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recombinant tgf β2 protein  (MedChemExpress)


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    MedChemExpress recombinant tgf β2 protein
    Recombinant Tgf β2 Protein, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+human+transforming+growth+factor+%CE%B22/Recombinant+Human+Transforming+Growth+Factor+%CE%B22/pmc12670360-59-8-14
    Average 94 stars, based on 9 article reviews
    recombinant tgf β2 protein - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Isolation:

    Article Title: S100B drives glioblastoma invasion and migration through TGF-β2-mediated epithelial-mesenchymal transition
    Article Snippet: , and then the relative percentage rate of positive cells was calculated using NC as the control group. In addition, the shS100B cells were cultured with recombinant TGF-β2 protein (cat. no. HY-P7119; MedChemExpress) for 48 h to obtain shS100B + TGF-β2 cells, which were used for subsequent experimental analyses. Total RNA was isolated from NC and shS100B LN229 GBM cells using AG RNAex Pro Reagent (

    Cell Culture:

    Article Title: S100B drives glioblastoma invasion and migration through TGF-β2-mediated epithelial-mesenchymal transition
    Article Snippet: , and then the relative percentage rate of positive cells was calculated using NC as the control group. In addition, the shS100B cells were cultured with recombinant TGF-β2 protein (cat. no. HY-P7119; MedChemExpress) for 48 h to obtain shS100B + TGF-β2 cells, which were used for subsequent experimental analyses. Total RNA was isolated from NC and shS100B LN229 GBM cells using AG RNAex Pro Reagent (

    Quantitative RT-PCR:

    Article Title: S100B drives glioblastoma invasion and migration through TGF-β2-mediated epithelial-mesenchymal transition
    Article Snippet: , and then the relative percentage rate of positive cells was calculated using NC as the control group. In addition, the shS100B cells were cultured with recombinant TGF-β2 protein (cat. no. HY-P7119; MedChemExpress) for 48 h to obtain shS100B + TGF-β2 cells, which were used for subsequent experimental analyses. Total RNA was isolated from NC and shS100B LN229 GBM cells using AG RNAex Pro Reagent (

    Control:

    Article Title: S100B drives glioblastoma invasion and migration through TGF-β2-mediated epithelial-mesenchymal transition
    Article Snippet: , and then the relative percentage rate of positive cells was calculated using NC as the control group. In addition, the shS100B cells were cultured with recombinant TGF-β2 protein (cat. no. HY-P7119; MedChemExpress) for 48 h to obtain shS100B + TGF-β2 cells, which were used for subsequent experimental analyses. Total RNA was isolated from NC and shS100B LN229 GBM cells using AG RNAex Pro Reagent (

    Recombinant:

    Article Title: S100B drives glioblastoma invasion and migration through TGF-β2-mediated epithelial-mesenchymal transition
    Article Snippet: , and then the relative percentage rate of positive cells was calculated using NC as the control group. In addition, the shS100B cells were cultured with recombinant TGF-β2 protein (cat. no. HY-P7119; MedChemExpress) for 48 h to obtain shS100B + TGF-β2 cells, which were used for subsequent experimental analyses. Total RNA was isolated from NC and shS100B LN229 GBM cells using AG RNAex Pro Reagent (

    Transfection:

    Article Title: S100B drives glioblastoma invasion and migration through TGF-β2-mediated epithelial-mesenchymal transition
    Article Snippet: , and then the relative percentage rate of positive cells was calculated using NC as the control group. In addition, the shS100B cells were cultured with recombinant TGF-β2 protein (cat. no. HY-P7119; MedChemExpress) for 48 h to obtain shS100B + TGF-β2 cells, which were used for subsequent experimental analyses. Total RNA was isolated from NC and shS100B LN229 GBM cells using AG RNAex Pro Reagent (

    Western Blot:

    Article Title: S100B drives glioblastoma invasion and migration through TGF-β2-mediated epithelial-mesenchymal transition
    Article Snippet: , and then the relative percentage rate of positive cells was calculated using NC as the control group. In addition, the shS100B cells were cultured with recombinant TGF-β2 protein (cat. no. HY-P7119; MedChemExpress) for 48 h to obtain shS100B + TGF-β2 cells, which were used for subsequent experimental analyses. Total RNA was isolated from NC and shS100B LN229 GBM cells using AG RNAex Pro Reagent (

