mmp14 elisa kit Search Results


mmp 14 content  (Elabscience Biotechnology)
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Elabscience Biotechnology mmp 14 content
Mmp 14 Content, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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elisa kits  (R&D Systems)
90
R&D Systems elisa kits
GO-AGEs enhance the degradation of extracellular matrix by increasing the matrix metalloproteinase release while decreasing expression of <t>COL1A</t> and SIRT1 in NHDF cells. ( A ) MTT assay showing cytotoxic effects of GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ), along with the control group in NHDF cells. ( B , C ) <t>ELISA</t> results demonstrating the MMP-1 ( B ) and COL1A ( C ) levels in the conditioned medium of NHDF cells upon treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( D ) Western blot analysis showing the expression level of MMP-1, COL1A, and SIRT1 proteins after treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( E – G ) Quantification of the expression levels of MMP-1 ( E ), COL1A ( F ), and SIRT1 ( G ). Each value represents the mean ± SEM of triplicate experiments. *p < 0.05, **p < 0.01, and ***p < 0.001 vs. the control group and # p < 0.05 and ### p < 0.001 vs. the UVB treatment group induced by UVB irradiation (125 mJ/cm 2 ).
Elisa Kits, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
elisa kits - by Bioz Stars, 2026-05
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csb e13157h  (Cusabio)
86
Cusabio csb e13157h
GO-AGEs enhance the degradation of extracellular matrix by increasing the matrix metalloproteinase release while decreasing expression of <t>COL1A</t> and SIRT1 in NHDF cells. ( A ) MTT assay showing cytotoxic effects of GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ), along with the control group in NHDF cells. ( B , C ) <t>ELISA</t> results demonstrating the MMP-1 ( B ) and COL1A ( C ) levels in the conditioned medium of NHDF cells upon treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( D ) Western blot analysis showing the expression level of MMP-1, COL1A, and SIRT1 proteins after treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( E – G ) Quantification of the expression levels of MMP-1 ( E ), COL1A ( F ), and SIRT1 ( G ). Each value represents the mean ± SEM of triplicate experiments. *p < 0.05, **p < 0.01, and ***p < 0.001 vs. the control group and # p < 0.05 and ### p < 0.001 vs. the UVB treatment group induced by UVB irradiation (125 mJ/cm 2 ).
Csb E13157h, supplied by Cusabio, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mmp14 elisa kit  (Wuhan Fine Biotech)
90
Wuhan Fine Biotech mmp14 elisa kit
GO-AGEs enhance the degradation of extracellular matrix by increasing the matrix metalloproteinase release while decreasing expression of <t>COL1A</t> and SIRT1 in NHDF cells. ( A ) MTT assay showing cytotoxic effects of GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ), along with the control group in NHDF cells. ( B , C ) <t>ELISA</t> results demonstrating the MMP-1 ( B ) and COL1A ( C ) levels in the conditioned medium of NHDF cells upon treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( D ) Western blot analysis showing the expression level of MMP-1, COL1A, and SIRT1 proteins after treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( E – G ) Quantification of the expression levels of MMP-1 ( E ), COL1A ( F ), and SIRT1 ( G ). Each value represents the mean ± SEM of triplicate experiments. *p < 0.05, **p < 0.01, and ***p < 0.001 vs. the control group and # p < 0.05 and ### p < 0.001 vs. the UVB treatment group induced by UVB irradiation (125 mJ/cm 2 ).
Mmp14 Elisa Kit, supplied by Wuhan Fine Biotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
mmp14 elisa kit - by Bioz Stars, 2026-05
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elisa kit matrix metalloproteinase 14 (mmp14  (Cloud-Clone corp)
90
Cloud-Clone corp elisa kit matrix metalloproteinase 14 (mmp14
GO-AGEs enhance the degradation of extracellular matrix by increasing the matrix metalloproteinase release while decreasing expression of <t>COL1A</t> and SIRT1 in NHDF cells. ( A ) MTT assay showing cytotoxic effects of GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ), along with the control group in NHDF cells. ( B , C ) <t>ELISA</t> results demonstrating the MMP-1 ( B ) and COL1A ( C ) levels in the conditioned medium of NHDF cells upon treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( D ) Western blot analysis showing the expression level of MMP-1, COL1A, and SIRT1 proteins after treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( E – G ) Quantification of the expression levels of MMP-1 ( E ), COL1A ( F ), and SIRT1 ( G ). Each value represents the mean ± SEM of triplicate experiments. *p < 0.05, **p < 0.01, and ***p < 0.001 vs. the control group and # p < 0.05 and ### p < 0.001 vs. the UVB treatment group induced by UVB irradiation (125 mJ/cm 2 ).
Elisa Kit Matrix Metalloproteinase 14 (Mmp14, supplied by Cloud-Clone corp, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
elisa kit matrix metalloproteinase 14 (mmp14 - by Bioz Stars, 2026-05
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quantitative human pecam-1 & mmp-14 sandwich elisa kit  (Abbkine Inc)
90
Abbkine Inc quantitative human pecam-1 & mmp-14 sandwich elisa kit
GO-AGEs enhance the degradation of extracellular matrix by increasing the matrix metalloproteinase release while decreasing expression of <t>COL1A</t> and SIRT1 in NHDF cells. ( A ) MTT assay showing cytotoxic effects of GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ), along with the control group in NHDF cells. ( B , C ) <t>ELISA</t> results demonstrating the MMP-1 ( B ) and COL1A ( C ) levels in the conditioned medium of NHDF cells upon treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( D ) Western blot analysis showing the expression level of MMP-1, COL1A, and SIRT1 proteins after treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( E – G ) Quantification of the expression levels of MMP-1 ( E ), COL1A ( F ), and SIRT1 ( G ). Each value represents the mean ± SEM of triplicate experiments. *p < 0.05, **p < 0.01, and ***p < 0.001 vs. the control group and # p < 0.05 and ### p < 0.001 vs. the UVB treatment group induced by UVB irradiation (125 mJ/cm 2 ).
Quantitative Human Pecam 1 & Mmp 14 Sandwich Elisa Kit, supplied by Abbkine Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/quantitative human pecam-1 & mmp-14 sandwich elisa kit/product/Abbkine Inc
Average 90 stars, based on 1 article reviews
quantitative human pecam-1 & mmp-14 sandwich elisa kit - by Bioz Stars, 2026-05
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mmp-14 colorimetric cell-based elisa kit (okag00883)  (Aviva Systems)
N/A
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human matrix metalloproteinase 14 (mmp14) elisa kit  (Bioss)
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human mmp14 elisa kit  (OriGene)
N/A
For quantitative detection of human MMP 14 in cell culture supernates serum and plasma heparin
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human mmp 14 matrix metalloproteinase 14 elisa kit  (Elabscience)
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rat mmp-14/mt1-mmp elisa kit (colorimetric)  (Novus Biologicals)
N/A
Rat MMP-14/MT1-MMP ELISA Kit (Colorimetric)
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mouse mmp 14 matrix metalloproteinase 14 elisa kit  (Elabscience)
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Image Search Results


