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mmps 1 timp 1  (Boster Bio)


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    Structured Review

    Boster Bio mmps 1 timp 1
    Knockdown of LY6K inhibits migration and invasion of CCSCs in vitro. Optical micrographs and the number of migrated ( A ) and invaded ( B ) CCSCs following siLY6K or siNC transfection for 48 h according to Transwell migration and invasion assay. n = 3. ( C ) Western blot analyses showing the protein levels of MMP-2, MMP-9, and <t>TIMP-1</t> in CCSCs after treatment with siLY6K or siNC for 48 h. Values are the mean ± SE (n = 3). ** p < 0.01, *** p < 0.001, or **** p < 0.0001 indicates significant differences from the Mock and siNC group as assessed by one-way ANOVA with Tukey–Kramer multiple comparisons tests. LY6K, lymphocyte antigen 6, locus K; CCSC, colon cancer stem cells; MMP, matrix metalloproteinase; TIMP-1, <t>tissue</t> <t>inhibitor</t> of MMP-1; n.s., not significant.
    Mmps 1 Timp 1, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 128 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mmps 1 timp 1/product/Boster Bio
    Average 94 stars, based on 128 article reviews
    mmps 1 timp 1 - by Bioz Stars, 2026-03
    94/100 stars

    Images

    1) Product Images from "Silencing LY6K Suppresses CD44 + EpCAM + HCT116 Human Colon Cancer Stem Cells Growth: Insights from In Vitro and In Vivo Evidence"

    Article Title: Silencing LY6K Suppresses CD44 + EpCAM + HCT116 Human Colon Cancer Stem Cells Growth: Insights from In Vitro and In Vivo Evidence

    Journal: Current Issues in Molecular Biology

    doi: 10.3390/cimb46120840

    Knockdown of LY6K inhibits migration and invasion of CCSCs in vitro. Optical micrographs and the number of migrated ( A ) and invaded ( B ) CCSCs following siLY6K or siNC transfection for 48 h according to Transwell migration and invasion assay. n = 3. ( C ) Western blot analyses showing the protein levels of MMP-2, MMP-9, and TIMP-1 in CCSCs after treatment with siLY6K or siNC for 48 h. Values are the mean ± SE (n = 3). ** p < 0.01, *** p < 0.001, or **** p < 0.0001 indicates significant differences from the Mock and siNC group as assessed by one-way ANOVA with Tukey–Kramer multiple comparisons tests. LY6K, lymphocyte antigen 6, locus K; CCSC, colon cancer stem cells; MMP, matrix metalloproteinase; TIMP-1, tissue inhibitor of MMP-1; n.s., not significant.
    Figure Legend Snippet: Knockdown of LY6K inhibits migration and invasion of CCSCs in vitro. Optical micrographs and the number of migrated ( A ) and invaded ( B ) CCSCs following siLY6K or siNC transfection for 48 h according to Transwell migration and invasion assay. n = 3. ( C ) Western blot analyses showing the protein levels of MMP-2, MMP-9, and TIMP-1 in CCSCs after treatment with siLY6K or siNC for 48 h. Values are the mean ± SE (n = 3). ** p < 0.01, *** p < 0.001, or **** p < 0.0001 indicates significant differences from the Mock and siNC group as assessed by one-way ANOVA with Tukey–Kramer multiple comparisons tests. LY6K, lymphocyte antigen 6, locus K; CCSC, colon cancer stem cells; MMP, matrix metalloproteinase; TIMP-1, tissue inhibitor of MMP-1; n.s., not significant.

    Techniques Used: Knockdown, Migration, In Vitro, Transfection, Invasion Assay, Western Blot



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    Knockdown of LY6K inhibits migration and invasion of CCSCs in vitro. Optical micrographs and the number of migrated ( A ) and invaded ( B ) CCSCs following siLY6K or siNC transfection for 48 h according to Transwell migration and invasion assay. n = 3. ( C ) Western blot analyses showing the protein levels of MMP-2, MMP-9, and <t>TIMP-1</t> in CCSCs after treatment with siLY6K or siNC for 48 h. Values are the mean ± SE (n = 3). ** p < 0.01, *** p < 0.001, or **** p < 0.0001 indicates significant differences from the Mock and siNC group as assessed by one-way ANOVA with Tukey–Kramer multiple comparisons tests. LY6K, lymphocyte antigen 6, locus K; CCSC, colon cancer stem cells; MMP, matrix metalloproteinase; TIMP-1, <t>tissue</t> <t>inhibitor</t> of MMP-1; n.s., not significant.
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    Figure 2. Levels of <t>matrix</t> <t>metalloproteinases</t> and <t>tissue</t> <t>inhibitor</t> of metalloproteinases in the brain of rats with hyperhomocysteinemia. Values are expressed as mean ± SEM (n=10); *p<0.05 compared to the control group of corresponding age; #p<0.05 compared to the group “Young_Control”.
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    Image Search Results


    Knockdown of LY6K inhibits migration and invasion of CCSCs in vitro. Optical micrographs and the number of migrated ( A ) and invaded ( B ) CCSCs following siLY6K or siNC transfection for 48 h according to Transwell migration and invasion assay. n = 3. ( C ) Western blot analyses showing the protein levels of MMP-2, MMP-9, and TIMP-1 in CCSCs after treatment with siLY6K or siNC for 48 h. Values are the mean ± SE (n = 3). ** p < 0.01, *** p < 0.001, or **** p < 0.0001 indicates significant differences from the Mock and siNC group as assessed by one-way ANOVA with Tukey–Kramer multiple comparisons tests. LY6K, lymphocyte antigen 6, locus K; CCSC, colon cancer stem cells; MMP, matrix metalloproteinase; TIMP-1, tissue inhibitor of MMP-1; n.s., not significant.

