human tgf ������2 picokine elisa kit Search Results


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    • human bmp2 elisa kit  (Boster Bio)
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    Boster Bio human bmp2 elisa kit
    Primary antibodies used in immunohistochemical studies.
    Human Bmp2 Elisa Kit, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    vegf elisa kit  (Boster Bio)
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    Boster Bio vegf elisa kit
    Primary antibodies used in immunohistochemical studies.
    Vegf Elisa Kit, supplied by Boster Bio, 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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    mmp2 elisa kit  (Boster Bio)
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    P85α deletion converts fibroblasts into activated myofibroblasts exhibiting features of CAFs. ( a ) Western blot analysis of p85α, phospho-Akt, Akt and α-smooth muscle actin (α-SMA) expression in WT and p85α −/− fibroblasts. p-Akt, Phospho-Akt (Ser473); T-Akt, Akt (pan). ( b ) Immunofluorescence analysis of α-SMA expression in WT and p85α −/− fibroblasts. Scale bar, 50μm. ( c ) The area of the contracted gels induced by WT or p85α −/− fibroblasts. The appearance of the contracted gels that have four replications at 72 h is also shown. ( d ) The morphology of WT or p85α −/− fibroblasts in a dish or collagen lattice described in ( c ). ( e ) Immunofluorescence, western blot and fluorescence-activated cell sorting (FACS) analysis of CD44 expression in WT and p85α −/− fibroblasts. Scale bar, 20 μm. ( f ) Reverse transcription–PCR analysis of TGF-β family proteins and SDF-1. <t>MMP2</t> and MMP9 expression in WT and p85α −/− fibroblasts. ( g ) Quantitative PCR analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in WT and p85α −/− fibroblasts. Data are the mean±s.e.m. ( h ) Enzyme-linked immunosorbent assay <t>(ELISA)</t> analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in conditioned medium of WT and p85α −/− fibroblasts. Data are the mean±s.e.m. ** P- value⩽0.01. ( i ) ELISA analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in p85α −/− fibroblast-conditioned medium of when treated with or without the PI3K inhibitor LY294002 (50 μ M ) for 24 h and the DMSO solution as a control. Con, p85α −/− fibroblasts treated with DMSO, LY, p85α −/− fibroblasts treated with LY294002. Data are the mean±s.e.m. ** P- value⩽0.01.
    Mmp2 Elisa Kit, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    lipocalin ngal elisa assay kits  (Boster Bio)
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    P85α deletion converts fibroblasts into activated myofibroblasts exhibiting features of CAFs. ( a ) Western blot analysis of p85α, phospho-Akt, Akt and α-smooth muscle actin (α-SMA) expression in WT and p85α −/− fibroblasts. p-Akt, Phospho-Akt (Ser473); T-Akt, Akt (pan). ( b ) Immunofluorescence analysis of α-SMA expression in WT and p85α −/− fibroblasts. Scale bar, 50μm. ( c ) The area of the contracted gels induced by WT or p85α −/− fibroblasts. The appearance of the contracted gels that have four replications at 72 h is also shown. ( d ) The morphology of WT or p85α −/− fibroblasts in a dish or collagen lattice described in ( c ). ( e ) Immunofluorescence, western blot and fluorescence-activated cell sorting (FACS) analysis of CD44 expression in WT and p85α −/− fibroblasts. Scale bar, 20 μm. ( f ) Reverse transcription–PCR analysis of TGF-β family proteins and SDF-1. <t>MMP2</t> and MMP9 expression in WT and p85α −/− fibroblasts. ( g ) Quantitative PCR analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in WT and p85α −/− fibroblasts. Data are the mean±s.e.m. ( h ) Enzyme-linked immunosorbent assay <t>(ELISA)</t> analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in conditioned medium of WT and p85α −/− fibroblasts. Data are the mean±s.e.m. ** P- value⩽0.01. ( i ) ELISA analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in p85α −/− fibroblast-conditioned medium of when treated with or without the PI3K inhibitor LY294002 (50 μ M ) for 24 h and the DMSO solution as a control. Con, p85α −/− fibroblasts treated with DMSO, LY, p85α −/− fibroblasts treated with LY294002. Data are the mean±s.e.m. ** P- value⩽0.01.
    Lipocalin Ngal Elisa Assay Kits, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    human timp 2 elisa kit  (Boster Bio)
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    Boster Bio human timp 2 elisa kit
    P85α deletion converts fibroblasts into activated myofibroblasts exhibiting features of CAFs. ( a ) Western blot analysis of p85α, phospho-Akt, Akt and α-smooth muscle actin (α-SMA) expression in WT and p85α −/− fibroblasts. p-Akt, Phospho-Akt (Ser473); T-Akt, Akt (pan). ( b ) Immunofluorescence analysis of α-SMA expression in WT and p85α −/− fibroblasts. Scale bar, 50μm. ( c ) The area of the contracted gels induced by WT or p85α −/− fibroblasts. The appearance of the contracted gels that have four replications at 72 h is also shown. ( d ) The morphology of WT or p85α −/− fibroblasts in a dish or collagen lattice described in ( c ). ( e ) Immunofluorescence, western blot and fluorescence-activated cell sorting (FACS) analysis of CD44 expression in WT and p85α −/− fibroblasts. Scale bar, 20 μm. ( f ) Reverse transcription–PCR analysis of TGF-β family proteins and SDF-1. <t>MMP2</t> and MMP9 expression in WT and p85α −/− fibroblasts. ( g ) Quantitative PCR analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in WT and p85α −/− fibroblasts. Data are the mean±s.e.m. ( h ) Enzyme-linked immunosorbent assay <t>(ELISA)</t> analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in conditioned medium of WT and p85α −/− fibroblasts. Data are the mean±s.e.m. ** P- value⩽0.01. ( i ) ELISA analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in p85α −/− fibroblast-conditioned medium of when treated with or without the PI3K inhibitor LY294002 (50 μ M ) for 24 h and the DMSO solution as a control. Con, p85α −/− fibroblasts treated with DMSO, LY, p85α −/− fibroblasts treated with LY294002. Data are the mean±s.e.m. ** P- value⩽0.01.
    Human Timp 2 Elisa Kit, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Primary antibodies used in immunohistochemical studies.

