timp-1 concentrations enzyme-linked immunosorbent assay (elisa Search Results


human anti timp 1 dy970 antibodies  (R&D Systems)
93
R&D Systems human anti timp 1 dy970 antibodies
Human Anti Timp 1 Dy970 Antibodies, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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non competitive sandwich elisa  (Thermo Fisher)
99
Thermo Fisher non competitive sandwich elisa
Pro-collagen I ( A ) and elastin ( B ) levels measured by <t>ELISA</t> assay in HFF cells treated with ZPP at concentrations of 1, 10, and 100 µg/mL. Each column represents mean ± SD. Control cells (CTRL) were arbitrarily set to 1. Data were analyzed by one-way ANOVA followed by Dunnett’s post hoc multiple comparison: p > 0.05. Pro-collagen I: F(3,13) = 2.046; p = 0.1571).Elastin: F(3,4) = 0.927; p = 0.5050. (n = 6).
Non Competitive Sandwich Elisa, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human mmp 9 elisa  (Boster Bio)
94
Boster Bio human mmp 9 elisa
Pro-collagen I ( A ) and elastin ( B ) levels measured by <t>ELISA</t> assay in HFF cells treated with ZPP at concentrations of 1, 10, and 100 µg/mL. Each column represents mean ± SD. Control cells (CTRL) were arbitrarily set to 1. Data were analyzed by one-way ANOVA followed by Dunnett’s post hoc multiple comparison: p > 0.05. Pro-collagen I: F(3,13) = 2.046; p = 0.1571).Elastin: F(3,4) = 0.927; p = 0.5050. (n = 6).
Human Mmp 9 Elisa, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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immunosorbent assay kits  (R&D Systems)
95
R&D Systems immunosorbent assay kits
Pro-collagen I ( A ) and elastin ( B ) levels measured by <t>ELISA</t> assay in HFF cells treated with ZPP at concentrations of 1, 10, and 100 µg/mL. Each column represents mean ± SD. Control cells (CTRL) were arbitrarily set to 1. Data were analyzed by one-way ANOVA followed by Dunnett’s post hoc multiple comparison: p > 0.05. Pro-collagen I: F(3,13) = 2.046; p = 0.1571).Elastin: F(3,4) = 0.927; p = 0.5050. (n = 6).
Immunosorbent Assay Kits, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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immunosorbent assay kits - by Bioz Stars, 2026-02
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timp-1 elisa  (R&D Systems)
90
R&D Systems timp-1 elisa
Pro-collagen I ( A ) and elastin ( B ) levels measured by <t>ELISA</t> assay in HFF cells treated with ZPP at concentrations of 1, 10, and 100 µg/mL. Each column represents mean ± SD. Control cells (CTRL) were arbitrarily set to 1. Data were analyzed by one-way ANOVA followed by Dunnett’s post hoc multiple comparison: p > 0.05. Pro-collagen I: F(3,13) = 2.046; p = 0.1571).Elastin: F(3,4) = 0.927; p = 0.5050. (n = 6).
Timp 1 Elisa, 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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timp 1  (R&D Systems)
95
R&D Systems timp 1
Direct effects of LL-37 on matrix metalloproteinase (MMP) activity and <t>tissue</t> <t>inhibitor</t> of metalloproteinase (TIMP) production. Effects of LL-37 on ( a ) secreted MMP activities and ( b ) inhibition of MMP activities in the presence of EDTA in LL-37-treated gingival fibroblasts. Effects of LL-37 on ( c ) <t>TIMP-1</t> and ( d ) TIMP-2 secretion by gingival fibroblasts. Cells were incubated in medium containing the vehicle only (Control) or vehicle and peptide (0.2, 1, or 2 μM). MMP activities were expressed in relative fluorescent units (RFU) per minute, RFU/min, mean ± SD, n = 6; inhibition assays were expressed as % of substrate turnover in absence of the inhibitor EDTA, n = 3; TIMP-1 mean ± SD, n = 4; TIMP-2 mean ± SD, n = 4). Data were analysed by one-way analysis of variance followed by Bonferroni’s multiple comparison test (ns = nonsignificant; * p < 0.05; ** = p < 0.01). EDTA inhibition studies were not subject to statistical analysis; EDTA treatment was shown to reduce MMP activity by approximately 90%. In the comparison of MMP activities and TIMP-2 concentrations, all were found to be nonsignificant.
Timp 1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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elisa kits biotrak elisa systems  (ELISA SYSTEMS Pty Ltd)
90
ELISA SYSTEMS Pty Ltd elisa kits biotrak elisa systems
Direct effects of LL-37 on matrix metalloproteinase (MMP) activity and <t>tissue</t> <t>inhibitor</t> of metalloproteinase (TIMP) production. Effects of LL-37 on ( a ) secreted MMP activities and ( b ) inhibition of MMP activities in the presence of EDTA in LL-37-treated gingival fibroblasts. Effects of LL-37 on ( c ) <t>TIMP-1</t> and ( d ) TIMP-2 secretion by gingival fibroblasts. Cells were incubated in medium containing the vehicle only (Control) or vehicle and peptide (0.2, 1, or 2 μM). MMP activities were expressed in relative fluorescent units (RFU) per minute, RFU/min, mean ± SD, n = 6; inhibition assays were expressed as % of substrate turnover in absence of the inhibitor EDTA, n = 3; TIMP-1 mean ± SD, n = 4; TIMP-2 mean ± SD, n = 4). Data were analysed by one-way analysis of variance followed by Bonferroni’s multiple comparison test (ns = nonsignificant; * p < 0.05; ** = p < 0.01). EDTA inhibition studies were not subject to statistical analysis; EDTA treatment was shown to reduce MMP activity by approximately 90%. In the comparison of MMP activities and TIMP-2 concentrations, all were found to be nonsignificant.
Elisa Kits Biotrak Elisa Systems, supplied by ELISA SYSTEMS Pty Ltd, 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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mouse timp 1  (R&D Systems)
96
R&D Systems mouse timp 1
Direct effects of LL-37 on matrix metalloproteinase (MMP) activity and <t>tissue</t> <t>inhibitor</t> of metalloproteinase (TIMP) production. Effects of LL-37 on ( a ) secreted MMP activities and ( b ) inhibition of MMP activities in the presence of EDTA in LL-37-treated gingival fibroblasts. Effects of LL-37 on ( c ) <t>TIMP-1</t> and ( d ) TIMP-2 secretion by gingival fibroblasts. Cells were incubated in medium containing the vehicle only (Control) or vehicle and peptide (0.2, 1, or 2 μM). MMP activities were expressed in relative fluorescent units (RFU) per minute, RFU/min, mean ± SD, n = 6; inhibition assays were expressed as % of substrate turnover in absence of the inhibitor EDTA, n = 3; TIMP-1 mean ± SD, n = 4; TIMP-2 mean ± SD, n = 4). Data were analysed by one-way analysis of variance followed by Bonferroni’s multiple comparison test (ns = nonsignificant; * p < 0.05; ** = p < 0.01). EDTA inhibition studies were not subject to statistical analysis; EDTA treatment was shown to reduce MMP activity by approximately 90%. In the comparison of MMP activities and TIMP-2 concentrations, all were found to be nonsignificant.
Mouse Timp 1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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timp 1 elisa kit  (R&D Systems)
92
R&D Systems timp 1 elisa kit
