mfap Search Results


93
Proteintech agtr1
Agtr1, 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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Adipogen antibodies specific human mfap-4
Quantitative RT-PCR analysis of <t>MFAP-4</t> in human skin was performed. (a) The expression of MFAP-4 in xenografted human skin after repeated UVB irradiations with 1 to 2 MED for 6 wks was normalized to the expression of the ribosomal protein, RPLP0 , and the relative value compared to the non-irradiated control is shown. (b) MFAP-4 expression in human skin punch biopsies at the ventral area of upper arms from young (twenties) and old (fifties) Caucasian women. The results normalized by RPLP0 expression are presented. Values reported represent means ± SD. *p<0.05, **p<0.01.
Antibodies Specific Human Mfap 4, supplied by Adipogen, 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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90
Crown Bioscience ct26 cell line
Quantitative RT-PCR analysis of <t>MFAP-4</t> in human skin was performed. (a) The expression of MFAP-4 in xenografted human skin after repeated UVB irradiations with 1 to 2 MED for 6 wks was normalized to the expression of the ribosomal protein, RPLP0 , and the relative value compared to the non-irradiated control is shown. (b) MFAP-4 expression in human skin punch biopsies at the ventral area of upper arms from young (twenties) and old (fifties) Caucasian women. The results normalized by RPLP0 expression are presented. Values reported represent means ± SD. *p<0.05, **p<0.01.
Ct26 Cell Line, supplied by Crown Bioscience, 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
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90
Merck & Co mouse anti- mfap- 4 antibody
Quantitative RT-PCR analysis of <t>MFAP-4</t> in human skin was performed. (a) The expression of MFAP-4 in xenografted human skin after repeated UVB irradiations with 1 to 2 MED for 6 wks was normalized to the expression of the ribosomal protein, RPLP0 , and the relative value compared to the non-irradiated control is shown. (b) MFAP-4 expression in human skin punch biopsies at the ventral area of upper arms from young (twenties) and old (fifties) Caucasian women. The results normalized by RPLP0 expression are presented. Values reported represent means ± SD. *p<0.05, **p<0.01.
Mouse Anti Mfap 4 Antibody, supplied by Merck & Co, 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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90
Kao Corporation microfibril- protein 4 (mfap- 4
Quantitative RT-PCR analysis of <t>MFAP-4</t> in human skin was performed. (a) The expression of MFAP-4 in xenografted human skin after repeated UVB irradiations with 1 to 2 MED for 6 wks was normalized to the expression of the ribosomal protein, RPLP0 , and the relative value compared to the non-irradiated control is shown. (b) MFAP-4 expression in human skin punch biopsies at the ventral area of upper arms from young (twenties) and old (fifties) Caucasian women. The results normalized by RPLP0 expression are presented. Values reported represent means ± SD. *p<0.05, **p<0.01.
Microfibril Protein 4 (Mfap 4, supplied by Kao Corporation, 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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90
NanoVector amphiphilic polymer (mfap)
Quantitative RT-PCR analysis of <t>MFAP-4</t> in human skin was performed. (a) The expression of MFAP-4 in xenografted human skin after repeated UVB irradiations with 1 to 2 MED for 6 wks was normalized to the expression of the ribosomal protein, RPLP0 , and the relative value compared to the non-irradiated control is shown. (b) MFAP-4 expression in human skin punch biopsies at the ventral area of upper arms from young (twenties) and old (fifties) Caucasian women. The results normalized by RPLP0 expression are presented. Values reported represent means ± SD. *p<0.05, **p<0.01.
Amphiphilic Polymer (Mfap), supplied by NanoVector, 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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90
Georg Thieme Verlag KG mfap (9)
Quantitative RT-PCR analysis of <t>MFAP-4</t> in human skin was performed. (a) The expression of MFAP-4 in xenografted human skin after repeated UVB irradiations with 1 to 2 MED for 6 wks was normalized to the expression of the ribosomal protein, RPLP0 , and the relative value compared to the non-irradiated control is shown. (b) MFAP-4 expression in human skin punch biopsies at the ventral area of upper arms from young (twenties) and old (fifties) Caucasian women. The results normalized by RPLP0 expression are presented. Values reported represent means ± SD. *p<0.05, **p<0.01.
Mfap (9), supplied by Georg Thieme Verlag KG, 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