    Journal: Turkish Journal of Biology

    Article Title: The promising effects of BMP2 transfected mesenchymal stem cells on human osteosarcoma

    doi: 10.3906/biy-2101-50

    Figure Lengend Snippet: Primary antibodies used in immunohistochemical studies.

    Article Snippet: The BMP2 levels in hMSCs and BMP2 + hMSCs cultures, and 143B+hMSCs and 143B+BMP2 + hMSCs cocultures were measured (×3 for each sample) in the 4th and 14th culture days using human BMP2 ELISA kit (#EK0311, Boster, Pleasanton, CA, USA) according to the manufacturer’s instructions.

    Techniques: Immunohistochemical staining

    Primer sequences used in RT-PCR.

    Journal: Turkish Journal of Biology

    Article Title: The promising effects of BMP2 transfected mesenchymal stem cells on human osteosarcoma

    doi: 10.3906/biy-2101-50

    Figure Lengend Snippet: Primer sequences used in RT-PCR.

    Article Snippet: The BMP2 levels in hMSCs and BMP2 + hMSCs cultures, and 143B+hMSCs and 143B+BMP2 + hMSCs cocultures were measured (×3 for each sample) in the 4th and 14th culture days using human BMP2 ELISA kit (#EK0311, Boster, Pleasanton, CA, USA) according to the manufacturer’s instructions.

