human matrix metalloproteinase 26 Search Results


94
Shanghai Korain Biotech Co Ltd human matrix metalloproteinase 26
Human Matrix Metalloproteinase 26, supplied by Shanghai Korain Biotech Co Ltd, 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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94
Krishgen Biosystems neutrophil collagenase elisa kit
Neutrophil Collagenase Elisa Kit, supplied by Krishgen Biosystems, 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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93
Cusabio elisa calorimetric assay kits
Effect of HY7714 EPS on ECM modulation in HS68 cells. ( A ) The intracellular level of matrix <t>metalloproteinase1</t> <t>(MMP1)</t> in HS68 cells treated with HY7714 EPS was measured using an MMP1 <t>ELISA</t> kit. ( B , C ) Relative mRNA levels of MMP1 and HAS1 in HS68 cells were calculated by qPCR and normalized against GAPDH. ( D ) Western blotting for MMP1 and COLa1 in HS68 cells, and quantification of band density. Data are expressed as means ± SD ( n = 4), and values labeled with different letters are significantly different, p < 0.05 (a > b > c). CON, control cells.
Elisa Calorimetric Assay Kits, supplied by Cusabio, 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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93
Proteintech matrix metalloproteinase 2
hucMSC-exosomes inhibited intimal hyperplasia and luminal stenosis in arterialized vein grafts. a Representative ultrasound images of vein grafts from the PBS group (left panel) and exosome group (right panel). Quantification of the luminal diameter ( b ) and peak-systolic velocity ( c ) in vein grafts. d Histologic images of haematoxylin and eosin staining (HE) staining in vein grafts from the normal vein group (left panel), PBS group (middle panel), and exosome group (right panel). e Quantification of the neointimal thickness in vein grafts. f Immunohistochemical staining of matrix <t>metalloproteinase</t> <t>2</t> (MMP-2) in vein grafts from the PBS group (left panel) and exosome group (right panel). g Immunohistochemical staining of matrix metalloproteinase 9 (MMP-9) in vein grafts from the PBS group (left panel) and exosome group (right panel). h Immunohistochemical staining of proliferating cell nuclear antigen (PCNA) in vein grafts from the PBS group (left panel) and exosome group (right panel). i Quantitative analysis of PCNA-positive index in vein grafts. The PCNA-positive index was quantified as the percentage of total nuclei in the neointima. Scale bar is 200 μm in panels d , f , g , and h . The results are presented as the mean ± SD, n = 6 for each group. An asterisk represents statistically significant difference compared with the PBS group ( P < 0.05). Number sign represents statistically significant difference compared with the normal vein group ( P < 0.05)
Matrix Metalloproteinase 2, supplied by Proteintech, 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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Shanghai Korain Biotech Co Ltd human matrix metalloproteinase 1
hucMSC-exosomes inhibited intimal hyperplasia and luminal stenosis in arterialized vein grafts. a Representative ultrasound images of vein grafts from the PBS group (left panel) and exosome group (right panel). Quantification of the luminal diameter ( b ) and peak-systolic velocity ( c ) in vein grafts. d Histologic images of haematoxylin and eosin staining (HE) staining in vein grafts from the normal vein group (left panel), PBS group (middle panel), and exosome group (right panel). e Quantification of the neointimal thickness in vein grafts. f Immunohistochemical staining of matrix <t>metalloproteinase</t> <t>2</t> (MMP-2) in vein grafts from the PBS group (left panel) and exosome group (right panel). g Immunohistochemical staining of matrix metalloproteinase 9 (MMP-9) in vein grafts from the PBS group (left panel) and exosome group (right panel). h Immunohistochemical staining of proliferating cell nuclear antigen (PCNA) in vein grafts from the PBS group (left panel) and exosome group (right panel). i Quantitative analysis of PCNA-positive index in vein grafts. The PCNA-positive index was quantified as the percentage of total nuclei in the neointima. Scale bar is 200 μm in panels d , f , g , and h . The results are presented as the mean ± SD, n = 6 for each group. An asterisk represents statistically significant difference compared with the PBS group ( P < 0.05). Number sign represents statistically significant difference compared with the normal vein group ( P < 0.05)
Human Matrix Metalloproteinase 1, supplied by Shanghai Korain Biotech Co 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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Image Search Results


Effect of HY7714 EPS on ECM modulation in HS68 cells. ( A ) The intracellular level of matrix metalloproteinase1 (MMP1) in HS68 cells treated with HY7714 EPS was measured using an MMP1 ELISA kit. ( B , C ) Relative mRNA levels of MMP1 and HAS1 in HS68 cells were calculated by qPCR and normalized against GAPDH. ( D ) Western blotting for MMP1 and COLa1 in HS68 cells, and quantification of band density. Data are expressed as means ± SD ( n = 4), and values labeled with different letters are significantly different, p < 0.05 (a > b > c). CON, control cells.

Journal: Molecules

Article Title: Exopolysaccharide from Lactobacillus plantarum HY7714 Protects against Skin Aging through Skin–Gut Axis Communication

doi: 10.3390/molecules26061651

Figure Lengend Snippet: Effect of HY7714 EPS on ECM modulation in HS68 cells. ( A ) The intracellular level of matrix metalloproteinase1 (MMP1) in HS68 cells treated with HY7714 EPS was measured using an MMP1 ELISA kit. ( B , C ) Relative mRNA levels of MMP1 and HAS1 in HS68 cells were calculated by qPCR and normalized against GAPDH. ( D ) Western blotting for MMP1 and COLa1 in HS68 cells, and quantification of band density. Data are expressed as means ± SD ( n = 4), and values labeled with different letters are significantly different, p < 0.05 (a > b > c). CON, control cells.

