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Mouse Monoclonal Anticollagen Pro Type I, supplied by Developmental Studies Hybridoma Bank, 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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Thermo Fisher mouse anti collagen type i primary antibody
Results of antioxidant <t>and</t> <t>pro-collagen</t> effects of CA-PDENs. (A) Graphical depiction of DPPH radical scavenging activity of CA-PDENs and vitamin C within the concentration of 6.25-400 µg/mL, data are presented as mean ± standard deviation (n = 3). (B) Fluorescence intensity in UVB-induced 1BR3 cells represents the level of intracellular ROS after CA-PDENs treatment for 24 hours; data are presented as mean ± standard deviation (n = 3). *p < 0.05, **p-value < 0.01 vs. negative control. (C) Confocal microscopy images showing collagen <t>type</t> <t>I</t> expression in 1BR3 cells after 6 hours of CA-PDENs incubation at the concentrations of 40 and 100 µg/mL (200× magnification). Nuclei were stained with DAPI (blue), while collagen type 1 was labeled with Alexa Fluor 647 (red). Merged images show the localization of collagen type 1 expression in the cytoplasmic region surrounding the nuclei. (D) Collagen type I levels in UVB-induced 1BR3 cells followed by CA-PDENs incubation at 40 and 100 µg/mL for 48 hours, data are presented as mean ± standard deviation (n = 3). **p-value < 0.01 vs. control. Abbreviations: CA-PDENs, Centella asiatica -derived exosome-like nanovesicles; DPPH, 2,2-diphenyl-1-picrylhydrazyl; ROS, reactive oxygen species; UVB, ultraviolet B; DAPI, 4′,6-diamidino-2-phenylindole.
Mouse Anti Collagen Type I Primary Antibody, 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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Proteintech mouse col1 mab
Results of antioxidant <t>and</t> <t>pro-collagen</t> effects of CA-PDENs. (A) Graphical depiction of DPPH radical scavenging activity of CA-PDENs and vitamin C within the concentration of 6.25-400 µg/mL, data are presented as mean ± standard deviation (n = 3). (B) Fluorescence intensity in UVB-induced 1BR3 cells represents the level of intracellular ROS after CA-PDENs treatment for 24 hours; data are presented as mean ± standard deviation (n = 3). *p < 0.05, **p-value < 0.01 vs. negative control. (C) Confocal microscopy images showing collagen <t>type</t> <t>I</t> expression in 1BR3 cells after 6 hours of CA-PDENs incubation at the concentrations of 40 and 100 µg/mL (200× magnification). Nuclei were stained with DAPI (blue), while collagen type 1 was labeled with Alexa Fluor 647 (red). Merged images show the localization of collagen type 1 expression in the cytoplasmic region surrounding the nuclei. (D) Collagen type I levels in UVB-induced 1BR3 cells followed by CA-PDENs incubation at 40 and 100 µg/mL for 48 hours, data are presented as mean ± standard deviation (n = 3). **p-value < 0.01 vs. control. Abbreviations: CA-PDENs, Centella asiatica -derived exosome-like nanovesicles; DPPH, 2,2-diphenyl-1-picrylhydrazyl; ROS, reactive oxygen species; UVB, ultraviolet B; DAPI, 4′,6-diamidino-2-phenylindole.
