Review




Structured Review

Proteintech tgf β2
Tgf β2, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 78 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/tgf β2/product/Proteintech
Average 95 stars, based on 78 article reviews
tgf β2 - by Bioz Stars, 2026-03
95/100 stars

Images



Similar Products

95
Proteintech tgf β2
Tgf β2, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/tgf β2/product/Proteintech
Average 95 stars, based on 1 article reviews
tgf β2 - by Bioz Stars, 2026-03
95/100 stars
  Buy from Supplier

95
Proteintech anti tgf β2 rabbit polyclonal antibody
Fig. 3 PRMT1 inhibition increases the expression of MMP-10, PlGF and <t>TGF-β2</t> in ADSCs. (A) Volcano plot comparing changes in genes with up-regulated or down-regulated expression in ADSCs treated with vehicle or Furamidine (10 µM) for 24 h (n = 3). (B) GO (Gene ontology) was used to analyze the bubble map of differential gene-enriched molecules in ADSCs. (C) Heat map of mRNA expression profile of ADSCs treated with vehicle or Furamidine. (D) ADSCs treated with Furamidine (10 µM, 24 h) showed changes in mRNA expression levels of target genes (n = 6). (E) The mRNA expression levels of target genes in ADSCs infected with Ad-control or Ad-shPRMT1 (MOI 200, 24 h) (n = 6). (F, G) Western blotting and protein quantitative analysis showed the protein changes of target genes after ADSCs were infected with adenovirus for 48 h (n = 6). Full-length blots are presented in Supplementary Fig. 4D. Data are presented as mean ± SEM and were analyzed using student’s t test, *P < 0.05
Anti Tgf β2 Rabbit Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti tgf β2 rabbit polyclonal antibody/product/Proteintech
Average 95 stars, based on 1 article reviews
anti tgf β2 rabbit polyclonal antibody - by Bioz Stars, 2026-03
95/100 stars
  Buy from Supplier

90
Thermo Fisher rabbit anti-tgf-β2
Fig. 3 PRMT1 inhibition increases the expression of MMP-10, PlGF and <t>TGF-β2</t> in ADSCs. (A) Volcano plot comparing changes in genes with up-regulated or down-regulated expression in ADSCs treated with vehicle or Furamidine (10 µM) for 24 h (n = 3). (B) GO (Gene ontology) was used to analyze the bubble map of differential gene-enriched molecules in ADSCs. (C) Heat map of mRNA expression profile of ADSCs treated with vehicle or Furamidine. (D) ADSCs treated with Furamidine (10 µM, 24 h) showed changes in mRNA expression levels of target genes (n = 6). (E) The mRNA expression levels of target genes in ADSCs infected with Ad-control or Ad-shPRMT1 (MOI 200, 24 h) (n = 6). (F, G) Western blotting and protein quantitative analysis showed the protein changes of target genes after ADSCs were infected with adenovirus for 48 h (n = 6). Full-length blots are presented in Supplementary Fig. 4D. Data are presented as mean ± SEM and were analyzed using student’s t test, *P < 0.05
Rabbit Anti Tgf β2, 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/rabbit anti-tgf-β2/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
rabbit anti-tgf-β2 - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

95
Proteintech anti tgf β2
Fig. 3 PRMT1 inhibition increases the expression of MMP-10, PlGF and <t>TGF-β2</t> in ADSCs. (A) Volcano plot comparing changes in genes with up-regulated or down-regulated expression in ADSCs treated with vehicle or Furamidine (10 µM) for 24 h (n = 3). (B) GO (Gene ontology) was used to analyze the bubble map of differential gene-enriched molecules in ADSCs. (C) Heat map of mRNA expression profile of ADSCs treated with vehicle or Furamidine. (D) ADSCs treated with Furamidine (10 µM, 24 h) showed changes in mRNA expression levels of target genes (n = 6). (E) The mRNA expression levels of target genes in ADSCs infected with Ad-control or Ad-shPRMT1 (MOI 200, 24 h) (n = 6). (F, G) Western blotting and protein quantitative analysis showed the protein changes of target genes after ADSCs were infected with adenovirus for 48 h (n = 6). Full-length blots are presented in Supplementary Fig. 4D. Data are presented as mean ± SEM and were analyzed using student’s t test, *P < 0.05
Anti Tgf β2, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti tgf β2/product/Proteintech
Average 95 stars, based on 1 article reviews
anti tgf β2 - by Bioz Stars, 2026-03
95/100 stars
  Buy from Supplier

