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rabbit anti fap α primary antibody  (Bioss)


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    Bioss rabbit anti fap α primary antibody
    Rabbit Anti Fap α Primary Antibody, supplied by Bioss, 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/result/rabbit anti fap α primary antibody/product/Bioss
    Average 94 stars, based on 22 article reviews
    rabbit anti fap α primary antibody - by Bioz Stars, 2026-02
    94/100 stars

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    Fig. 2 CSF2 regulates the pro-tumor phenotype and function of MSCs. A In vitro tropism of MSCs towards HGC-27 cells assessed via a transwell system. Original magnification: ×100. Scale bar = 50 μm. B qRT-PCR analysis of FAP and α-SMA expression in MSCs and P-MSCs. C Western blot analyses of FAP and α-SMA expression in MSCs and P-MSCs. D Luminex assay to determine the inflammatory cytokine profile in the supernatants from MSCs and P-MSCs. E Cell viability assay for HGC-27 cells treated with the supernatants from MSCs and P-MSCs. F Colony formation assays for HGC-27 cells treated with the supernatants from MSCs and P-MSCs. G Transwell migration assay for HGC-27 cells treated with the supernatants from MSCs and P-MSCs. Original magnification: ×100. Scale bar = 50 μm. H CCK-8 assay for IC50 of 5-FU in HGC-27 cells treated with the supernatants from MSCs and P-MSCs. I Flow cytometry analyses of the apoptotic rate of HGC-27 cells exposed to 5-FU. *P < 0.05; **P < 0.01; ***P < 0.001.

    Journal: Cell death & disease

    Article Title: IGF2BP2-meidated m 6 A modification of CSF2 reprograms MSC to promote gastric cancer progression.

    doi: 10.1038/s41419-023-06163-7

    Figure Lengend Snippet: Fig. 2 CSF2 regulates the pro-tumor phenotype and function of MSCs. A In vitro tropism of MSCs towards HGC-27 cells assessed via a transwell system. Original magnification: ×100. Scale bar = 50 μm. B qRT-PCR analysis of FAP and α-SMA expression in MSCs and P-MSCs. C Western blot analyses of FAP and α-SMA expression in MSCs and P-MSCs. D Luminex assay to determine the inflammatory cytokine profile in the supernatants from MSCs and P-MSCs. E Cell viability assay for HGC-27 cells treated with the supernatants from MSCs and P-MSCs. F Colony formation assays for HGC-27 cells treated with the supernatants from MSCs and P-MSCs. G Transwell migration assay for HGC-27 cells treated with the supernatants from MSCs and P-MSCs. Original magnification: ×100. Scale bar = 50 μm. H CCK-8 assay for IC50 of 5-FU in HGC-27 cells treated with the supernatants from MSCs and P-MSCs. I Flow cytometry analyses of the apoptotic rate of HGC-27 cells exposed to 5-FU. *P < 0.05; **P < 0.01; ***P < 0.001.

    Article Snippet: Primary antibodies against FAP (#66562), α-SMA (#19245), Notch1 (#3608), CSF2 (#56712), ubiquitin (#20326) (Cell Signaling Technology, USA), and IGF2BP2 (11601-1-AP, Proteintech, Wuhan, China) were applied to the membranes for incubation. β-actin (CW0096M, Cwbio, Beijing, China) was used as the loading control.

    Techniques: In Vitro, Quantitative RT-PCR, Expressing, Western Blot, Luminex, Viability Assay, Transwell Migration Assay, CCK-8 Assay, Flow Cytometry

    Fig. 4 IGF2BP2 modulates CSF2 m6A modification to induce MSC reprogramming. A In vitro tropism of MSCs towards HGC-27 cells assessed via a transwell system. Original magnification: ×100. Scale bar = 50 μm. B, C qRT-PCR (B) and western blot (C) analyses of FAP and α- SMA expression in MSCs from different groups. D Luminex analyses of the inflammatory factor profile in the supernatants from MSCs. E, F The proliferation of HGC-27 cells following exposure to the supernatants from different MSCs was assessed by cell viability (E) and colony formation assays (F). G Transwell assay for the migration of HGC-27 cells upon treatment with the supernatants from different MSCs. Original magnification: ×100. Scale bar = 50 μm. H CCK-8 assay for IC50 of 5-FU in HGC-27 cells treated with the supernatants from different MSCs. I Flow cytometric analyses of the apoptotic rate of HGC-27 cells after exposure to 5-FU. *P < 0.05; **P < 0.01; ***P < 0.001.