Quantitative RT-PCR analysis of MFAP-4 in human skin was performed. (a) The expression of MFAP-4 in xenografted human skin after repeated UVB irradiations with 1 to 2 MED for 6 wks was normalized to the expression of the ribosomal protein, RPLP0 , and the relative value compared to the non-irradiated control is shown. (b) MFAP-4 expression in human skin punch biopsies at the ventral area of upper arms from young (twenties) and old (fifties) Caucasian women. The results normalized by RPLP0 expression are presented. Values reported represent means ± SD. *p<0.05, **p<0.01.

Journal: Scientific Reports

Article Title: Essential role of microfibrillar-associated protein 4 in human cutaneous homeostasis and in its photoprotection

doi: 10.1038/srep00164

Figure Lengend Snippet: Quantitative RT-PCR analysis of MFAP-4 in human skin was performed. (a) The expression of MFAP-4 in xenografted human skin after repeated UVB irradiations with 1 to 2 MED for 6 wks was normalized to the expression of the ribosomal protein, RPLP0 , and the relative value compared to the non-irradiated control is shown. (b) MFAP-4 expression in human skin punch biopsies at the ventral area of upper arms from young (twenties) and old (fifties) Caucasian women. The results normalized by RPLP0 expression are presented. Values reported represent means ± SD. *p<0.05, **p<0.01.

Article Snippet: Samples were transferred to PVDF membranes (Bio-Rad Laboratories) and were incubated with antibodies specific for human MFAP-4 (AdipoGen, Incheon, Korea), human collagen I (United States Biological, Swampscott, MA), human MMP-1 (AbD Serotec, Oxford, UK), human MMP-12 (Millipore), human fibrillin-1 (Elastin Products Company) or human β-actin (Sigma).

Techniques: Quantitative RT-PCR, Expressing, Irradiation

Immunohistological staining with rabbit polyclonal anti-human MFAP-4 and normal rabbit control IgG was conducted on paraffin embedded sections of biopsied skin specimens. They were from the ventral upper arm of the donors in their thirties and sixties, or from the dorsal lower arms of the donors in their sixties. Scale bars = 50 μm.

Journal: Scientific Reports

Article Title: Essential role of microfibrillar-associated protein 4 in human cutaneous homeostasis and in its photoprotection

doi: 10.1038/srep00164

Figure Lengend Snippet: Immunohistological staining with rabbit polyclonal anti-human MFAP-4 and normal rabbit control IgG was conducted on paraffin embedded sections of biopsied skin specimens. They were from the ventral upper arm of the donors in their thirties and sixties, or from the dorsal lower arms of the donors in their sixties. Scale bars = 50 μm.

Article Snippet: Samples were transferred to PVDF membranes (Bio-Rad Laboratories) and were incubated with antibodies specific for human MFAP-4 (AdipoGen, Incheon, Korea), human collagen I (United States Biological, Swampscott, MA), human MMP-1 (AbD Serotec, Oxford, UK), human MMP-12 (Millipore), human fibrillin-1 (Elastin Products Company) or human β-actin (Sigma).

