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rat elisa kits  (Elabscience Biotechnology)


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    Structured Review

    Elabscience Biotechnology rat elisa kits
    Rat Elisa Kits, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 280 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rat elisa kits/product/Elabscience Biotechnology
    Average 96 stars, based on 280 article reviews
    rat elisa kits - by Bioz Stars, 2026-06
    96/100 stars

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    Figure 2: Shows the mucosal content of <t>PGE2</t> in the control, INDO-administered, and, DAPA-pretreated groups,
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    AVI inhibits the degradation of OA cartilage extracellular matrix and suppresses inflammatory responses. (A) The impact of various concentrations of AVI on rat chondrocyte viability. (B) The effect of different concentrations of AVI on IL-1ẞ-induced rat chondrocytes. (C) Immunofluorescence for Collagen II. (D) Immunofluorescence for MMP13. (E–G) Western blot and quantitative analysis for Collagen II and MMP13 expression levels. (H, I) qRT-PCR analysis for Collagen II and MMP13 gene expression. (J–L) <t>ELISA</t> results for IL-6, TNF-α, and <t>PGE2</t> levels. All data are represented as mean ± SD (n = 3). Compared with the blank group.#p < 0.05,# #p < 0.01,# # #p < 0.001, # # # #p < 0.0001; compared with the OA model group, “p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.
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    AVI inhibits the degradation of OA cartilage extracellular matrix and suppresses inflammatory responses. (A) The impact of various concentrations of AVI on rat chondrocyte viability. (B) The effect of different concentrations of AVI on IL-1ẞ-induced rat chondrocytes. (C) Immunofluorescence for Collagen II. (D) Immunofluorescence for MMP13. (E–G) Western blot and quantitative analysis for Collagen II and MMP13 expression levels. (H, I) qRT-PCR analysis for Collagen II and MMP13 gene expression. (J–L) <t>ELISA</t> results for IL-6, TNF-α, and <t>PGE2</t> levels. All data are represented as mean ± SD (n = 3). Compared with the blank group.#p < 0.05,# #p < 0.01,# # #p < 0.001, # # # #p < 0.0001; compared with the OA model group, “p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.
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    Elabscience Biotechnology rat pge2
    AVI inhibits the degradation of OA cartilage extracellular matrix and suppresses inflammatory responses. (A) The impact of various concentrations of AVI on rat chondrocyte viability. (B) The effect of different concentrations of AVI on IL-1ẞ-induced rat chondrocytes. (C) Immunofluorescence for Collagen II. (D) Immunofluorescence for MMP13. (E–G) Western blot and quantitative analysis for Collagen II and MMP13 expression levels. (H, I) qRT-PCR analysis for Collagen II and MMP13 gene expression. (J–L) <t>ELISA</t> results for IL-6, TNF-α, and <t>PGE2</t> levels. All data are represented as mean ± SD (n = 3). Compared with the blank group.#p < 0.05,# #p < 0.01,# # #p < 0.001, # # # #p < 0.0001; compared with the OA model group, “p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.
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    Image Search Results


    Figure 2: Shows the mucosal content of PGE2 in the control, INDO-administered, and, DAPA-pretreated groups,

    Journal: ERU Research Journal

    Article Title: The gastroprotective effects of dapagliflozin against NSAID-induced ulcerated rats

    doi: 10.21608/erurj.2025.272088.1127

    Figure Lengend Snippet: Figure 2: Shows the mucosal content of PGE2 in the control, INDO-administered, and, DAPA-pretreated groups,

    Article Snippet: Rat PGE2 kit (cat#: CSB-E07967r; CUSABIO, TX, USA) was used.

    Techniques: Control

    AVI inhibits the degradation of OA cartilage extracellular matrix and suppresses inflammatory responses. (A) The impact of various concentrations of AVI on rat chondrocyte viability. (B) The effect of different concentrations of AVI on IL-1ẞ-induced rat chondrocytes. (C) Immunofluorescence for Collagen II. (D) Immunofluorescence for MMP13. (E–G) Western blot and quantitative analysis for Collagen II and MMP13 expression levels. (H, I) qRT-PCR analysis for Collagen II and MMP13 gene expression. (J–L) ELISA results for IL-6, TNF-α, and PGE2 levels. All data are represented as mean ± SD (n = 3). Compared with the blank group.#p < 0.05,# #p < 0.01,# # #p < 0.001, # # # #p < 0.0001; compared with the OA model group, “p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.

    Journal: Frontiers in Pharmacology

    Article Title: Asperosaponin VI suppresses ferroptosis in chondrocytes and ameliorates osteoarthritis by modulating the Nrf2/GPX4/HO-1 signaling pathway

    doi: 10.3389/fphar.2025.1539092

    Figure Lengend Snippet: AVI inhibits the degradation of OA cartilage extracellular matrix and suppresses inflammatory responses. (A) The impact of various concentrations of AVI on rat chondrocyte viability. (B) The effect of different concentrations of AVI on IL-1ẞ-induced rat chondrocytes. (C) Immunofluorescence for Collagen II. (D) Immunofluorescence for MMP13. (E–G) Western blot and quantitative analysis for Collagen II and MMP13 expression levels. (H, I) qRT-PCR analysis for Collagen II and MMP13 gene expression. (J–L) ELISA results for IL-6, TNF-α, and PGE2 levels. All data are represented as mean ± SD (n = 3). Compared with the blank group.#p < 0.05,# #p < 0.01,# # #p < 0.001, # # # #p < 0.0001; compared with the OA model group, “p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.