Direct effects of LL-37 on matrix metalloproteinase (MMP) activity and <t>tissue</t> <t>inhibitor</t> of metalloproteinase (TIMP) production. Effects of LL-37 on ( a ) secreted MMP activities and ( b ) inhibition of MMP activities in the presence of EDTA in LL-37-treated gingival fibroblasts. Effects of LL-37 on ( c ) <t>TIMP-1</t> and ( d ) TIMP-2 secretion by gingival fibroblasts. Cells were incubated in medium containing the vehicle only (Control) or vehicle and peptide (0.2, 1, or 2 μM). MMP activities were expressed in relative fluorescent units (RFU) per minute, RFU/min, mean ± SD, n = 6; inhibition assays were expressed as % of substrate turnover in absence of the inhibitor EDTA, n = 3; TIMP-1 mean ± SD, n = 4; TIMP-2 mean ± SD, n = 4). Data were analysed by one-way analysis of variance followed by Bonferroni’s multiple comparison test (ns = nonsignificant; * p < 0.05; ** = p < 0.01). EDTA inhibition studies were not subject to statistical analysis; EDTA treatment was shown to reduce MMP activity by approximately 90%. In the comparison of MMP activities and TIMP-2 concentrations, all were found to be nonsignificant.
Timp 1 Elisa Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human timp- 1 elisa kit (№eh0294)  (Wuhan Fine Biotech)
90
Wuhan Fine Biotech human timp- 1 elisa kit (№eh0294)
Direct effects of LL-37 on matrix metalloproteinase (MMP) activity and <t>tissue</t> <t>inhibitor</t> of metalloproteinase (TIMP) production. Effects of LL-37 on ( a ) secreted MMP activities and ( b ) inhibition of MMP activities in the presence of EDTA in LL-37-treated gingival fibroblasts. Effects of LL-37 on ( c ) <t>TIMP-1</t> and ( d ) TIMP-2 secretion by gingival fibroblasts. Cells were incubated in medium containing the vehicle only (Control) or vehicle and peptide (0.2, 1, or 2 μM). MMP activities were expressed in relative fluorescent units (RFU) per minute, RFU/min, mean ± SD, n = 6; inhibition assays were expressed as % of substrate turnover in absence of the inhibitor EDTA, n = 3; TIMP-1 mean ± SD, n = 4; TIMP-2 mean ± SD, n = 4). Data were analysed by one-way analysis of variance followed by Bonferroni’s multiple comparison test (ns = nonsignificant; * p < 0.05; ** = p < 0.01). EDTA inhibition studies were not subject to statistical analysis; EDTA treatment was shown to reduce MMP activity by approximately 90%. In the comparison of MMP activities and TIMP-2 concentrations, all were found to be nonsignificant.
Human Timp 1 Elisa Kit (№Eh0294), 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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human timp-1 elisa kit  (Biosearch Technologies Inc)
90
Biosearch Technologies Inc human timp-1 elisa kit
Direct effects of LL-37 on matrix metalloproteinase (MMP) activity and <t>tissue</t> <t>inhibitor</t> of metalloproteinase (TIMP) production. Effects of LL-37 on ( a ) secreted MMP activities and ( b ) inhibition of MMP activities in the presence of EDTA in LL-37-treated gingival fibroblasts. Effects of LL-37 on ( c ) <t>TIMP-1</t> and ( d ) TIMP-2 secretion by gingival fibroblasts. Cells were incubated in medium containing the vehicle only (Control) or vehicle and peptide (0.2, 1, or 2 μM). MMP activities were expressed in relative fluorescent units (RFU) per minute, RFU/min, mean ± SD, n = 6; inhibition assays were expressed as % of substrate turnover in absence of the inhibitor EDTA, n = 3; TIMP-1 mean ± SD, n = 4; TIMP-2 mean ± SD, n = 4). Data were analysed by one-way analysis of variance followed by Bonferroni’s multiple comparison test (ns = nonsignificant; * p < 0.05; ** = p < 0.01). EDTA inhibition studies were not subject to statistical analysis; EDTA treatment was shown to reduce MMP activity by approximately 90%. In the comparison of MMP activities and TIMP-2 concentrations, all were found to be nonsignificant.
Human Timp 1 Elisa Kit, supplied by Biosearch Technologies Inc, 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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Image Search Results