Techniques: Staining

(a) Lentiviral vectors to over-express MFAP-4 or a control reporter gene were intradermally administered into human xenografted skin twice with a week interval, subjected to continuous UVB irradiations at 1 to 2 MED for 8 wks as indicated. (b) Immunohistological staining with rabbit polyclonal anti-human MFAP-4 and normal rabbit control IgG was performed on paraffin embedded sections from non-exposed skin with a control reporter gene over-expression, a control reporter gene-transduced skin with UVB irradiation for 8 wks and MFAP-4 -over-expressed skin with repetitive UVB irradiation for 8 wks. Scale bars = 100 μm. (c) En face representative images of xenografted skin were captured at 0 (before the lentiviral administration), 6 (before the UVB irradiation), 10, 14 (just after the completion of continuous UVB exposures) and 20 wks (6 wks after the final UVB irradiation) using a hand-held microscope. The non-UVB irradiated control with a control reporter gene over-expression, the long-term UVB-irradiated skin with a control reporter gene over-expression and MFAP-4 -over-expressed skin with repetitive UVB exposure are shown at the top, middle and bottom, respectively. Scale bars = 3 mm. (d) Skin profilometry of replicas was utilized to evaluate surface roughness using arithmetic mean roughness (Sa) and mean peak to valley height (Sz) at the indicated time points. The values reported represent means ± SD. *p<0.05, **p<0.01. 1; vs the values of the UVB-irradiated control with a control reporter gene over-expression. 2; vs the values of the non-irradiated control with a control reporter gene over-expression. (e) Skin elasticity was evaluated using a Cutometer SEM575 at the same time points as the assessments of skin surface roughness. Ur/Ue represents pure elasticity ignoring creep. The values reported represent means ± SD. *p<0.05. 1; vs the values of the UVB-irradiated control with a control reporter gene over-expression.

Journal: Scientific Reports

Article Title: Essential role of microfibrillar-associated protein 4 in human cutaneous homeostasis and in its photoprotection

doi: 10.1038/srep00164

Figure Lengend Snippet: (a) Lentiviral vectors to over-express MFAP-4 or a control reporter gene were intradermally administered into human xenografted skin twice with a week interval, subjected to continuous UVB irradiations at 1 to 2 MED for 8 wks as indicated. (b) Immunohistological staining with rabbit polyclonal anti-human MFAP-4 and normal rabbit control IgG was performed on paraffin embedded sections from non-exposed skin with a control reporter gene over-expression, a control reporter gene-transduced skin with UVB irradiation for 8 wks and MFAP-4 -over-expressed skin with repetitive UVB irradiation for 8 wks. Scale bars = 100 μm. (c) En face representative images of xenografted skin were captured at 0 (before the lentiviral administration), 6 (before the UVB irradiation), 10, 14 (just after the completion of continuous UVB exposures) and 20 wks (6 wks after the final UVB irradiation) using a hand-held microscope. The non-UVB irradiated control with a control reporter gene over-expression, the long-term UVB-irradiated skin with a control reporter gene over-expression and MFAP-4 -over-expressed skin with repetitive UVB exposure are shown at the top, middle and bottom, respectively. Scale bars = 3 mm. (d) Skin profilometry of replicas was utilized to evaluate surface roughness using arithmetic mean roughness (Sa) and mean peak to valley height (Sz) at the indicated time points. The values reported represent means ± SD. *p<0.05, **p<0.01. 1; vs the values of the UVB-irradiated control with a control reporter gene over-expression. 2; vs the values of the non-irradiated control with a control reporter gene over-expression. (e) Skin elasticity was evaluated using a Cutometer SEM575 at the same time points as the assessments of skin surface roughness. Ur/Ue represents pure elasticity ignoring creep. The values reported represent means ± SD. *p<0.05. 1; vs the values of the UVB-irradiated control with a control reporter gene over-expression.

Article Snippet: Samples were transferred to PVDF membranes (Bio-Rad Laboratories) and were incubated with antibodies specific for human MFAP-4 (AdipoGen, Incheon, Korea), human collagen I (United States Biological, Swampscott, MA), human MMP-1 (AbD Serotec, Oxford, UK), human MMP-12 (Millipore), human fibrillin-1 (Elastin Products Company) or human β-actin (Sigma).

Techniques: Staining, Over Expression, Irradiation, Microscopy

(a) Luna staining was performed to evaluate the role of MFAP-4 in the protection of elastic fibers using paraffin-embedded sections from non-exposed skin with a control reporter gene over-expression, a control reporter gene-transduced skin with UVB irradiation for 8 wks and MFAP-4 -over-expressed skin with repetitive UVB irradiation for 8 wks. Scale bars = 100 μm. (b) MMP-12 activities in xenografted human skins treated with lentiviral vectors encoding a control reporter gene with or without UVB irradiation for 8 wks and UVB-exposed skin with MFAP-4 over-expression were evaluated using fluorescent-tagged MMP-12 substrate as detailed in the Methods. The values reported represent means ± SD. **p<0.01; vs the value in UVB-exposed skin with a control reporter gene over-expression.

