7666 mb Search Results


97
R&D Systems tgf β1
Tgf β1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/7666+mb/pmc08985356-151-21-24?v=R%26D+Systems
Average 97 stars, based on 1 article reviews
tgf β1 - by Bioz Stars, 2026-08
97/100 stars
  Buy from Supplier

96
R&D Systems recombinant mouse tgf β protein
CD206 M2‐like macrophages differentiate in the absence STAT6 but retain proinflammatory properties (A) Immunofluorescent labeling of CD206, CCR2 and CD3 in CP tissue. (B) Quantification of CD206 + , CCR2 + and CD3 + cells in the pancreas of CP mice ( n = 10). (C) Heat map illustrating different levels of inflammation related proteins between wild type and Stat6‐/‐ mice. The numbers in the boxes represents the change compared with untreated control mice, the amount of all red labeled proteins were significantly changed in Stat6‐/‐ compared to wild type mice after onset of CP ( n = 5). (D) Quantitative gene expression analysis by RT‐qPCR of Arg1 , Fizz , Ym1 and Il10 in CP tissue of wild type and Stat6‐/‐ mice ( n = 5). (E) Immunofluorescent labeling of MMP9 (red) and α‐amylase (green) in CP tissue and quantification of MMP9 + cells in the pancreas of CP mice. (F) Quantitative RT‐PCR of Nos2 , Il1b , Mmp9 and Il6 in CP tissue of wild type and Stat6‐/‐ mice ( n = 10). (G) Measurement <t>of</t> <t>TGF‐β</t> in serum of untreated control mice and CP mice ( n = 9). (H) Quantitative RT‐PCR of Tgfbi and Csf1 in CP tissue of wild type and Stat6‐/‐ mice ( n = 5). Data in B and D‐H are shown as mean +/‐ SEM. Differences were tested for statistical significance by unpaired students t‐test or Mann–Whitney for non‐normally distributed samples for independent samples, significance levels of p < 0.05 are marked by an asterisk.
Recombinant Mouse Tgf β Protein, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/7666+mb/pmc12970205-282-28-33?v=R%26D+Systems
Average 96 stars, based on 1 article reviews
recombinant mouse tgf β protein - by Bioz Stars, 2026-08
96/100 stars
  Buy from Supplier

94
R&D Systems tgfβ
CD206 M2‐like macrophages differentiate in the absence STAT6 but retain proinflammatory properties (A) Immunofluorescent labeling of CD206, CCR2 and CD3 in CP tissue. (B) Quantification of CD206 + , CCR2 + and CD3 + cells in the pancreas of CP mice ( n = 10). (C) Heat map illustrating different levels of inflammation related proteins between wild type and Stat6‐/‐ mice. The numbers in the boxes represents the change compared with untreated control mice, the amount of all red labeled proteins were significantly changed in Stat6‐/‐ compared to wild type mice after onset of CP ( n = 5). (D) Quantitative gene expression analysis by RT‐qPCR of Arg1 , Fizz , Ym1 and Il10 in CP tissue of wild type and Stat6‐/‐ mice ( n = 5). (E) Immunofluorescent labeling of MMP9 (red) and α‐amylase (green) in CP tissue and quantification of MMP9 + cells in the pancreas of CP mice. (F) Quantitative RT‐PCR of Nos2 , Il1b , Mmp9 and Il6 in CP tissue of wild type and Stat6‐/‐ mice ( n = 10). (G) Measurement <t>of</t> <t>TGF‐β</t> in serum of untreated control mice and CP mice ( n = 9). (H) Quantitative RT‐PCR of Tgfbi and Csf1 in CP tissue of wild type and Stat6‐/‐ mice ( n = 5). Data in B and D‐H are shown as mean +/‐ SEM. Differences were tested for statistical significance by unpaired students t‐test or Mann–Whitney for non‐normally distributed samples for independent samples, significance levels of p < 0.05 are marked by an asterisk.
Tgfβ, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/7666+mb/pmc06992796-360-27-29?v=R%26D+Systems
Average 94 stars, based on 1 article reviews
tgfβ - by Bioz Stars, 2026-08
94/100 stars
  Buy from Supplier

