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ek0468  (Boster Bio)


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    Boster Bio ek0468
    Ek0468, supplied by Boster Bio, used in various techniques. Bioz Stars score: 92/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ek0468/product/Boster Bio
    Average 92 stars, based on 22 article reviews
    ek0468 - by Bioz Stars, 2026-03
    92/100 stars

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    Figure 3. Inflammation inhibition and chondrocyte protection by UCMSCs. (A) Detection of inflammatory factors in synovial fluid. ELISAs were performed to detect IL-1β, TNF-α, and <t>MMP13</t> in synovial fluid. The levels of these three factors decreased significantly in the UCMSC group compared with the model group, indicating that UCMSC transplantation inhibited the expression of key inflammatory factors in OA. Normal, normal group; Model, OA model group; Vehicle, OA model with saline injection; UCMSC, OA model with UCMSC transplantation. n = 6. (B) The effect of UCMSCs on the gene expression levels of aggrecan, Col2, and Sox9 in chondrocytes induced by IL-β1. Chondrocytes co-cultured with UCMSCs and IL-β1 were collected, and RT-PCR was used to detect gene expression levels in chondrocytes. Treatment of chondrocytes with high (1 × 106 cells) and low (0.5 × 106 cells) doses of UCMSCs promoted the expression of aggrecan, Col2, and Sox9 genes. Control, normal cultured rat chondrocytes; Model, rat chondrocytes pre-treated by 10 ng/mL IL-1β; UCMSC-L, rat chondrocytes pre-treated by 10 ng/mL IL-1β were co-cultured with 0.5 × 106 UCMSCs; UCMSC-H, rat chondrocytes pre-treated by10ng/mL IL-1β were co-cultured with 1 × 106 UCMSCs, n = 3. *P < 0.05, **P < 0.01 analyzed by unpaired two-tailed t-test after normality and equal variance test using Shapiro– Wilk test and ANOVA plus Brown–Forsythe test in the GraphPad software.
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    Boster Bio human mmp13 elisa kit
    Figure 3. Inflammation inhibition and chondrocyte protection by UCMSCs. (A) Detection of inflammatory factors in synovial fluid. ELISAs were performed to detect IL-1β, TNF-α, and <t>MMP13</t> in synovial fluid. The levels of these three factors decreased significantly in the UCMSC group compared with the model group, indicating that UCMSC transplantation inhibited the expression of key inflammatory factors in OA. Normal, normal group; Model, OA model group; Vehicle, OA model with saline injection; UCMSC, OA model with UCMSC transplantation. n = 6. (B) The effect of UCMSCs on the gene expression levels of aggrecan, Col2, and Sox9 in chondrocytes induced by IL-β1. Chondrocytes co-cultured with UCMSCs and IL-β1 were collected, and RT-PCR was used to detect gene expression levels in chondrocytes. Treatment of chondrocytes with high (1 × 106 cells) and low (0.5 × 106 cells) doses of UCMSCs promoted the expression of aggrecan, Col2, and Sox9 genes. Control, normal cultured rat chondrocytes; Model, rat chondrocytes pre-treated by 10 ng/mL IL-1β; UCMSC-L, rat chondrocytes pre-treated by 10 ng/mL IL-1β were co-cultured with 0.5 × 106 UCMSCs; UCMSC-H, rat chondrocytes pre-treated by10ng/mL IL-1β were co-cultured with 1 × 106 UCMSCs, n = 3. *P < 0.05, **P < 0.01 analyzed by unpaired two-tailed t-test after normality and equal variance test using Shapiro– Wilk test and ANOVA plus Brown–Forsythe test in the GraphPad software.
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    Figure 3. Inflammation inhibition and chondrocyte protection by UCMSCs. (A) Detection of inflammatory factors in synovial fluid. ELISAs were performed to detect IL-1β, TNF-α, and MMP13 in synovial fluid. The levels of these three factors decreased significantly in the UCMSC group compared with the model group, indicating that UCMSC transplantation inhibited the expression of key inflammatory factors in OA. Normal, normal group; Model, OA model group; Vehicle, OA model with saline injection; UCMSC, OA model with UCMSC transplantation. n = 6. (B) The effect of UCMSCs on the gene expression levels of aggrecan, Col2, and Sox9 in chondrocytes induced by IL-β1. Chondrocytes co-cultured with UCMSCs and IL-β1 were collected, and RT-PCR was used to detect gene expression levels in chondrocytes. Treatment of chondrocytes with high (1 × 106 cells) and low (0.5 × 106 cells) doses of UCMSCs promoted the expression of aggrecan, Col2, and Sox9 genes. Control, normal cultured rat chondrocytes; Model, rat chondrocytes pre-treated by 10 ng/mL IL-1β; UCMSC-L, rat chondrocytes pre-treated by 10 ng/mL IL-1β were co-cultured with 0.5 × 106 UCMSCs; UCMSC-H, rat chondrocytes pre-treated by10ng/mL IL-1β were co-cultured with 1 × 106 UCMSCs, n = 3. *P < 0.05, **P < 0.01 analyzed by unpaired two-tailed t-test after normality and equal variance test using Shapiro– Wilk test and ANOVA plus Brown–Forsythe test in the GraphPad software.

    Journal: Scientific reports

    Article Title: Umbilical cord mesenchymal stem cells relieve osteoarthritis in rats through immunoregulation and inhibition of chondrocyte apoptosis.

    doi: 10.1038/s41598-023-42349-x

    Figure Lengend Snippet: Figure 3. Inflammation inhibition and chondrocyte protection by UCMSCs. (A) Detection of inflammatory factors in synovial fluid. ELISAs were performed to detect IL-1β, TNF-α, and MMP13 in synovial fluid. The levels of these three factors decreased significantly in the UCMSC group compared with the model group, indicating that UCMSC transplantation inhibited the expression of key inflammatory factors in OA. Normal, normal group; Model, OA model group; Vehicle, OA model with saline injection; UCMSC, OA model with UCMSC transplantation. n = 6. (B) The effect of UCMSCs on the gene expression levels of aggrecan, Col2, and Sox9 in chondrocytes induced by IL-β1. Chondrocytes co-cultured with UCMSCs and IL-β1 were collected, and RT-PCR was used to detect gene expression levels in chondrocytes. Treatment of chondrocytes with high (1 × 106 cells) and low (0.5 × 106 cells) doses of UCMSCs promoted the expression of aggrecan, Col2, and Sox9 genes. Control, normal cultured rat chondrocytes; Model, rat chondrocytes pre-treated by 10 ng/mL IL-1β; UCMSC-L, rat chondrocytes pre-treated by 10 ng/mL IL-1β were co-cultured with 0.5 × 106 UCMSCs; UCMSC-H, rat chondrocytes pre-treated by10ng/mL IL-1β were co-cultured with 1 × 106 UCMSCs, n = 3. *P < 0.05, **P < 0.01 analyzed by unpaired two-tailed t-test after normality and equal variance test using Shapiro– Wilk test and ANOVA plus Brown–Forsythe test in the GraphPad software.

    Article Snippet: ELISA kits were used to determine the levels of IL-1β (EK0392, Boster, China), TNF-α (EK0525, Boster), MMP13 (EK0468, Boster), IL-10 (EK0416, Boster), and TGF-β1 (EK0513, Boster) in the supernatant.

    Techniques: Inhibition, Transplantation Assay, Expressing, Saline, Injection, Gene Expression, Cell Culture, Reverse Transcription Polymerase Chain Reaction, Control, Two Tailed Test, Software