GO-AGEs enhance the degradation of extracellular matrix by increasing the matrix metalloproteinase release while decreasing expression of COL1A and SIRT1 in NHDF cells. ( A ) MTT assay showing cytotoxic effects of GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ), along with the control group in NHDF cells. ( B , C ) ELISA results demonstrating the MMP-1 ( B ) and COL1A ( C ) levels in the conditioned medium of NHDF cells upon treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( D ) Western blot analysis showing the expression level of MMP-1, COL1A, and SIRT1 proteins after treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( E – G ) Quantification of the expression levels of MMP-1 ( E ), COL1A ( F ), and SIRT1 ( G ). Each value represents the mean ± SEM of triplicate experiments. *p < 0.05, **p < 0.01, and ***p < 0.001 vs. the control group and # p < 0.05 and ### p < 0.001 vs. the UVB treatment group induced by UVB irradiation (125 mJ/cm 2 ).

Journal: Scientific Reports

Article Title: Glyoxal-derived advanced glycation end products (GO-AGEs) with UVB critically induce skin inflammaging: in vitro and in silico approaches

doi: 10.1038/s41598-024-52037-z

Figure Lengend Snippet: GO-AGEs enhance the degradation of extracellular matrix by increasing the matrix metalloproteinase release while decreasing expression of COL1A and SIRT1 in NHDF cells. ( A ) MTT assay showing cytotoxic effects of GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ), along with the control group in NHDF cells. ( B , C ) ELISA results demonstrating the MMP-1 ( B ) and COL1A ( C ) levels in the conditioned medium of NHDF cells upon treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( D ) Western blot analysis showing the expression level of MMP-1, COL1A, and SIRT1 proteins after treatment with GO-AGEs (100 μg/mL) in the presence or absence of UVB irradiation (125 mJ/cm 2 ) along with the control group. ( E – G ) Quantification of the expression levels of MMP-1 ( E ), COL1A ( F ), and SIRT1 ( G ). Each value represents the mean ± SEM of triplicate experiments. *p < 0.05, **p < 0.01, and ***p < 0.001 vs. the control group and # p < 0.05 and ### p < 0.001 vs. the UVB treatment group induced by UVB irradiation (125 mJ/cm 2 ).

Article Snippet: After 48 h of incubation, the MMP-1 and COL1A concentrations were analyzed using ELISA kits (Human Total MMP-1; R&D Systems Inc.; COL1A C-Peptide ELISA Kit, Takara).

Techniques: Expressing, MTT Assay, Irradiation, Enzyme-linked Immunosorbent Assay, Western Blot

Molecular docking analysis of methylglyoxal-lysine dimer (MOLD) with different target proteins performed by the AutoDock Vina program. The complex structures of MOLD with IL-1β ( A ), IL-6 ( B ), TNF-α ( C ), COX2 ( D ), P65 ( E ), RAGE ( F ), MMP-1 ( G ), COL1A ( H ), SIRT1 ( I ).

Journal: Scientific Reports

Article Title: Glyoxal-derived advanced glycation end products (GO-AGEs) with UVB critically induce skin inflammaging: in vitro and in silico approaches

doi: 10.1038/s41598-024-52037-z

Figure Lengend Snippet: Molecular docking analysis of methylglyoxal-lysine dimer (MOLD) with different target proteins performed by the AutoDock Vina program. The complex structures of MOLD with IL-1β ( A ), IL-6 ( B ), TNF-α ( C ), COX2 ( D ), P65 ( E ), RAGE ( F ), MMP-1 ( G ), COL1A ( H ), SIRT1 ( I ).

Article Snippet: After 48 h of incubation, the MMP-1 and COL1A concentrations were analyzed using ELISA kits (Human Total MMP-1; R&D Systems Inc.; COL1A C-Peptide ELISA Kit, Takara).

Techniques: