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mmp1  (Boster Bio)


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    Boster Bio mmp1
    Nti-inflammatory activity of PE against LPS-Induced M1 polarization in RAW264.7 macrophages. (A) Assessment of RAW264.7 cell viability after PE treatment; (B) Determination of the half-inhibitory concentration of PE on RAW264.7 cells (>200 μM) (n = 6); (C) Changes in cell morphology of RAW264.7 cells stimulated with LPS and treated with PE at concentrations of 8, 16, and 32 μM; (D) Measurement of fluorescence intensity of CD86 and INOS in RAW264.7 cells via immunofluorescence staining; (E,F) Quantification of fluorescence intensity from images (D) ; (G–K) Analysis of gene expression of INOS, IL-6, TNF-α, TGF-β, and MMP3 in RAW264.7 cells after modeling and PE treatment by RT-PCR; (L) Evaluation of protein expression of TNF-α, IL-6, <t>MMP1,</t> MMP9, and MMP13 in RAW264.7 cells after modeling and PE treatment; (M) Densitometric analysis of the protein expression shown in image (L) . Data are the mean ± SD of 3 independent experiments. # P < 0.05, ## P < 0.01, vs. Ctrl group; * P < 0.05, ** P < 0.01, vs. LPS group; ns, not significant.
    Mmp1, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 73 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mmp1/product/Boster Bio
    Average 94 stars, based on 73 article reviews
    mmp1 - by Bioz Stars, 2026-02
    94/100 stars

    Images

    1) Product Images from "Parishin E from ginger-processed Gastrodia elata Bl. alleviates rheumatoid arthritis by regulating histone 3 lactylation at H3K18la and H3K27la sites"

    Article Title: Parishin E from ginger-processed Gastrodia elata Bl. alleviates rheumatoid arthritis by regulating histone 3 lactylation at H3K18la and H3K27la sites

    Journal: Frontiers in Pharmacology

    doi: 10.3389/fphar.2025.1682504

    Nti-inflammatory activity of PE against LPS-Induced M1 polarization in RAW264.7 macrophages. (A) Assessment of RAW264.7 cell viability after PE treatment; (B) Determination of the half-inhibitory concentration of PE on RAW264.7 cells (>200 μM) (n = 6); (C) Changes in cell morphology of RAW264.7 cells stimulated with LPS and treated with PE at concentrations of 8, 16, and 32 μM; (D) Measurement of fluorescence intensity of CD86 and INOS in RAW264.7 cells via immunofluorescence staining; (E,F) Quantification of fluorescence intensity from images (D) ; (G–K) Analysis of gene expression of INOS, IL-6, TNF-α, TGF-β, and MMP3 in RAW264.7 cells after modeling and PE treatment by RT-PCR; (L) Evaluation of protein expression of TNF-α, IL-6, MMP1, MMP9, and MMP13 in RAW264.7 cells after modeling and PE treatment; (M) Densitometric analysis of the protein expression shown in image (L) . Data are the mean ± SD of 3 independent experiments. # P < 0.05, ## P < 0.01, vs. Ctrl group; * P < 0.05, ** P < 0.01, vs. LPS group; ns, not significant.
    Figure Legend Snippet: Nti-inflammatory activity of PE against LPS-Induced M1 polarization in RAW264.7 macrophages. (A) Assessment of RAW264.7 cell viability after PE treatment; (B) Determination of the half-inhibitory concentration of PE on RAW264.7 cells (>200 μM) (n = 6); (C) Changes in cell morphology of RAW264.7 cells stimulated with LPS and treated with PE at concentrations of 8, 16, and 32 μM; (D) Measurement of fluorescence intensity of CD86 and INOS in RAW264.7 cells via immunofluorescence staining; (E,F) Quantification of fluorescence intensity from images (D) ; (G–K) Analysis of gene expression of INOS, IL-6, TNF-α, TGF-β, and MMP3 in RAW264.7 cells after modeling and PE treatment by RT-PCR; (L) Evaluation of protein expression of TNF-α, IL-6, MMP1, MMP9, and MMP13 in RAW264.7 cells after modeling and PE treatment; (M) Densitometric analysis of the protein expression shown in image (L) . Data are the mean ± SD of 3 independent experiments. # P < 0.05, ## P < 0.01, vs. Ctrl group; * P < 0.05, ** P < 0.01, vs. LPS group; ns, not significant.