Pro-collagen I ( A ) and elastin ( B ) levels measured by ELISA assay in HFF cells treated with ZPP at concentrations of 1, 10, and 100 µg/mL. Each column represents mean ± SD. Control cells (CTRL) were arbitrarily set to 1. Data were analyzed by one-way ANOVA followed by Dunnett’s post hoc multiple comparison: p > 0.05. Pro-collagen I: F(3,13) = 2.046; p = 0.1571).Elastin: F(3,4) = 0.927; p = 0.5050. (n = 6).

Journal: Pharmaceutics

Article Title: Biotechnological Phytocomplex of Zanthoxylum piperitum (L.) DC. Enhances Collagen Biosynthesis In Vitro and Improves Skin Elasticity In Vivo

doi: 10.3390/pharmaceutics17010138

Figure Lengend Snippet: Pro-collagen I ( A ) and elastin ( B ) levels measured by ELISA assay in HFF cells treated with ZPP at concentrations of 1, 10, and 100 µg/mL. Each column represents mean ± SD. Control cells (CTRL) were arbitrarily set to 1. Data were analyzed by one-way ANOVA followed by Dunnett’s post hoc multiple comparison: p > 0.05. Pro-collagen I: F(3,13) = 2.046; p = 0.1571).Elastin: F(3,4) = 0.927; p = 0.5050. (n = 6).

Article Snippet: Pro-collagen I, elastin, MMP-1, and TIMP-1 dosage were measured by using non-competitive sandwich ELISA (Human Pro-Collagen I α-1 Simple-Step kit ab210966, Abcam, Cambridge, UK; Human Elastin ELISA ab239433, Abcam; Human MMP-1 BMS2016-2, Afflimetrix-Thermofisher, Santa Clara, CA, USA; and Human TIMP-1 MA5-13688 (Afflimetrix-Thermofisher) according to the manufacturer’s instructions.

Techniques: Enzyme-linked Immunosorbent Assay, Control, Comparison

Analysis of MMP-1 ( A ) and TIMP-1 ( B ) protein levels by ELISA assay in HFF cell lysate after treatment with ZPP at the concentrations of 1, 10, and 100 µg/mL for 24 h. Data were analyzed using one-way ANOVA (MMP-1: F(3,7) = 0.340, p = 0.7978; TIMP-1: F(3,7) = 1.445, p = 0.3089) followed by Dunnett’s post hoc multiple comparison ( p > 0.05). Dosage of MMP-1 ( C ) and TIMP-1 ( D ) protein levels in HFF cell lysate after pre-treatment for 2 h with ZPP at the concentrations of 1, 10, and 100 µg/mL then exposed to MetPRED (100 µg/mL) for 6 h. One-way ANOVA (MMP-1: F(4,14) = 1.551, p = 0.2450; TIMP-1: F(4,13) = 2.795, p = 0.0709) followed by Tukey’s post hoc multiple comparison; (a) p < 0.05 vs. CTRL, (n = 6). Data are expressed as mean ± SD. Control cells (CTRL) were arbitrarily set to 1.

Journal: Pharmaceutics

Article Title: Biotechnological Phytocomplex of Zanthoxylum piperitum (L.) DC. Enhances Collagen Biosynthesis In Vitro and Improves Skin Elasticity In Vivo

doi: 10.3390/pharmaceutics17010138

Figure Lengend Snippet: Analysis of MMP-1 ( A ) and TIMP-1 ( B ) protein levels by ELISA assay in HFF cell lysate after treatment with ZPP at the concentrations of 1, 10, and 100 µg/mL for 24 h. Data were analyzed using one-way ANOVA (MMP-1: F(3,7) = 0.340, p = 0.7978; TIMP-1: F(3,7) = 1.445, p = 0.3089) followed by Dunnett’s post hoc multiple comparison ( p > 0.05). Dosage of MMP-1 ( C ) and TIMP-1 ( D ) protein levels in HFF cell lysate after pre-treatment for 2 h with ZPP at the concentrations of 1, 10, and 100 µg/mL then exposed to MetPRED (100 µg/mL) for 6 h. One-way ANOVA (MMP-1: F(4,14) = 1.551, p = 0.2450; TIMP-1: F(4,13) = 2.795, p = 0.0709) followed by Tukey’s post hoc multiple comparison; (a) p < 0.05 vs. CTRL, (n = 6). Data are expressed as mean ± SD. Control cells (CTRL) were arbitrarily set to 1.