    Techniques:

    P85α deletion converts fibroblasts into activated myofibroblasts exhibiting features of CAFs. ( a ) Western blot analysis of p85α, phospho-Akt, Akt and α-smooth muscle actin (α-SMA) expression in WT and p85α −/− fibroblasts. p-Akt, Phospho-Akt (Ser473); T-Akt, Akt (pan). ( b ) Immunofluorescence analysis of α-SMA expression in WT and p85α −/− fibroblasts. Scale bar, 50μm. ( c ) The area of the contracted gels induced by WT or p85α −/− fibroblasts. The appearance of the contracted gels that have four replications at 72 h is also shown. ( d ) The morphology of WT or p85α −/− fibroblasts in a dish or collagen lattice described in ( c ). ( e ) Immunofluorescence, western blot and fluorescence-activated cell sorting (FACS) analysis of CD44 expression in WT and p85α −/− fibroblasts. Scale bar, 20 μm. ( f ) Reverse transcription–PCR analysis of TGF-β family proteins and SDF-1. MMP2 and MMP9 expression in WT and p85α −/− fibroblasts. ( g ) Quantitative PCR analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in WT and p85α −/− fibroblasts. Data are the mean±s.e.m. ( h ) Enzyme-linked immunosorbent assay (ELISA) analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in conditioned medium of WT and p85α −/− fibroblasts. Data are the mean±s.e.m. ** P- value⩽0.01. ( i ) ELISA analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in p85α −/− fibroblast-conditioned medium of when treated with or without the PI3K inhibitor LY294002 (50 μ M ) for 24 h and the DMSO solution as a control. Con, p85α −/− fibroblasts treated with DMSO, LY, p85α −/− fibroblasts treated with LY294002. Data are the mean±s.e.m. ** P- value⩽0.01.

    Journal: Oncogene

    Article Title: Aberrant low expression of p85α in stromal fibroblasts promotes breast cancer cell metastasis through exosome-mediated paracrine Wnt10b

    doi: 10.1038/onc.2017.100

    Figure Lengend Snippet: P85α deletion converts fibroblasts into activated myofibroblasts exhibiting features of CAFs. ( a ) Western blot analysis of p85α, phospho-Akt, Akt and α-smooth muscle actin (α-SMA) expression in WT and p85α −/− fibroblasts. p-Akt, Phospho-Akt (Ser473); T-Akt, Akt (pan). ( b ) Immunofluorescence analysis of α-SMA expression in WT and p85α −/− fibroblasts. Scale bar, 50μm. ( c ) The area of the contracted gels induced by WT or p85α −/− fibroblasts. The appearance of the contracted gels that have four replications at 72 h is also shown. ( d ) The morphology of WT or p85α −/− fibroblasts in a dish or collagen lattice described in ( c ). ( e ) Immunofluorescence, western blot and fluorescence-activated cell sorting (FACS) analysis of CD44 expression in WT and p85α −/− fibroblasts. Scale bar, 20 μm. ( f ) Reverse transcription–PCR analysis of TGF-β family proteins and SDF-1. MMP2 and MMP9 expression in WT and p85α −/− fibroblasts. ( g ) Quantitative PCR analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in WT and p85α −/− fibroblasts. Data are the mean±s.e.m. ( h ) Enzyme-linked immunosorbent assay (ELISA) analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in conditioned medium of WT and p85α −/− fibroblasts. Data are the mean±s.e.m. ** P- value⩽0.01. ( i ) ELISA analysis of TGF-β1, SDF-1, MMP2 and MMP9 expression in p85α −/− fibroblast-conditioned medium of when treated with or without the PI3K inhibitor LY294002 (50 μ M ) for 24 h and the DMSO solution as a control. Con, p85α −/− fibroblasts treated with DMSO, LY, p85α −/− fibroblasts treated with LY294002. Data are the mean±s.e.m. ** P- value⩽0.01.

    Article Snippet: The supernatants were measured using a commercially available SDF-1 ELISA Kit (R&D Systems, Minneapolis, MN, USA), a TGF-β1 ELISA Kit (Boster Bio-Tech, Wuhan, China), an MMP2 ELISA Kit (Boster Bio-Tech), an MMP9 ELISA Kit (Boster Bio-Tech) and a Wnt10b ELISA Kit (Cusabio Biotech, Wuhan, China).

    Techniques: Western Blot, Expressing, Immunofluorescence, Fluorescence, FACS, Real-time Polymerase Chain Reaction, Enzyme-linked Immunosorbent Assay