    Techniques Used: Activity Assay, Concentration Assay, Fluorescence, Immunofluorescence, Staining, Gene Expression, Reverse Transcription Polymerase Chain Reaction, Expressing



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    Nti-inflammatory activity of PE against LPS-Induced M1 polarization in RAW264.7 macrophages. (A) Assessment of RAW264.7 cell viability after PE treatment; (B) Determination of the half-inhibitory concentration of PE on RAW264.7 cells (>200 μM) (n = 6); (C) Changes in cell morphology of RAW264.7 cells stimulated with LPS and treated with PE at concentrations of 8, 16, and 32 μM; (D) Measurement of fluorescence intensity of CD86 and INOS in RAW264.7 cells via immunofluorescence staining; (E,F) Quantification of fluorescence intensity from images (D) ; (G–K) Analysis of gene expression of INOS, IL-6, TNF-α, TGF-β, and MMP3 in RAW264.7 cells after modeling and PE treatment by RT-PCR; (L) Evaluation of protein expression of TNF-α, IL-6, <t>MMP1,</t> MMP9, and MMP13 in RAW264.7 cells after modeling and PE treatment; (M) Densitometric analysis of the protein expression shown in image (L) . Data are the mean ± SD of 3 independent experiments. # P < 0.05, ## P < 0.01, vs. Ctrl group; * P < 0.05, ** P < 0.01, vs. LPS group; ns, not significant.
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    Nti-inflammatory activity of PE against LPS-Induced M1 polarization in RAW264.7 macrophages. (A) Assessment of RAW264.7 cell viability after PE treatment; (B) Determination of the half-inhibitory concentration of PE on RAW264.7 cells (>200 μM) (n = 6); (C) Changes in cell morphology of RAW264.7 cells stimulated with LPS and treated with PE at concentrations of 8, 16, and 32 μM; (D) Measurement of fluorescence intensity of CD86 and INOS in RAW264.7 cells via immunofluorescence staining; (E,F) Quantification of fluorescence intensity from images (D) ; (G–K) Analysis of gene expression of INOS, IL-6, TNF-α, TGF-β, and MMP3 in RAW264.7 cells after modeling and PE treatment by RT-PCR; (L) Evaluation of protein expression of TNF-α, IL-6, <t>MMP1,</t> MMP9, and MMP13 in RAW264.7 cells after modeling and PE treatment; (M) Densitometric analysis of the protein expression shown in image (L) . Data are the mean ± SD of 3 independent experiments. # P < 0.05, ## P < 0.01, vs. Ctrl group; * P < 0.05, ** P < 0.01, vs. LPS group; ns, not significant.
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    Image Search Results


    Nti-inflammatory activity of PE against LPS-Induced M1 polarization in RAW264.7 macrophages. (A) Assessment of RAW264.7 cell viability after PE treatment; (B) Determination of the half-inhibitory concentration of PE on RAW264.7 cells (>200 μM) (n = 6); (C) Changes in cell morphology of RAW264.7 cells stimulated with LPS and treated with PE at concentrations of 8, 16, and 32 μM; (D) Measurement of fluorescence intensity of CD86 and INOS in RAW264.7 cells via immunofluorescence staining; (E,F) Quantification of fluorescence intensity from images (D) ; (G–K) Analysis of gene expression of INOS, IL-6, TNF-α, TGF-β, and MMP3 in RAW264.7 cells after modeling and PE treatment by RT-PCR; (L) Evaluation of protein expression of TNF-α, IL-6, MMP1, MMP9, and MMP13 in RAW264.7 cells after modeling and PE treatment; (M) Densitometric analysis of the protein expression shown in image (L) . Data are the mean ± SD of 3 independent experiments. # P < 0.05, ## P < 0.01, vs. Ctrl group; * P < 0.05, ** P < 0.01, vs. LPS group; ns, not significant.