Article Snippet: Pro-collagen I, elastin, MMP-1, and TIMP-1 dosage were measured by using non-competitive sandwich ELISA (Human Pro-Collagen I α-1 Simple-Step kit ab210966, Abcam, Cambridge, UK; Human Elastin ELISA ab239433, Abcam; Human MMP-1 BMS2016-2, Afflimetrix-Thermofisher, Santa Clara, CA, USA; and Human TIMP-1 MA5-13688 (Afflimetrix-Thermofisher) according to the manufacturer’s instructions.

Techniques: Enzyme-linked Immunosorbent Assay, Comparison, Control

Direct effects of LL-37 on matrix metalloproteinase (MMP) activity and tissue inhibitor of metalloproteinase (TIMP) production. Effects of LL-37 on ( a ) secreted MMP activities and ( b ) inhibition of MMP activities in the presence of EDTA in LL-37-treated gingival fibroblasts. Effects of LL-37 on ( c ) TIMP-1 and ( d ) TIMP-2 secretion by gingival fibroblasts. Cells were incubated in medium containing the vehicle only (Control) or vehicle and peptide (0.2, 1, or 2 μM). MMP activities were expressed in relative fluorescent units (RFU) per minute, RFU/min, mean ± SD, n = 6; inhibition assays were expressed as % of substrate turnover in absence of the inhibitor EDTA, n = 3; TIMP-1 mean ± SD, n = 4; TIMP-2 mean ± SD, n = 4). Data were analysed by one-way analysis of variance followed by Bonferroni’s multiple comparison test (ns = nonsignificant; * p < 0.05; ** = p < 0.01). EDTA inhibition studies were not subject to statistical analysis; EDTA treatment was shown to reduce MMP activity by approximately 90%. In the comparison of MMP activities and TIMP-2 concentrations, all were found to be nonsignificant.

Journal: Vaccines

Article Title: Effects of LL-37 on Gingival Fibroblasts: A Role in Periodontal Tissue Remodeling?

doi: 10.3390/vaccines6030044

Figure Lengend Snippet: Direct effects of LL-37 on matrix metalloproteinase (MMP) activity and tissue inhibitor of metalloproteinase (TIMP) production. Effects of LL-37 on ( a ) secreted MMP activities and ( b ) inhibition of MMP activities in the presence of EDTA in LL-37-treated gingival fibroblasts. Effects of LL-37 on ( c ) TIMP-1 and ( d ) TIMP-2 secretion by gingival fibroblasts. Cells were incubated in medium containing the vehicle only (Control) or vehicle and peptide (0.2, 1, or 2 μM). MMP activities were expressed in relative fluorescent units (RFU) per minute, RFU/min, mean ± SD, n = 6; inhibition assays were expressed as % of substrate turnover in absence of the inhibitor EDTA, n = 3; TIMP-1 mean ± SD, n = 4; TIMP-2 mean ± SD, n = 4). Data were analysed by one-way analysis of variance followed by Bonferroni’s multiple comparison test (ns = nonsignificant; * p < 0.05; ** = p < 0.01). EDTA inhibition studies were not subject to statistical analysis; EDTA treatment was shown to reduce MMP activity by approximately 90%. In the comparison of MMP activities and TIMP-2 concentrations, all were found to be nonsignificant.

Article Snippet: All human growth factor Quantikine ELISA kits (HGF, bFGF, KGF), TIMP-1 and TIMP-2 Quantikine ELISA kits, and IL-8 and IL-6 ELISA reagents were purchased from R&D Systems, Abingdon, UK.

Techniques: Activity Assay, Inhibition, Incubation, Comparison