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primary antibodies against hfap  (R&D Systems)


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    R&D Systems primary antibodies against hfap
    Primary Antibodies Against Hfap, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+hfap/Human+Fibroblast+Activation+Protein+alpha%2FFAP+Alexa+Fluor%C2%AE+647-conjugated+Antibody/us11890357-143-0-6
    Average 94 stars, based on 5 article reviews
    primary antibodies against hfap - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Staining:

    Article Title: Differential Marker Expression between Keratinocyte Stem Cells and Their Progeny Generated from a Single Colony
    Article Snippet: For the surface staining, anti-hTHSD1 (R&D systems #FAB3715P), with an appropriately matched isotype control mAb (R&D systems #IC002G), was used. .. The following antibodies were used for intracellular staining: anti-hFAP and anti-hDCBLD2 (R&D systems # FAB3715P, AF6269), with an appropriately matched isotype control mAb (R&D systems # IC002P, 5-001-A). .. The results were assessed using an FACScan (BD Biosciences, San Jose, CA, USA).

    Control:

    Article Title: Differential Marker Expression between Keratinocyte Stem Cells and Their Progeny Generated from a Single Colony
    Article Snippet: For the surface staining, anti-hTHSD1 (R&D systems #FAB3715P), with an appropriately matched isotype control mAb (R&D systems #IC002G), was used. .. The following antibodies were used for intracellular staining: anti-hFAP and anti-hDCBLD2 (R&D systems # FAB3715P, AF6269), with an appropriately matched isotype control mAb (R&D systems # IC002P, 5-001-A). .. The results were assessed using an FACScan (BD Biosciences, San Jose, CA, USA).

    other:

    Article Title: Destabilization of NOXA mRNA as a common resistance mechanism to targeted therapies
    Article Snippet: Antibodies used were: Zombie Aqua Dye (Biolegend, #423101), anti-hFAP (PE conjugated, R&D systems #FAB3715P), CD45 (BD Horizon, BV421clone HI30), and anti-hNG2/MCSP (R&D systems, #FAB2585F, FITC) and cytochrome c-Alexa Fluor 647 (Biolegend, #612310).



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    a , Representative longitudinal PET/CT and CT images of unilateral bleomycin (BLM)-induced pulmonary fibrosis in <t>hFAP-knock-in</t> (hFAP-BLM) mice imaged with 18 F-FAPI and in wild-type C57BL/6-BLM mice imaged with 68 Ga-NOTA-1A12 at days 3, 7, 14, 21, and 28 after modeling. White dashed lines delineate the fibrotic lung regions. b , Quantitative analysis of probe uptake in fibrotic lung regions expressed as SUV mean. Data are presented as mean ± SD ( n = 8∼10 per group). Statistical significance was determined using one-way ANOVA. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, ns: not significant. c , Schematic diagram of the sequential dual-probe PET/CT imaging protocol in the bleomycin-induced pulmonary fibrosis crab-eating macaque model. The macaque was first imaged with 18 F-FAPI on day 4 post-BLM instillation, followed by 68 Ga-NOTA-1A12 imaging on day 6 after sufficient radioactive decay. d , Representative axial, coronal, and maximum intensity projection (MIP) PET/CT images showing lung fibrotic regions with probe accumulation.
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    Image Search Results


    a , Representative longitudinal PET/CT and CT images of unilateral bleomycin (BLM)-induced pulmonary fibrosis in hFAP-knock-in (hFAP-BLM) mice imaged with 18 F-FAPI and in wild-type C57BL/6-BLM mice imaged with 68 Ga-NOTA-1A12 at days 3, 7, 14, 21, and 28 after modeling. White dashed lines delineate the fibrotic lung regions. b , Quantitative analysis of probe uptake in fibrotic lung regions expressed as SUV mean. Data are presented as mean ± SD ( n = 8∼10 per group). Statistical significance was determined using one-way ANOVA. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, ns: not significant. c , Schematic diagram of the sequential dual-probe PET/CT imaging protocol in the bleomycin-induced pulmonary fibrosis crab-eating macaque model. The macaque was first imaged with 18 F-FAPI on day 4 post-BLM instillation, followed by 68 Ga-NOTA-1A12 imaging on day 6 after sufficient radioactive decay. d , Representative axial, coronal, and maximum intensity projection (MIP) PET/CT images showing lung fibrotic regions with probe accumulation.

    Journal: medRxiv

    Article Title: A DDR2-targeted PET tracer images activated fibroblasts in early pulmonary fibrosis

    doi: 10.1101/2025.11.26.25341068

    Figure Lengend Snippet: a , Representative longitudinal PET/CT and CT images of unilateral bleomycin (BLM)-induced pulmonary fibrosis in hFAP-knock-in (hFAP-BLM) mice imaged with 18 F-FAPI and in wild-type C57BL/6-BLM mice imaged with 68 Ga-NOTA-1A12 at days 3, 7, 14, 21, and 28 after modeling. White dashed lines delineate the fibrotic lung regions. b , Quantitative analysis of probe uptake in fibrotic lung regions expressed as SUV mean. Data are presented as mean ± SD ( n = 8∼10 per group). Statistical significance was determined using one-way ANOVA. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, ns: not significant. c , Schematic diagram of the sequential dual-probe PET/CT imaging protocol in the bleomycin-induced pulmonary fibrosis crab-eating macaque model. The macaque was first imaged with 18 F-FAPI on day 4 post-BLM instillation, followed by 68 Ga-NOTA-1A12 imaging on day 6 after sufficient radioactive decay. d , Representative axial, coronal, and maximum intensity projection (MIP) PET/CT images showing lung fibrotic regions with probe accumulation.

    Article Snippet: To generate stable overexpression models, lentiviral vectors carrying human DDR2 or hFAP complementary DNA (IGE Biotechnology, Guangzhou, China) were constructed and co-transfected with packaging plasmids psPAX2 and pMD2.G into 293T cells using Lipofectamine 3000 (Invitrogen).

    Techniques: Positron Emission Tomography-Computed Tomography, Knock-In, Imaging