488 ib4 antibody
    Fig. 2 Db/db mice + 1% salt show microvascular dysfunction before the onset of diastolic dysfunction. (A, B) Cardiac capillary density measured as the number of <t>IB4</t> + microvessels per area in db/+ and db/db + 1% salt mice at 2, 4, 6 and 8 weeks with representative images (n = 5–8/group). (C) Number of pericytes was determined by counting the cells that were double positive for NG2 and PDGFRb marker, and co-localised with IB4 + microvessels. (D) Pericyte coverage, assessed by the ratio of IB4 + microvessels covered by NG2/PDGFRb double positive cells over total IB4 + microvessels. (E, F) Active vessel regression, assessed by the ratio of Coll IV + IB4- microvessels over total IB4 + microvessels with representative images at 4 and 6 weeks (n = 5–8/ group). White arrowheads indicate empty collagen sleeves. Scalebars are 6 μm. Values are presented as mean ± SEM. Two-way ANOVA followed by Sidak’s multiple comparisons test with *p < 0.05, **p < 0.01, and ***p < 0.001. IB4, isolectin B4; NG2, neural glial antigen 2; NS, non-significant; PDGFRb, platelet derived growth factor receptor beta; Coll IV, collagen IV. At 2 weeks: n = 8 F (1 db/+, 7 db/db) and 5 M (4db/+, 1 db/db); at 4 weeks: n = 7 F (4 db/+, 3 db/ db) and 8 M (4 db/+, 4db/db); at 6 weeks: n = 7 F (3 db/+, 4 db/db) and 6 M (3 db/+, 3 db/db), at 8 weeks: 4 F (2 db/+, 2db/db) and 6 M (3 db/+, 3 db/db)
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    Fig. 2 Db/db mice + 1% salt show microvascular dysfunction before the onset of diastolic dysfunction. (A, B) Cardiac capillary density measured as the number of <t>IB4</t> + microvessels per area in db/+ and db/db + 1% salt mice at 2, 4, 6 and 8 weeks with representative images (n = 5–8/group). (C) Number of pericytes was determined by counting the cells that were double positive for NG2 and PDGFRb marker, and co-localised with IB4 + microvessels. (D) Pericyte coverage, assessed by the ratio of IB4 + microvessels covered by NG2/PDGFRb double positive cells over total IB4 + microvessels. (E, F) Active vessel regression, assessed by the ratio of Coll IV + IB4- microvessels over total IB4 + microvessels with representative images at 4 and 6 weeks (n = 5–8/ group). White arrowheads indicate empty collagen sleeves. Scalebars are 6 μm. Values are presented as mean ± SEM. Two-way ANOVA followed by Sidak’s multiple comparisons test with *p < 0.05, **p < 0.01, and ***p < 0.001. IB4, isolectin B4; NG2, neural glial antigen 2; NS, non-significant; PDGFRb, platelet derived growth factor receptor beta; Coll IV, collagen IV. At 2 weeks: n = 8 F (1 db/+, 7 db/db) and 5 M (4db/+, 1 db/db); at 4 weeks: n = 7 F (4 db/+, 3 db/ db) and 8 M (4 db/+, 4db/db); at 6 weeks: n = 7 F (3 db/+, 4 db/db) and 6 M (3 db/+, 3 db/db), at 8 weeks: 4 F (2 db/+, 2db/db) and 6 M (3 db/+, 3 db/db)
    Fitc Conjugated Ib4 L2895 Antibody, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Fig. 2 Db/db mice + 1% salt show microvascular dysfunction before the onset of diastolic dysfunction. (A, B) Cardiac capillary density measured as the number of IB4 + microvessels per area in db/+ and db/db + 1% salt mice at 2, 4, 6 and 8 weeks with representative images (n = 5–8/group). (C) Number of pericytes was determined by counting the cells that were double positive for NG2 and PDGFRb marker, and co-localised with IB4 + microvessels. (D) Pericyte coverage, assessed by the ratio of IB4 + microvessels covered by NG2/PDGFRb double positive cells over total IB4 + microvessels. (E, F) Active vessel regression, assessed by the ratio of Coll IV + IB4- microvessels over total IB4 + microvessels with representative images at 4 and 6 weeks (n = 5–8/ group). White arrowheads indicate empty collagen sleeves. Scalebars are 6 μm. Values are presented as mean ± SEM. Two-way ANOVA followed by Sidak’s multiple comparisons test with *p < 0.05, **p < 0.01, and ***p < 0.001. IB4, isolectin B4; NG2, neural glial antigen 2; NS, non-significant; PDGFRb, platelet derived growth factor receptor beta; Coll IV, collagen IV. At 2 weeks: n = 8 F (1 db/+, 7 db/db) and 5 M (4db/+, 1 db/db); at 4 weeks: n = 7 F (4 db/+, 3 db/ db) and 8 M (4 db/+, 4db/db); at 6 weeks: n = 7 F (3 db/+, 4 db/db) and 6 M (3 db/+, 3 db/db), at 8 weeks: 4 F (2 db/+, 2db/db) and 6 M (3 db/+, 3 db/db)

    Journal: Cardiovascular diabetology

    Article Title: Mural cell dysfunction contributes to diastolic heart failure by promoting endothelial dysfunction and vessel remodelling.

    doi: 10.1186/s12933-025-02623-w

    Figure Lengend Snippet: Fig. 2 Db/db mice + 1% salt show microvascular dysfunction before the onset of diastolic dysfunction. (A, B) Cardiac capillary density measured as the number of IB4 + microvessels per area in db/+ and db/db + 1% salt mice at 2, 4, 6 and 8 weeks with representative images (n = 5–8/group). (C) Number of pericytes was determined by counting the cells that were double positive for NG2 and PDGFRb marker, and co-localised with IB4 + microvessels. (D) Pericyte coverage, assessed by the ratio of IB4 + microvessels covered by NG2/PDGFRb double positive cells over total IB4 + microvessels. (E, F) Active vessel regression, assessed by the ratio of Coll IV + IB4- microvessels over total IB4 + microvessels with representative images at 4 and 6 weeks (n = 5–8/ group). White arrowheads indicate empty collagen sleeves. Scalebars are 6 μm. Values are presented as mean ± SEM. Two-way ANOVA followed by Sidak’s multiple comparisons test with *p < 0.05, **p < 0.01, and ***p < 0.001. IB4, isolectin B4; NG2, neural glial antigen 2; NS, non-significant; PDGFRb, platelet derived growth factor receptor beta; Coll IV, collagen IV. At 2 weeks: n = 8 F (1 db/+, 7 db/db) and 5 M (4db/+, 1 db/db); at 4 weeks: n = 7 F (4 db/+, 3 db/ db) and 8 M (4 db/+, 4db/db); at 6 weeks: n = 7 F (3 db/+, 4 db/db) and 6 M (3 db/+, 3 db/db), at 8 weeks: 4 F (2 db/+, 2db/db) and 6 M (3 db/+, 3 db/db)

    Article Snippet: Paraffin sections were stained with IB4 and rabbit anti-p21 antibody (Novus, NB100-1941, 1/50).

    Techniques: Marker, Derivative Assay