    Journal: Current Issues in Molecular Biology

    Article Title: Silencing LY6K Suppresses CD44 + EpCAM + HCT116 Human Colon Cancer Stem Cells Growth: Insights from In Vitro and In Vivo Evidence

    doi: 10.3390/cimb46120840

    Figure Lengend Snippet: Knockdown of LY6K inhibits migration and invasion of CCSCs in vitro. Optical micrographs and the number of migrated ( A ) and invaded ( B ) CCSCs following siLY6K or siNC transfection for 48 h according to Transwell migration and invasion assay. n = 3. ( C ) Western blot analyses showing the protein levels of MMP-2, MMP-9, and TIMP-1 in CCSCs after treatment with siLY6K or siNC for 48 h. Values are the mean ± SE (n = 3). ** p < 0.01, *** p < 0.001, or **** p < 0.0001 indicates significant differences from the Mock and siNC group as assessed by one-way ANOVA with Tukey–Kramer multiple comparisons tests. LY6K, lymphocyte antigen 6, locus K; CCSC, colon cancer stem cells; MMP, matrix metalloproteinase; TIMP-1, tissue inhibitor of MMP-1; n.s., not significant.

    Article Snippet: The membranes were incubated overnight at 4 °C with primary antibodies [LY6K (1:750, #PIPA572689, Invitrogen), MMP-2 (3:1000, #BM0569, Boster, Pleasanton, CA, USA), MMP-9 (1:300, #BM4089, Boster), tissue inhibitor of MMPs-1 (TIMP-1) (3:1000, #BM4980, Boster), cyclin-dependent kinase (CDK) 4 (3:1000, #BM4672, Boster), cyclin D1 (3:1000, #bs-0623R, Bioss), CDK2 (3:1000, #bs-0757R, Bioss), cyclin E1 (3:1000, #bs-0573R, Bioss), caspase-3 and cleaved caspase-3 (1:1000, #14220, CST), β-actin (1:1500, #AF0003, Beyotime), and β-tubulin (1:1000, #AC008, Beyotime)], followed by incubation with secondary antibodies [horseradish peroxidase-conjugated goat anti-rabbit (1:2000, #A0208, Beyotime) and anti-mouse (1:2000, #A0216, Beyotime)] for 1 h at room temperature.

    Techniques: Knockdown, Migration, In Vitro, Transfection, Invasion Assay, Western Blot

    Journal: iScience

    Article Title: Human monocyte-derived macrophages shift subcellular metalloprotease activity depending on their activation state

    doi: 10.1016/j.isci.2024.111171

    Figure Lengend Snippet:

    Article Snippet: Human MMP-9/TIMP-1 DuoSet ELISA , R&D Systems , Cat # DY1449.

    Techniques: Plasmid Preparation, Recombinant, Knock-Out, Blocking Assay, Staining, Antibody Labeling, Reverse Transcription, Lysis, Protease Inhibitor, Enzyme-linked Immunosorbent Assay, Fractionation, Cell Culture, Software, Flow Cytometry, Fluorescence, Spectrophotometry

    Figure 2. Levels of matrix metalloproteinases and tissue inhibitor of metalloproteinases in the brain of rats with hyperhomocysteinemia. Values are expressed as mean ± SEM (n=10); *p<0.05 compared to the control group of corresponding age; #p<0.05 compared to the group “Young_Control”.

    Journal: Journal of Biological Research - Bollettino della Società Italiana di Biologia Sperimentale

    Article Title: Proteolytic system parameters in the brain of rats with hyperhomocysteinemia

    doi: 10.4081/jbr.2024.12232

    Figure Lengend Snippet: Figure 2. Levels of matrix metalloproteinases and tissue inhibitor of metalloproteinases in the brain of rats with hyperhomocysteinemia. Values are expressed as mean ± SEM (n=10); *p<0.05 compared to the control group of corresponding age; #p<0.05 compared to the group “Young_Control”.

    Article Snippet: The following reagents were used in our research: DL-HTL hydrochloride (Acros Organics, Italy); casein, trichloroacetic acid (TCA), ethylenediaminetetraacetic acid (EDTA), phenylmethylsulfonyl fluoride (PMSF), hydrogen peroxide and o-phenylenediamine (Sigma-Aldrich, St. Louis, MO, USA); anti-rat monoclonal antibodies to cytokines, tissue inhibitor of metalloproteinases-1 (TIMP-1) and MMPs (Santa Cruz Biotechnology, Inc., Dallas, Texas, USA); horseradish peroxidase-conjugated secondary antibodies (SigmaAldrich, St. Louis, MO, USA).

    Techniques: Control