93
R&D Systems recombinant mouse tgfβ1
a , Heatmap visualizing the average expression of conserved receptor-ligand pairs identified as significant interactions in human SLOs by CellPhoneDB analysis. b , c , Fold changes of SOX9 ( b ) and PI16 ( c ) mRNA levels in bulk cultured primary tonsillar fibroblast of OSA patients stimulated with the indicated recombinant proteins for 48 h and measured by qRT-PCR. d , Fold changes of PI16 mRNA levels after in vitro expansion of sorted PI16 + RCs from human tonsils and following stimulation with TGF-β1 for 48 h. b – d , Box plots with whiskers showing the minimum and maximum values. Horizontal lines indicate the median and boxes represent 0.25−0.75 percentiles ( b , c ) q values are derived from Tukey’s test following Kruskal-Wallis test and using Benjamini, Krieger and Yekutieli correction to control the false discovery rate. ( d ) Two-sided Mann Whitney test was used to test for significant differences. In a , data represent 3,450 CXCL13 + cells and 56,887 immune cells sampled from n = 4 patients for human lymph nodes and n = 4 patients for human palatine tonsils. In b , c , cells from n = 8 patients were cultivated and processed in 2 independent experiments. In d , cells from n = 5 patients were cultivated and processed in 2 independent experiments.
Recombinant Mouse Tgfβ1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/7666+mb/pmc10307622-218-23-34?v=R%26D+Systems
Average 93 stars, based on 1 article reviews
recombinant mouse tgfβ1 - by Bioz Stars, 2026-08
93/100 stars
  Buy from Supplier

Image Search Results


CD206 M2‐like macrophages differentiate in the absence STAT6 but retain proinflammatory properties (A) Immunofluorescent labeling of CD206, CCR2 and CD3 in CP tissue. (B) Quantification of CD206 + , CCR2 + and CD3 + cells in the pancreas of CP mice ( n = 10). (C) Heat map illustrating different levels of inflammation related proteins between wild type and Stat6‐/‐ mice. The numbers in the boxes represents the change compared with untreated control mice, the amount of all red labeled proteins were significantly changed in Stat6‐/‐ compared to wild type mice after onset of CP ( n = 5). (D) Quantitative gene expression analysis by RT‐qPCR of Arg1 , Fizz , Ym1 and Il10 in CP tissue of wild type and Stat6‐/‐ mice ( n = 5). (E) Immunofluorescent labeling of MMP9 (red) and α‐amylase (green) in CP tissue and quantification of MMP9 + cells in the pancreas of CP mice. (F) Quantitative RT‐PCR of Nos2 , Il1b , Mmp9 and Il6 in CP tissue of wild type and Stat6‐/‐ mice ( n = 10). (G) Measurement of TGF‐β in serum of untreated control mice and CP mice ( n = 9). (H) Quantitative RT‐PCR of Tgfbi and Csf1 in CP tissue of wild type and Stat6‐/‐ mice ( n = 5). Data in B and D‐H are shown as mean +/‐ SEM. Differences were tested for statistical significance by unpaired students t‐test or Mann–Whitney for non‐normally distributed samples for independent samples, significance levels of p < 0.05 are marked by an asterisk.

Journal: Advanced Science

Article Title: IL‐4/STAT6‐signaling Influences Local Inflammation and Regeneration Processes During Acute Pancreatitis and Promotes Fibrosis by a Direct Activation of Pancreatic Fibroblasts During Chronic Pancreatitis

doi: 10.1002/advs.202515585

Figure Lengend Snippet: CD206 M2‐like macrophages differentiate in the absence STAT6 but retain proinflammatory properties (A) Immunofluorescent labeling of CD206, CCR2 and CD3 in CP tissue. (B) Quantification of CD206 + , CCR2 + and CD3 + cells in the pancreas of CP mice ( n = 10). (C) Heat map illustrating different levels of inflammation related proteins between wild type and Stat6‐/‐ mice. The numbers in the boxes represents the change compared with untreated control mice, the amount of all red labeled proteins were significantly changed in Stat6‐/‐ compared to wild type mice after onset of CP ( n = 5). (D) Quantitative gene expression analysis by RT‐qPCR of Arg1 , Fizz , Ym1 and Il10 in CP tissue of wild type and Stat6‐/‐ mice ( n = 5). (E) Immunofluorescent labeling of MMP9 (red) and α‐amylase (green) in CP tissue and quantification of MMP9 + cells in the pancreas of CP mice. (F) Quantitative RT‐PCR of Nos2 , Il1b , Mmp9 and Il6 in CP tissue of wild type and Stat6‐/‐ mice ( n = 10). (G) Measurement of TGF‐β in serum of untreated control mice and CP mice ( n = 9). (H) Quantitative RT‐PCR of Tgfbi and Csf1 in CP tissue of wild type and Stat6‐/‐ mice ( n = 5). Data in B and D‐H are shown as mean +/‐ SEM. Differences were tested for statistical significance by unpaired students t‐test or Mann–Whitney for non‐normally distributed samples for independent samples, significance levels of p < 0.05 are marked by an asterisk.

Article Snippet: Recombinant Mouse IL‐4 Protein (#404‐ML, R&D Systems), Recombinant Mouse IL‐13 Protein (#413‐ML, R&D Systems), Lipopolysaccharide Escherichia coli O26:B6 (L8274, Sigma Aldrich), Recombinant Mouse IL‐6 Protein (406‐ML, R&D systems), Recombinant Mouse TGF‐β Protein (7666‐MB, R&D systems), Recombinant mouse IL‐10 (575804, BioLegend).

Techniques: Labeling, Control, Gene Expression, Quantitative RT-PCR, MANN-WHITNEY

a , Heatmap visualizing the average expression of conserved receptor-ligand pairs identified as significant interactions in human SLOs by CellPhoneDB analysis. b , c , Fold changes of SOX9 ( b ) and PI16 ( c ) mRNA levels in bulk cultured primary tonsillar fibroblast of OSA patients stimulated with the indicated recombinant proteins for 48 h and measured by qRT-PCR. d , Fold changes of PI16 mRNA levels after in vitro expansion of sorted PI16 + RCs from human tonsils and following stimulation with TGF-β1 for 48 h. b – d , Box plots with whiskers showing the minimum and maximum values. Horizontal lines indicate the median and boxes represent 0.25−0.75 percentiles ( b , c ) q values are derived from Tukey’s test following Kruskal-Wallis test and using Benjamini, Krieger and Yekutieli correction to control the false discovery rate. ( d ) Two-sided Mann Whitney test was used to test for significant differences. In a , data represent 3,450 CXCL13 + cells and 56,887 immune cells sampled from n = 4 patients for human lymph nodes and n = 4 patients for human palatine tonsils. In b , c , cells from n = 8 patients were cultivated and processed in 2 independent experiments. In d , cells from n = 5 patients were cultivated and processed in 2 independent experiments.

Journal: Nature Immunology

Article Title: Conserved stromal–immune cell circuits secure B cell homeostasis and function

doi: 10.1038/s41590-023-01503-3

Figure Lengend Snippet: a , Heatmap visualizing the average expression of conserved receptor-ligand pairs identified as significant interactions in human SLOs by CellPhoneDB analysis. b , c , Fold changes of SOX9 ( b ) and PI16 ( c ) mRNA levels in bulk cultured primary tonsillar fibroblast of OSA patients stimulated with the indicated recombinant proteins for 48 h and measured by qRT-PCR. d , Fold changes of PI16 mRNA levels after in vitro expansion of sorted PI16 + RCs from human tonsils and following stimulation with TGF-β1 for 48 h. b – d , Box plots with whiskers showing the minimum and maximum values. Horizontal lines indicate the median and boxes represent 0.25−0.75 percentiles ( b , c ) q values are derived from Tukey’s test following Kruskal-Wallis test and using Benjamini, Krieger and Yekutieli correction to control the false discovery rate. ( d ) Two-sided Mann Whitney test was used to test for significant differences. In a , data represent 3,450 CXCL13 + cells and 56,887 immune cells sampled from n = 4 patients for human lymph nodes and n = 4 patients for human palatine tonsils. In b , c , cells from n = 8 patients were cultivated and processed in 2 independent experiments. In d , cells from n = 5 patients were cultivated and processed in 2 independent experiments.

Article Snippet: To evaluate the differentiation and activation potential, 1.5 × 10 4 cells were plated in 24-well plates and stimulated for 48 h with recombinant mouse TGFβ1 (10 ng ml −1 , catalog no. 7666-MB/CF, R&D Systems), recombinant mouse PRGN (10 ng ml −1 , catalog no. 2557-PG, R&D Systems), recombinant mouse VEGF (25 ng ml −1 , catalog no. 493-MV/CF, R&D Systems), recombinant mouse IL-4 (10 ng ml −1 , catalog no. 404-ML/CF, R&D Systems) or recombinant mouse IL-1β (1 ng ml −1 , catalog no. ab259421, Abcam).

Techniques: Expressing, Cell Culture, Recombinant, Quantitative RT-PCR, In Vitro, Derivative Assay, Control, MANN-WHITNEY