Image Search Results


Fig. 3 PRMT1 inhibition increases the expression of MMP-10, PlGF and TGF-β2 in ADSCs. (A) Volcano plot comparing changes in genes with up-regulated or down-regulated expression in ADSCs treated with vehicle or Furamidine (10 µM) for 24 h (n = 3). (B) GO (Gene ontology) was used to analyze the bubble map of differential gene-enriched molecules in ADSCs. (C) Heat map of mRNA expression profile of ADSCs treated with vehicle or Furamidine. (D) ADSCs treated with Furamidine (10 µM, 24 h) showed changes in mRNA expression levels of target genes (n = 6). (E) The mRNA expression levels of target genes in ADSCs infected with Ad-control or Ad-shPRMT1 (MOI 200, 24 h) (n = 6). (F, G) Western blotting and protein quantitative analysis showed the protein changes of target genes after ADSCs were infected with adenovirus for 48 h (n = 6). Full-length blots are presented in Supplementary Fig. 4D. Data are presented as mean ± SEM and were analyzed using student’s t test, *P < 0.05

Journal: Stem cell research & therapy

Article Title: PRMT1 inhibition enhances the cardioprotective effect of adipose-derived mesenchymal stem cells against myocardial infarction through RUNX1.

doi: 10.1186/s13287-025-04409-z

Figure Lengend Snippet: Fig. 3 PRMT1 inhibition increases the expression of MMP-10, PlGF and TGF-β2 in ADSCs. (A) Volcano plot comparing changes in genes with up-regulated or down-regulated expression in ADSCs treated with vehicle or Furamidine (10 µM) for 24 h (n = 3). (B) GO (Gene ontology) was used to analyze the bubble map of differential gene-enriched molecules in ADSCs. (C) Heat map of mRNA expression profile of ADSCs treated with vehicle or Furamidine. (D) ADSCs treated with Furamidine (10 µM, 24 h) showed changes in mRNA expression levels of target genes (n = 6). (E) The mRNA expression levels of target genes in ADSCs infected with Ad-control or Ad-shPRMT1 (MOI 200, 24 h) (n = 6). (F, G) Western blotting and protein quantitative analysis showed the protein changes of target genes after ADSCs were infected with adenovirus for 48 h (n = 6). Full-length blots are presented in Supplementary Fig. 4D. Data are presented as mean ± SEM and were analyzed using student’s t test, *P < 0.05

Article Snippet: The primary antibodies used in this study included: anti-PRMT1 rabbit monoclonal antibody (2449 S, 1:1000; Cell Signaling Technology, MA, USA), anti-cleaved caspase-3 rabbit polyclonal antibody (9664 S, 1:1000; Cell Signaling Technology, MA, USA), anti-MMP-10 rabbit polyclonal antibody (A3033, 1:1000; Abclonal Technology, Wuhan, China), anti-TGF-β2 rabbit polyclonal antibody (19999-1-AP, 1:1000; Proteintech, Wuhan, China), anti-PlGF rabbit polyclonal antibody (10642-1-AP, 1:1000; Proteintech, Wuhan, China), anti-RUNX1 rabbit polyclonal antibody (25315-1-AP, 1:1000; Proteintech, Wuhan, China), anti-GAPDH rabbit polyclonal antibody (10494-1-AP, 1:10000; Proteintech, Wuhan, China).