Article Snippet: Cell culture medium was collected, and MMP1 was quantified using commercial ELISA/calorimetric assay kits (CUSABIO, Houston, TX, USA; CSB-E04672h).

Techniques: Enzyme-linked Immunosorbent Assay, Western Blot, Labeling

Effect of HY7714 EPS on protein levels of MMPs and intracellular hyaluronic acid (HA) in UVB-irradiated HS68 cells. ( A ) Relative levels of intracellular MMP1 in HS68 cells treated with HY7714 EPS were measured using an MMP1 ELISA kit. MMP1 production was amplified by pre-treatment with 100 ng/mL TNFα for 2 h. ( B ) Intracellular HA in UVB-exposed cells treated with HY7714 EPS was measured using an HA ELISA kit. ( C ) Western blotting for MMP1 and MMP13 in HS68 cells, and quantification of band density. Data are expressed as means ± SD ( n = 3), and values labeled with different letters are significantly different, p < 0.05 (a > b > c).

Journal: Molecules

Article Title: Exopolysaccharide from Lactobacillus plantarum HY7714 Protects against Skin Aging through Skin–Gut Axis Communication

doi: 10.3390/molecules26061651

Figure Lengend Snippet: Effect of HY7714 EPS on protein levels of MMPs and intracellular hyaluronic acid (HA) in UVB-irradiated HS68 cells. ( A ) Relative levels of intracellular MMP1 in HS68 cells treated with HY7714 EPS were measured using an MMP1 ELISA kit. MMP1 production was amplified by pre-treatment with 100 ng/mL TNFα for 2 h. ( B ) Intracellular HA in UVB-exposed cells treated with HY7714 EPS was measured using an HA ELISA kit. ( C ) Western blotting for MMP1 and MMP13 in HS68 cells, and quantification of band density. Data are expressed as means ± SD ( n = 3), and values labeled with different letters are significantly different, p < 0.05 (a > b > c).

Article Snippet: Cell culture medium was collected, and MMP1 was quantified using commercial ELISA/calorimetric assay kits (CUSABIO, Houston, TX, USA; CSB-E04672h).

Techniques: Irradiation, Enzyme-linked Immunosorbent Assay, Amplification, Western Blot, Labeling

hucMSC-exosomes inhibited intimal hyperplasia and luminal stenosis in arterialized vein grafts. a Representative ultrasound images of vein grafts from the PBS group (left panel) and exosome group (right panel). Quantification of the luminal diameter ( b ) and peak-systolic velocity ( c ) in vein grafts. d Histologic images of haematoxylin and eosin staining (HE) staining in vein grafts from the normal vein group (left panel), PBS group (middle panel), and exosome group (right panel). e Quantification of the neointimal thickness in vein grafts. f Immunohistochemical staining of matrix metalloproteinase 2 (MMP-2) in vein grafts from the PBS group (left panel) and exosome group (right panel). g Immunohistochemical staining of matrix metalloproteinase 9 (MMP-9) in vein grafts from the PBS group (left panel) and exosome group (right panel). h Immunohistochemical staining of proliferating cell nuclear antigen (PCNA) in vein grafts from the PBS group (left panel) and exosome group (right panel). i Quantitative analysis of PCNA-positive index in vein grafts. The PCNA-positive index was quantified as the percentage of total nuclei in the neointima. Scale bar is 200 μm in panels d , f , g , and h . The results are presented as the mean ± SD, n = 6 for each group. An asterisk represents statistically significant difference compared with the PBS group ( P < 0.05). Number sign represents statistically significant difference compared with the normal vein group ( P < 0.05)

Journal: Stem Cell Research & Therapy

Article Title: Exosomes derived from human umbilical cord mesenchymal stem cells inhibit vein graft intimal hyperplasia and accelerate reendothelialization by enhancing endothelial function

doi: 10.1186/s13287-020-01639-1

Figure Lengend Snippet: hucMSC-exosomes inhibited intimal hyperplasia and luminal stenosis in arterialized vein grafts. a Representative ultrasound images of vein grafts from the PBS group (left panel) and exosome group (right panel). Quantification of the luminal diameter ( b ) and peak-systolic velocity ( c ) in vein grafts. d Histologic images of haematoxylin and eosin staining (HE) staining in vein grafts from the normal vein group (left panel), PBS group (middle panel), and exosome group (right panel). e Quantification of the neointimal thickness in vein grafts. f Immunohistochemical staining of matrix metalloproteinase 2 (MMP-2) in vein grafts from the PBS group (left panel) and exosome group (right panel). g Immunohistochemical staining of matrix metalloproteinase 9 (MMP-9) in vein grafts from the PBS group (left panel) and exosome group (right panel). h Immunohistochemical staining of proliferating cell nuclear antigen (PCNA) in vein grafts from the PBS group (left panel) and exosome group (right panel). i Quantitative analysis of PCNA-positive index in vein grafts. The PCNA-positive index was quantified as the percentage of total nuclei in the neointima. Scale bar is 200 μm in panels d , f , g , and h . The results are presented as the mean ± SD, n = 6 for each group. An asterisk represents statistically significant difference compared with the PBS group ( P < 0.05). Number sign represents statistically significant difference compared with the normal vein group ( P < 0.05)

Article Snippet: Matrix metalloproteinase-2 (MMP2, 1:200, Proteintech, Wuhan, China) and matrix metalloproteinase-9 (MMP9, 1:200, Proteintech) and proliferating cell nuclear antigen (PCNA, 1:10000, Abcam, UK) immunohistochemical staining was carried out using SP-9100 Detection Kits to figure out neointimal formation in the vein grafts.

Techniques: Staining, Immunohistochemical staining