Journal: Scientific Reports

Article Title: Essential role of microfibrillar-associated protein 4 in human cutaneous homeostasis and in its photoprotection

doi: 10.1038/srep00164

Figure Lengend Snippet: (a) Luna staining was performed to evaluate the role of MFAP-4 in the protection of elastic fibers using paraffin-embedded sections from non-exposed skin with a control reporter gene over-expression, a control reporter gene-transduced skin with UVB irradiation for 8 wks and MFAP-4 -over-expressed skin with repetitive UVB irradiation for 8 wks. Scale bars = 100 μm. (b) MMP-12 activities in xenografted human skins treated with lentiviral vectors encoding a control reporter gene with or without UVB irradiation for 8 wks and UVB-exposed skin with MFAP-4 over-expression were evaluated using fluorescent-tagged MMP-12 substrate as detailed in the Methods. The values reported represent means ± SD. **p<0.01; vs the value in UVB-exposed skin with a control reporter gene over-expression.

Article Snippet: Samples were transferred to PVDF membranes (Bio-Rad Laboratories) and were incubated with antibodies specific for human MFAP-4 (AdipoGen, Incheon, Korea), human collagen I (United States Biological, Swampscott, MA), human MMP-1 (AbD Serotec, Oxford, UK), human MMP-12 (Millipore), human fibrillin-1 (Elastin Products Company) or human β-actin (Sigma).

Techniques: Staining, Over Expression, Irradiation

NHDFs were transfected with siRNAs for non-specific sequences (Control) or MFAP-4 twice during the culture for 8 days. Control siRNA-transfected cells were treated with or without 10 nM human recombinant MFAP-4 during the culture. (a) Quantitative RT-PCR analysis was performed with MFAP-4 -specific Taq Man Gene Expression Assays after the reverse transcription of total RNAs from cultured NHDFs. The mRNA expression of the target gene was normalized against the expression of GAPDH mRNA and is relatively presented. The values reported represent means ± SD. ***p<0.001. (b) Western blotting analysis with antibodies specific for MFAP-4 or fibrillin-1 was conducted to confirm the impact of MFAP-4 silencing on their protein abundance using the supernatants from cultured NHDFs. (c) Immunofluorescence staining was performed with an anti-human tropoelastin antibody (green) and an anti-human fibrillin-1 antibody (red). Nuclear staining (DAPI) and merged images are also shown in the diagram. Scale bars = 50 μm. (d) Quantitative RT-PCR analysis of the MMP-12 mRNA expression in cultured NHDFs was performed as described in the legend of . The values reported represent means ± SD. ***p<0.001, **p<0.01. (e) Western blotting analysis with an anti-human MMP-12 antibody was performed for the supernatants from cultured NHDFs. The obtained bands of the active form of MMP-12 were analyzed using a densitometer and the values in the graph are represented relatively. The values reported represent means ± SD. *p<0.05. (f) NHDFs were cultured for 8 days with or without 20 nM human recombinant MFAP-4 during the culture in FBS-free medium. Immunofluorescence staining was performed as described in the legend of . Scale bars = 50 μm.

Journal: Scientific Reports

Article Title: Essential role of microfibrillar-associated protein 4 in human cutaneous homeostasis and in its photoprotection

doi: 10.1038/srep00164

Figure Lengend Snippet: NHDFs were transfected with siRNAs for non-specific sequences (Control) or MFAP-4 twice during the culture for 8 days. Control siRNA-transfected cells were treated with or without 10 nM human recombinant MFAP-4 during the culture. (a) Quantitative RT-PCR analysis was performed with MFAP-4 -specific Taq Man Gene Expression Assays after the reverse transcription of total RNAs from cultured NHDFs. The mRNA expression of the target gene was normalized against the expression of GAPDH mRNA and is relatively presented. The values reported represent means ± SD. ***p<0.001. (b) Western blotting analysis with antibodies specific for MFAP-4 or fibrillin-1 was conducted to confirm the impact of MFAP-4 silencing on their protein abundance using the supernatants from cultured NHDFs. (c) Immunofluorescence staining was performed with an anti-human tropoelastin antibody (green) and an anti-human fibrillin-1 antibody (red). Nuclear staining (DAPI) and merged images are also shown in the diagram. Scale bars = 50 μm. (d) Quantitative RT-PCR analysis of the MMP-12 mRNA expression in cultured NHDFs was performed as described in the legend of . The values reported represent means ± SD. ***p<0.001, **p<0.01. (e) Western blotting analysis with an anti-human MMP-12 antibody was performed for the supernatants from cultured NHDFs. The obtained bands of the active form of MMP-12 were analyzed using a densitometer and the values in the graph are represented relatively. The values reported represent means ± SD. *p<0.05. (f) NHDFs were cultured for 8 days with or without 20 nM human recombinant MFAP-4 during the culture in FBS-free medium. Immunofluorescence staining was performed as described in the legend of . Scale bars = 50 μm.