    Article Snippet: The following ELISA kits were used: Rat TNF-α High Sensitivity ELISA Kit (EK382HS-96, MultiSciences, China), Rat IL-6 ELISA Kit (JYM0646Ra, Wuhan Jiyinmei Biotech, China),and Rat Prostaglandin E2 (PGE2) ELISA Kit (JYM0446Ra, Wuhan Jiyinmei Biotech, China).The levels of Fe 2+ and MDA in the cells post-intervention were determined using the Cell Ferrous Iron Colorimetric Assay Kit (E-BC-K881-M, Elabscience, China) and the MDA Colorimetric Assay Kit for Cell Samples (E-BCK0, Elabscience, China).

    Techniques: Immunofluorescence, Western Blot, Expressing, Quantitative RT-PCR, Gene Expression, Enzyme-linked Immunosorbent Assay

    AVI suppresses ferroptosis and confers protection to OA cartilage. (A) Fe 2+ content in each group. (B) MDA content in each group. (C–E) Western blot and quantitative analysis of GPX4 and ACSL4 expression levels. (F–G) qRT-PCR analysis of GPX4 and ACSL4 gene expression. (H–L) Western blot and quantitative analysis for Collagen II,MMP13,GPX4 and ACSL4 expression levels. (M–P) qRT-PCR analysis for Collagen II,MMP13,GPX4 and ACSL4 gene expression. (Q–S) ELISA results for IL-6, TNF-α, and PGE2 levels. (T) Fe 2+ content in each group. (U) MDA content in each group. All data are represented as mean ± SD. (n = 3). Compared with the blank group,#p < 0.05,##p < 0.01,# # #p < 0.001,# # # #p < 0.0001; compared with the OA model group. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.

    Journal: Frontiers in Pharmacology

    Article Title: Asperosaponin VI suppresses ferroptosis in chondrocytes and ameliorates osteoarthritis by modulating the Nrf2/GPX4/HO-1 signaling pathway

    doi: 10.3389/fphar.2025.1539092

    Figure Lengend Snippet: AVI suppresses ferroptosis and confers protection to OA cartilage. (A) Fe 2+ content in each group. (B) MDA content in each group. (C–E) Western blot and quantitative analysis of GPX4 and ACSL4 expression levels. (F–G) qRT-PCR analysis of GPX4 and ACSL4 gene expression. (H–L) Western blot and quantitative analysis for Collagen II,MMP13,GPX4 and ACSL4 expression levels. (M–P) qRT-PCR analysis for Collagen II,MMP13,GPX4 and ACSL4 gene expression. (Q–S) ELISA results for IL-6, TNF-α, and PGE2 levels. (T) Fe 2+ content in each group. (U) MDA content in each group. All data are represented as mean ± SD. (n = 3). Compared with the blank group,#p < 0.05,##p < 0.01,# # #p < 0.001,# # # #p < 0.0001; compared with the OA model group. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.

    Article Snippet: The following ELISA kits were used: Rat TNF-α High Sensitivity ELISA Kit (EK382HS-96, MultiSciences, China), Rat IL-6 ELISA Kit (JYM0646Ra, Wuhan Jiyinmei Biotech, China),and Rat Prostaglandin E2 (PGE2) ELISA Kit (JYM0446Ra, Wuhan Jiyinmei Biotech, China).The levels of Fe 2+ and MDA in the cells post-intervention were determined using the Cell Ferrous Iron Colorimetric Assay Kit (E-BC-K881-M, Elabscience, China) and the MDA Colorimetric Assay Kit for Cell Samples (E-BCK0, Elabscience, China).

    Techniques: Western Blot, Expressing, Quantitative RT-PCR, Gene Expression, Enzyme-linked Immunosorbent Assay

    AVI mitigated OA progression in rats via the Nrf2/GPX4/HO-1 signaling axis. (A) IHC of Collagen II, MMP13, Nrf2, GPX4, HO-1, and ACSL4. (B) Relative quantitative analysis of expression of Collagen II, MMP13, Nrf2, GPX4, HO-1, and ACSL4. (C–E) ELISA results for IL-6, TNF-α, and PGE2 levels.

    Journal: Frontiers in Pharmacology

    Article Title: Asperosaponin VI suppresses ferroptosis in chondrocytes and ameliorates osteoarthritis by modulating the Nrf2/GPX4/HO-1 signaling pathway

    doi: 10.3389/fphar.2025.1539092

    Figure Lengend Snippet: AVI mitigated OA progression in rats via the Nrf2/GPX4/HO-1 signaling axis. (A) IHC of Collagen II, MMP13, Nrf2, GPX4, HO-1, and ACSL4. (B) Relative quantitative analysis of expression of Collagen II, MMP13, Nrf2, GPX4, HO-1, and ACSL4. (C–E) ELISA results for IL-6, TNF-α, and PGE2 levels.

    Article Snippet: The following ELISA kits were used: Rat TNF-α High Sensitivity ELISA Kit (EK382HS-96, MultiSciences, China), Rat IL-6 ELISA Kit (JYM0646Ra, Wuhan Jiyinmei Biotech, China),and Rat Prostaglandin E2 (PGE2) ELISA Kit (JYM0446Ra, Wuhan Jiyinmei Biotech, China).The levels of Fe 2+ and MDA in the cells post-intervention were determined using the Cell Ferrous Iron Colorimetric Assay Kit (E-BC-K881-M, Elabscience, China) and the MDA Colorimetric Assay Kit for Cell Samples (E-BCK0, Elabscience, China).

    Techniques: Expressing, Enzyme-linked Immunosorbent Assay