    Journal: Frontiers in Pharmacology

    Article Title: Parishin E from ginger-processed Gastrodia elata Bl. alleviates rheumatoid arthritis by regulating histone 3 lactylation at H3K18la and H3K27la sites

    doi: 10.3389/fphar.2025.1682504

    Figure Lengend Snippet: Nti-inflammatory activity of PE against LPS-Induced M1 polarization in RAW264.7 macrophages. (A) Assessment of RAW264.7 cell viability after PE treatment; (B) Determination of the half-inhibitory concentration of PE on RAW264.7 cells (>200 μM) (n = 6); (C) Changes in cell morphology of RAW264.7 cells stimulated with LPS and treated with PE at concentrations of 8, 16, and 32 μM; (D) Measurement of fluorescence intensity of CD86 and INOS in RAW264.7 cells via immunofluorescence staining; (E,F) Quantification of fluorescence intensity from images (D) ; (G–K) Analysis of gene expression of INOS, IL-6, TNF-α, TGF-β, and MMP3 in RAW264.7 cells after modeling and PE treatment by RT-PCR; (L) Evaluation of protein expression of TNF-α, IL-6, MMP1, MMP9, and MMP13 in RAW264.7 cells after modeling and PE treatment; (M) Densitometric analysis of the protein expression shown in image (L) . Data are the mean ± SD of 3 independent experiments. # P < 0.05, ## P < 0.01, vs. Ctrl group; * P < 0.05, ** P < 0.01, vs. LPS group; ns, not significant.

    Article Snippet: Primary antibodies used were as follows: IL-6 (1: 1000, Proteintech, Cat# IL6-b, RRID:AB_3665394), TNF-α (1: 1000, ABclonal, Cat# A20851, RRID:AB_3669044), MMP1 (1: 1000, Boster Bio, Cat# PB0764, RRID: N/A), MMP9 (1: 1000, Boster Bio, Cat# BM4089, RRID: N/A), MMP13 (1: 1000, Abcam, Cat# ab315267, RRID:AB_3696043), GLUT1 (1:1000, WanLeiBio Cat# WL01163, RRID:AB_3675696), HK2 (1:1 000, Proteintech Cat# 22029-1-AP, RRID:AB_11182717), PKM2 (1: 1000, Proteintech Cat# 15822-1-AP, RRID:AB_1851537), LDHA (1: 1000, Beyotime, Cat# AF0216, RRID:N/A), LYS18 (1: 1000, PTM BIO Cat# PTM-158, RRID:AB_3678563), LYS27(1: 1000, PTM BIO Cat# PTM-160, RRID:AB_3697632), Pan Kla (1: 1000, PTM BIO Cat# PTM-1425, RRID:AB_2937057),β-Actin (1: 10000, Solarbio Cat# K101527P, RRID:AB_3697466), Histone H3 (1: 1000, PTM BIO Cat# PTM-312, RRID:AB_3711312), SIRT6 (1: 1000, ZenBio Cat# AR381408, RRID:N/A), HDAC1(1: 1000, ZenBio Cat# R24533, RRID:N/A), SIRT1 (1: 1000, Zen Bio Cat# R25721, RRID:AB_2921365), SIRT2 (1: 1000, Zen Bio Cat# R25722, RRID:N/A), SIRT7 (1: 1000, Proteintech Cat# 12994-1-AP, RRID:AB_10644276).

    Techniques: Activity Assay, Concentration Assay, Fluorescence, Immunofluorescence, Staining, Gene Expression, Reverse Transcription Polymerase Chain Reaction, Expressing

    Fig. 10 Immunohistochemistry and immunofluorescence staining in synovium of rats. (A-B) Images of immunohistochemistry results of MMP-1 and MMP-2 in synovium after treatment; (C-G) Images of immunofluorescence results of vimentin, CD44, CD68, CD86 and CD206 in knee synovial tissues after treatment (n = 6)

    Journal: Journal of nanobiotechnology

    Article Title: Treatment of rheumatoid arthritis using dual-targeted and dual-response intelligent micelles: a "three birds with one stone" strategy.

    doi: 10.1186/s12951-024-03085-0

    Figure Lengend Snippet: Fig. 10 Immunohistochemistry and immunofluorescence staining in synovium of rats. (A-B) Images of immunohistochemistry results of MMP-1 and MMP-2 in synovium after treatment; (C-G) Images of immunofluorescence results of vimentin, CD44, CD68, CD86 and CD206 in knee synovial tissues after treatment (n = 6)

    Article Snippet: MMP-1, MMP-3, and vimentin antibodies were obtained from Boster (Wuhan, China).

    Techniques: Immunohistochemistry, Immunofluorescence, Staining