Article Snippet: Samples were transferred to PVDF membranes (Bio-Rad Laboratories) and were incubated with antibodies specific for human MFAP-4 (AdipoGen, Incheon, Korea), human collagen I (United States Biological, Swampscott, MA), human MMP-1 (AbD Serotec, Oxford, UK), human MMP-12 (Millipore), human fibrillin-1 (Elastin Products Company) or human β-actin (Sigma).

Techniques: Transfection, Recombinant, Quantitative RT-PCR, Expressing, Cell Culture, Western Blot, Immunofluorescence, Staining

(a) Concentrated supernatants from NHDFs cultured for 8 days were immunoprecipitated with an anti-MFAP-4 antibody or normal rabbit IgG. Immunoprecipitants were analyzed by Western blotting with an anti-fibrillin-1 antibody. (b) NHDFs were transfected with siRNAs for non-specific sequences (Control) or MFAP-4 twice during the culture for 8 days, followed by immunofluorescence staining with an anti-human MFAP-4 antibody (green) and an anti-human fibrillin-1 antibody (red). Nuclear staining (DAPI) and merged images are also shown. Scale bars = 50 μm.

Journal: Scientific Reports

Article Title: Essential role of microfibrillar-associated protein 4 in human cutaneous homeostasis and in its photoprotection

doi: 10.1038/srep00164

Figure Lengend Snippet: (a) Concentrated supernatants from NHDFs cultured for 8 days were immunoprecipitated with an anti-MFAP-4 antibody or normal rabbit IgG. Immunoprecipitants were analyzed by Western blotting with an anti-fibrillin-1 antibody. (b) NHDFs were transfected with siRNAs for non-specific sequences (Control) or MFAP-4 twice during the culture for 8 days, followed by immunofluorescence staining with an anti-human MFAP-4 antibody (green) and an anti-human fibrillin-1 antibody (red). Nuclear staining (DAPI) and merged images are also shown. Scale bars = 50 μm.

Article Snippet: Samples were transferred to PVDF membranes (Bio-Rad Laboratories) and were incubated with antibodies specific for human MFAP-4 (AdipoGen, Incheon, Korea), human collagen I (United States Biological, Swampscott, MA), human MMP-1 (AbD Serotec, Oxford, UK), human MMP-12 (Millipore), human fibrillin-1 (Elastin Products Company) or human β-actin (Sigma).

Techniques: Cell Culture, Immunoprecipitation, Western Blot, Transfection, Immunofluorescence, Staining

(a) Immunohistochemical analysis with a rabbit anti-human collagen I antibody or a non-specific control rabbit IgG was carried out using paraffin embedded sections from the xenografted skin treated with a lentiviral vector encoding a control reporter gene with or without continuous UVB irradiation for 8 wks and using xenografted skin over-expressing MFAP-4 with UVB exposure for 8 wks. Scale bars = 100 μm. (b) Western blotting analysis with an anti-human collagen I or an anti-human β-actin antibody to assess the protein levels of collagen I in xenografted skin treated with lentiviral vectors encoding a control reporter gene or MFAP-4 before and after UVB exposure for 4 wks. (c) NHDFs were transfected with siRNAs for non-specific sequences (Control) or MFAP-4 twice during the culture for 8 days. Control siRNA-transfected cells were treated with or without 10 nM human recombinant MFAP-4 during the culture. Quantitative RT-PCR analysis of the MMP-1 mRNA expression in cultured NHDFs was performed as described in the legend of . The values reported represent means ± SD. ***p<0.001. (d) Western blotting analysis with an anti-human MMP-1 antibody was conducted for supernatants from cultured NHDFs treated as described in . The obtained bands of the active form of MMP-1 were analyzed using a densitometer and the values in the graph are represented relatively. The values reported represent means ±SD. **p<0.01, *p<0.05.