Techniques: Inhibition, Expressing, Infection, Control, Western Blot

Fig. 4 PRMT1 inhibition promotes proliferation and migration of ADSCs through RUNX1-mediated MMP-10/PlGF/TGF-β2 expression in ADSCs. (A) Pre dicted transcription factors binding to the target Mmp10, Plgf and Tgfb2 genes promoter region. The promoter region is defined as 2000 bp upstream of the target gene transcription starting point. (B) Predict possible binding sites in the gene promoter region and transcription factor RUNX1. (C, D) The relationship between PRMT1 and RUNX1 was detected by Co-IP experiment. (E, F) ADSCs were treated with Furamidine (10 µM) and Ro5-3335 (50 µM) for 48 h. Full-length blots are presented in Supplementary Fig. 4E, F. Western blotting and quantitative analysis of MMP-10, PlGF, and TGF-β2 protein levels (n = 6). Full-length blots are presented in Supplementary Fig. 5A. (G) Changes in cell proliferation were detected by CCK-8 after ADSCs were treated with Furamidine and Ro5-3335 for 24 h (n = 6). (H, I) Representative images of crystal violet staining. The migration ability of ADSCs was observed by transwell assay after treatment with Furamidine and Ro5-3335 (n = 4). Scale bar: 50 μm. All data are presented as mean ± SEM and were analyzed by one-way ANOVA, *P < 0.05

Journal: Stem cell research & therapy

Article Title: PRMT1 inhibition enhances the cardioprotective effect of adipose-derived mesenchymal stem cells against myocardial infarction through RUNX1.

doi: 10.1186/s13287-025-04409-z

Figure Lengend Snippet: Fig. 4 PRMT1 inhibition promotes proliferation and migration of ADSCs through RUNX1-mediated MMP-10/PlGF/TGF-β2 expression in ADSCs. (A) Pre dicted transcription factors binding to the target Mmp10, Plgf and Tgfb2 genes promoter region. The promoter region is defined as 2000 bp upstream of the target gene transcription starting point. (B) Predict possible binding sites in the gene promoter region and transcription factor RUNX1. (C, D) The relationship between PRMT1 and RUNX1 was detected by Co-IP experiment. (E, F) ADSCs were treated with Furamidine (10 µM) and Ro5-3335 (50 µM) for 48 h. Full-length blots are presented in Supplementary Fig. 4E, F. Western blotting and quantitative analysis of MMP-10, PlGF, and TGF-β2 protein levels (n = 6). Full-length blots are presented in Supplementary Fig. 5A. (G) Changes in cell proliferation were detected by CCK-8 after ADSCs were treated with Furamidine and Ro5-3335 for 24 h (n = 6). (H, I) Representative images of crystal violet staining. The migration ability of ADSCs was observed by transwell assay after treatment with Furamidine and Ro5-3335 (n = 4). Scale bar: 50 μm. All data are presented as mean ± SEM and were analyzed by one-way ANOVA, *P < 0.05

Article Snippet: The primary antibodies used in this study included: anti-PRMT1 rabbit monoclonal antibody (2449 S, 1:1000; Cell Signaling Technology, MA, USA), anti-cleaved caspase-3 rabbit polyclonal antibody (9664 S, 1:1000; Cell Signaling Technology, MA, USA), anti-MMP-10 rabbit polyclonal antibody (A3033, 1:1000; Abclonal Technology, Wuhan, China), anti-TGF-β2 rabbit polyclonal antibody (19999-1-AP, 1:1000; Proteintech, Wuhan, China), anti-PlGF rabbit polyclonal antibody (10642-1-AP, 1:1000; Proteintech, Wuhan, China), anti-RUNX1 rabbit polyclonal antibody (25315-1-AP, 1:1000; Proteintech, Wuhan, China), anti-GAPDH rabbit polyclonal antibody (10494-1-AP, 1:10000; Proteintech, Wuhan, China).

Techniques: Inhibition, Migration, Expressing, Binding Assay, Co-Immunoprecipitation Assay, Western Blot, CCK-8 Assay, Staining, Transwell Assay