    Journal: Cell death & disease

    Article Title: IGF2BP2-meidated m 6 A modification of CSF2 reprograms MSC to promote gastric cancer progression.

    doi: 10.1038/s41419-023-06163-7

    Figure Lengend Snippet: Fig. 4 IGF2BP2 modulates CSF2 m6A modification to induce MSC reprogramming. A In vitro tropism of MSCs towards HGC-27 cells assessed via a transwell system. Original magnification: ×100. Scale bar = 50 μm. B, C qRT-PCR (B) and western blot (C) analyses of FAP and α- SMA expression in MSCs from different groups. D Luminex analyses of the inflammatory factor profile in the supernatants from MSCs. E, F The proliferation of HGC-27 cells following exposure to the supernatants from different MSCs was assessed by cell viability (E) and colony formation assays (F). G Transwell assay for the migration of HGC-27 cells upon treatment with the supernatants from different MSCs. Original magnification: ×100. Scale bar = 50 μm. H CCK-8 assay for IC50 of 5-FU in HGC-27 cells treated with the supernatants from different MSCs. I Flow cytometric analyses of the apoptotic rate of HGC-27 cells after exposure to 5-FU. *P < 0.05; **P < 0.01; ***P < 0.001.

    Article Snippet: Primary antibodies against FAP (#66562), α-SMA (#19245), Notch1 (#3608), CSF2 (#56712), ubiquitin (#20326) (Cell Signaling Technology, USA), and IGF2BP2 (11601-1-AP, Proteintech, Wuhan, China) were applied to the membranes for incubation. β-actin (CW0096M, Cwbio, Beijing, China) was used as the loading control.

    Techniques: In Vitro, Quantitative RT-PCR, Western Blot, Expressing, Luminex, Transwell Assay, Migration, CCK-8 Assay

    Fig. 6 IGF2BP2/CSF2/Notch1 axis regulates MSC reprogramming. A In vitro tropism of MSCs towards HGC-27 cells assessed via a transwell system. Original magnification: ×100. Scale bar = 50 μm. B, C qRT-PCR (B) and western blot (C) were performed to analyze the expression of FAP and α-SMA in different MSCs. D Luminex assay was employed to examine the inflammatory factor profile in MSC supernatant from each group. E, F Cell viability assays (E) and colony formation assays (F) were performed to assess the proliferation of HGC-27 cells treated with the supernatants from different MSCs. G Transwell assays were performed to evaluate the migration of HGC-27 cells treated with MSC supernatant from each group. Original magnification: ×100. Scale bar = 50 μm. H CCK-8 assay for IC50 of 5-FU in HGC-27 cells. *P < 0.05; **P < 0.01; ***P < 0.001.

    Journal: Cell death & disease

    Article Title: IGF2BP2-meidated m 6 A modification of CSF2 reprograms MSC to promote gastric cancer progression.

    doi: 10.1038/s41419-023-06163-7

    Figure Lengend Snippet: Fig. 6 IGF2BP2/CSF2/Notch1 axis regulates MSC reprogramming. A In vitro tropism of MSCs towards HGC-27 cells assessed via a transwell system. Original magnification: ×100. Scale bar = 50 μm. B, C qRT-PCR (B) and western blot (C) were performed to analyze the expression of FAP and α-SMA in different MSCs. D Luminex assay was employed to examine the inflammatory factor profile in MSC supernatant from each group. E, F Cell viability assays (E) and colony formation assays (F) were performed to assess the proliferation of HGC-27 cells treated with the supernatants from different MSCs. G Transwell assays were performed to evaluate the migration of HGC-27 cells treated with MSC supernatant from each group. Original magnification: ×100. Scale bar = 50 μm. H CCK-8 assay for IC50 of 5-FU in HGC-27 cells. *P < 0.05; **P < 0.01; ***P < 0.001.

    Article Snippet: Primary antibodies against FAP (#66562), α-SMA (#19245), Notch1 (#3608), CSF2 (#56712), ubiquitin (#20326) (Cell Signaling Technology, USA), and IGF2BP2 (11601-1-AP, Proteintech, Wuhan, China) were applied to the membranes for incubation. β-actin (CW0096M, Cwbio, Beijing, China) was used as the loading control.

    Techniques: In Vitro, Quantitative RT-PCR, Western Blot, Expressing, Luminex, Migration, CCK-8 Assay