    Expressing:

    Article Title: S100B drives glioblastoma invasion and migration through TGF-β2-mediated epithelial-mesenchymal transition
    Article Snippet: , and then the relative percentage rate of positive cells was calculated using NC as the control group. In addition, the shS100B cells were cultured with recombinant TGF-β2 protein (cat. no. HY-P7119; MedChemExpress) for 48 h to obtain shS100B + TGF-β2 cells, which were used for subsequent experimental analyses. Total RNA was isolated from NC and shS100B LN229 GBM cells using AG RNAex Pro Reagent (



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    tgf β activity  (MedChemExpress)
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    Gdf11 forms heterodimer with Spaw and regulates DFC specification <t>through</t> <t>TGF‐β</t> signal. (A) Immunoprecipitation between zGdf11‐Flag and zSpaw‐Myc in HEK 293T cells. (B) Western blot results of overexpressed zGdf11‐Flag and zSpaw‐Myc in HEK 293T cells with or without SB431542 treatment. (C) foxj1a and its target gene expression using WISH in WT or gdf11 mutants with or without treatment. (D–G) Expression levels of foxj1a and its target genes. Error bars represent the standard deviation. Statistical significance was determined using a two‐tailed unpaired t ‐test. (H) Visualization of KV cilia at the 10‐somite stage using an anti‐acetylated tubulin antibody in both WT or gdf11 −/− mutants with or without SB431542/SRI‐011381 treatment. Scale bar, 50 μm. (I, J) Number (I) and length (J) of KV cilia in WT and mutant embryos with or without SB431542/SRI‐011381 treatment. Graph indicates the mean of cilia number and length, error bars represent the standard deviation.
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    Image Search Results


    Gdf11 forms heterodimer with Spaw and regulates DFC specification through TGF‐β signal. (A) Immunoprecipitation between zGdf11‐Flag and zSpaw‐Myc in HEK 293T cells. (B) Western blot results of overexpressed zGdf11‐Flag and zSpaw‐Myc in HEK 293T cells with or without SB431542 treatment. (C) foxj1a and its target gene expression using WISH in WT or gdf11 mutants with or without treatment. (D–G) Expression levels of foxj1a and its target genes. Error bars represent the standard deviation. Statistical significance was determined using a two‐tailed unpaired t ‐test. (H) Visualization of KV cilia at the 10‐somite stage using an anti‐acetylated tubulin antibody in both WT or gdf11 −/− mutants with or without SB431542/SRI‐011381 treatment. Scale bar, 50 μm. (I, J) Number (I) and length (J) of KV cilia in WT and mutant embryos with or without SB431542/SRI‐011381 treatment. Graph indicates the mean of cilia number and length, error bars represent the standard deviation.

    Journal: Cell Proliferation

    Article Title: Gdf11 regulates left‐right asymmetry development through TGF ‐β signal

    doi: 10.1111/cpr.13765

    Figure Lengend Snippet: Gdf11 forms heterodimer with Spaw and regulates DFC specification through TGF‐β signal. (A) Immunoprecipitation between zGdf11‐Flag and zSpaw‐Myc in HEK 293T cells. (B) Western blot results of overexpressed zGdf11‐Flag and zSpaw‐Myc in HEK 293T cells with or without SB431542 treatment. (C) foxj1a and its target gene expression using WISH in WT or gdf11 mutants with or without treatment. (D–G) Expression levels of foxj1a and its target genes. Error bars represent the standard deviation. Statistical significance was determined using a two‐tailed unpaired t ‐test. (H) Visualization of KV cilia at the 10‐somite stage using an anti‐acetylated tubulin antibody in both WT or gdf11 −/− mutants with or without SB431542/SRI‐011381 treatment. Scale bar, 50 μm. (I, J) Number (I) and length (J) of KV cilia in WT and mutant embryos with or without SB431542/SRI‐011381 treatment. Graph indicates the mean of cilia number and length, error bars represent the standard deviation.

    Article Snippet: For activating TGF‐β activity, mutant embryos were treated with 0.2 μM SRI‐011381 (HY‐100347, MedChemExpress) from the shield stage to the 75% epiboly or 10 ss.

    Techniques: Immunoprecipitation, Western Blot, Targeted Gene Expression, Expressing, Standard Deviation, Two Tailed Test, Mutagenesis