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synoviocyte growth medium  (Cell Applications Inc)


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    Structured Review

    Cell Applications Inc synoviocyte growth medium
    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. <t>Synoviocyte</t> 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.
    Synoviocyte Growth Medium, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 94/100, based on 16 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+synoviocyte+growth+medium/Human+Synoviocyte+Media/bio_rxiv__64898__2026__04__03__716316-186-7-10
    Average 94 stars, based on 16 article reviews
    synoviocyte growth medium - by Bioz Stars, 2026-10
    94/100 stars

    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

    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.
    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

    Related Articles

    other:

    Article Title: Targeting protein-protein interaction for immunomodulation: A sunflower trypsin inhibitor analog peptidomimetic suppresses RA progression in CIA model.
    Article Snippet: Human fibroblastlike synoviocytes rheumatoid arthritis (HFLS-RA) cells were purchased from Cell Applications, Inc., San Diego, CA, USA, and maintained in a human synoviocyte growth medium purchased from Cell Applications, Inc. All cell lines were maintained at 37 C and 5% CO2.

    Article Title: Targeting protein–protein interaction for immunomodulation: A sunflower trypsin inhibitor analog peptidomimetic suppresses RA progression in CIA model
    Article Snippet: Human fibroblast-like synoviocytes rheumatoid arthritis (HFLS-RA) cells were purchased from Cell Applications, Inc., San Diego, CA, USA, and maintained in a human synoviocyte growth medium purchased from Cell Applications, Inc. All cell lines were maintained at 37 °C and 5% CO 2 .

    Expressing:

    Article Title: Modulation of co-stimulatory signal from CD2-CD58 proteins by a grafted peptide.
    Article Snippet: Jurkat cells were cultured in RPMI-1640 medium (ATCC) with 10% FBS, 0.01 mg/mL bovine insulin and 0.1 mg/mL penicillin/streptomycin. .. Human fibroblast-like synoviocytes rheumatoid arthritis (HFLS-RA) cells were purchased from Cell Applications, Inc., San Diego, CA, USA, and maintained in human synoviocyte growth medium purchased from Cell Applications, Inc. OVCAR-3 cells and HFLS-RA cells were used as a model for cells expressing CD58 protein, and Jurkat cells were used as a model for human T cells. .. 2.2 Chemicals Fmoc-protected amino acids, piperidine, trifluoroacetic acid (TFA), 2-chlorotrityl chloride resin, 2 - (6 - chloro - 1H - benzotriazole - 1 - yl) - 1,1,3,3 - tetramethylaminium hexafluorophosphate (HCTU), and 1, 1-[bis(dimethylamino) methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluorophosphate (HATU) were purchased from Advanced ChemTech (Louisville, KY).



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    Image Search Results


    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.

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    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

    doi: 10.64898/2026.04.03.716316

    Figure Lengend 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.

    Article Snippet: FLS were expanded in T-75 flasks in Synoviocyte Growth Medium (Cell Applications, 415K-500).

    Techniques: Immunofluorescence, Cell Culture, Staining, Fluorescence, Expressing