Journal: Scientific Reports

Article Title: Essential role of microfibrillar-associated protein 4 in human cutaneous homeostasis and in its photoprotection

doi: 10.1038/srep00164

Figure Lengend Snippet: (a) Immunohistochemical analysis with a rabbit anti-human collagen I antibody or a non-specific control rabbit IgG was carried out using paraffin embedded sections from the xenografted skin treated with a lentiviral vector encoding a control reporter gene with or without continuous UVB irradiation for 8 wks and using xenografted skin over-expressing MFAP-4 with UVB exposure for 8 wks. Scale bars = 100 μm. (b) Western blotting analysis with an anti-human collagen I or an anti-human β-actin antibody to assess the protein levels of collagen I in xenografted skin treated with lentiviral vectors encoding a control reporter gene or MFAP-4 before and after UVB exposure for 4 wks. (c) NHDFs were transfected with siRNAs for non-specific sequences (Control) or MFAP-4 twice during the culture for 8 days. Control siRNA-transfected cells were treated with or without 10 nM human recombinant MFAP-4 during the culture. Quantitative RT-PCR analysis of the MMP-1 mRNA expression in cultured NHDFs was performed as described in the legend of . The values reported represent means ± SD. ***p<0.001. (d) Western blotting analysis with an anti-human MMP-1 antibody was conducted for supernatants from cultured NHDFs treated as described in . The obtained bands of the active form of MMP-1 were analyzed using a densitometer and the values in the graph are represented relatively. The values reported represent means ±SD. **p<0.01, *p<0.05.

Article Snippet: Samples were transferred to PVDF membranes (Bio-Rad Laboratories) and were incubated with antibodies specific for human MFAP-4 (AdipoGen, Incheon, Korea), human collagen I (United States Biological, Swampscott, MA), human MMP-1 (AbD Serotec, Oxford, UK), human MMP-12 (Millipore), human fibrillin-1 (Elastin Products Company) or human β-actin (Sigma).

Techniques: Immunohistochemical staining, Plasmid Preparation, Irradiation, Expressing, Western Blot, Transfection, Recombinant, Quantitative RT-PCR, Cell Culture

(a) Secreted MFAP-4 and fibrillin-1 interact directly, resulting in the assembly of microfibrils under normal conditions. Tropoelastins assembled with LOX recruited by fibulin-4 are subsequently cross-linked with microfibrils for the formation of complete mature elastic fibers. (b) In the absence of MFAP-4, fibrillin-1 cannot be assembled or matured for the formation of microfibrils. Tropoelastins are never cross-linked due to the failure of microfibril formation.

Journal: Scientific Reports

Article Title: Essential role of microfibrillar-associated protein 4 in human cutaneous homeostasis and in its photoprotection

doi: 10.1038/srep00164

Figure Lengend Snippet: (a) Secreted MFAP-4 and fibrillin-1 interact directly, resulting in the assembly of microfibrils under normal conditions. Tropoelastins assembled with LOX recruited by fibulin-4 are subsequently cross-linked with microfibrils for the formation of complete mature elastic fibers. (b) In the absence of MFAP-4, fibrillin-1 cannot be assembled or matured for the formation of microfibrils. Tropoelastins are never cross-linked due to the failure of microfibril formation.

Article Snippet: Samples were transferred to PVDF membranes (Bio-Rad Laboratories) and were incubated with antibodies specific for human MFAP-4 (AdipoGen, Incheon, Korea), human collagen I (United States Biological, Swampscott, MA), human MMP-1 (AbD Serotec, Oxford, UK), human MMP-12 (Millipore), human fibrillin-1 (Elastin Products Company) or human β-actin (Sigma).

Techniques: