synoviocyte growth medium (Cell Applications Inc)
Structured Review

Synoviocyte Growth Medium, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 94/100, based on 23 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/synoviocyte+growth+medium/bio_rxiv__64898__2026__04__03__716316-186-7-10?v=Cell+Applications+Inc
Average 94 stars, based on 23 article reviews
Images
1) Product Images from "A human synovial tendon-on-a-chip models key features of peritendinous adhesions and offers a new approach methodology for testing anti-fibrotic drugs"
Article Title: A human synovial tendon-on-a-chip models key features of peritendinous adhesions and offers a new approach methodology for testing anti-fibrotic drugs
Journal: bioRxiv
doi: 10.64898/2026.04.03.716316
Figure Legend Snippet: a , Immunofluorescence images of HUVEC cultured in monolayer and stained for VE-cadherin (green) and Hoechst (blue) compare four different media conditions at 24 h and 72 h of culture. b, Mean fluorescence intensity (MFI) of VE-cadherin expression at b, 24 h and c, 72 h, normalized to MFI of EGM-2 images. Synoviocyte growth media had significantly less VE-cadherin expression at 24 h compared to EGM-2. VE-cadherin MFI for 1:1 Synoviocyte Growth Media:EGM-2 most closely matched that of EGM-2 conditions. d, Immunofluorescence images of FLS cultured in a monolayer, stained for cadherin-11 (yellow) and Hoechst (blue) compare the four different media conditions at 24 h and 72 h of culture. e, MFI quantification of cadherin-11 expression, normalized to MFI of Synoviocyte Growth Media, demonstrated no significant differences between culture conditions at 24 h. f, At 72 h, EGM-2 and 1:1 Synoviocyte Growth Media:EGM-2 had significantly higher cadherin-11 expression compared to Synoviocyte Growth Media, while DMEM had comparable levels. One-way ANOVA with Tukey’s post-hoc test: n=3 wells per condition, *p<0.05, **p<0.01, ***p<0.001.
Techniques Used: Immunofluorescence, Cell Culture, Staining, Fluorescence, Expressing