Mouse Col1 Mab, supplied by Proteintech, 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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Proteintech rabbit anti mouse col
Results of antioxidant <t>and</t> <t>pro-collagen</t> effects of CA-PDENs. (A) Graphical depiction of DPPH radical scavenging activity of CA-PDENs and vitamin C within the concentration of 6.25-400 µg/mL, data are presented as mean ± standard deviation (n = 3). (B) Fluorescence intensity in UVB-induced 1BR3 cells represents the level of intracellular ROS after CA-PDENs treatment for 24 hours; data are presented as mean ± standard deviation (n = 3). *p < 0.05, **p-value < 0.01 vs. negative control. (C) Confocal microscopy images showing collagen <t>type</t> <t>I</t> expression in 1BR3 cells after 6 hours of CA-PDENs incubation at the concentrations of 40 and 100 µg/mL (200× magnification). Nuclei were stained with DAPI (blue), while collagen type 1 was labeled with Alexa Fluor 647 (red). Merged images show the localization of collagen type 1 expression in the cytoplasmic region surrounding the nuclei. (D) Collagen type I levels in UVB-induced 1BR3 cells followed by CA-PDENs incubation at 40 and 100 µg/mL for 48 hours, data are presented as mean ± standard deviation (n = 3). **p-value < 0.01 vs. control. Abbreviations: CA-PDENs, Centella asiatica -derived exosome-like nanovesicles; DPPH, 2,2-diphenyl-1-picrylhydrazyl; ROS, reactive oxygen species; UVB, ultraviolet B; DAPI, 4′,6-diamidino-2-phenylindole.
Rabbit Anti Mouse Col, supplied by Proteintech, 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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Novus Biologicals mouse anti collagen type i
SDS-PAGE (A) and densitometry analysis (B) of collagen <t>type</t> <t>I</t> deposition of human BMSCs after 5 days in culture without (−) and with (+) MMC. # indicates significant ( p < 0.05) difference. N = 3.
Mouse Anti Collagen Type I, supplied by Novus Biologicals, 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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SDS-PAGE (A) and densitometry analysis (B) of collagen <t>type</t> <t>I</t> deposition of human BMSCs after 5 days in culture without (−) and with (+) MMC. # indicates significant ( p < 0.05) difference. N = 3.
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SDS-PAGE (A) and densitometry analysis (B) of collagen <t>type</t> <t>I</t> deposition of human BMSCs after 5 days in culture without (−) and with (+) MMC. # indicates significant ( p < 0.05) difference. N = 3.
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Proteintech collagen type i mouse monoclonal antibody
SDS-PAGE (A) and densitometry analysis (B) of collagen <t>type</t> <t>I</t> deposition of human BMSCs after 5 days in culture without (−) and with (+) MMC. # indicates significant ( p < 0.05) difference. N = 3.
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Proteintech mouse anti col1a1
SDS-PAGE (A) and densitometry analysis (B) of collagen <t>type</t> <t>I</t> deposition of human BMSCs after 5 days in culture without (−) and with (+) MMC. # indicates significant ( p < 0.05) difference. N = 3.
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Results of antioxidant and pro-collagen effects of CA-PDENs. (A) Graphical depiction of DPPH radical scavenging activity of CA-PDENs and vitamin C within the concentration of 6.25-400 µg/mL, data are presented as mean ± standard deviation (n = 3). (B) Fluorescence intensity in UVB-induced 1BR3 cells represents the level of intracellular ROS after CA-PDENs treatment for 24 hours; data are presented as mean ± standard deviation (n = 3). *p < 0.05, **p-value < 0.01 vs. negative control. (C) Confocal microscopy images showing collagen type I expression in 1BR3 cells after 6 hours of CA-PDENs incubation at the concentrations of 40 and 100 µg/mL (200× magnification). Nuclei were stained with DAPI (blue), while collagen type 1 was labeled with Alexa Fluor 647 (red). Merged images show the localization of collagen type 1 expression in the cytoplasmic region surrounding the nuclei. (D) Collagen type I levels in UVB-induced 1BR3 cells followed by CA-PDENs incubation at 40 and 100 µg/mL for 48 hours, data are presented as mean ± standard deviation (n = 3). **p-value < 0.01 vs. control. Abbreviations: CA-PDENs, Centella asiatica -derived exosome-like nanovesicles; DPPH, 2,2-diphenyl-1-picrylhydrazyl; ROS, reactive oxygen species; UVB, ultraviolet B; DAPI, 4′,6-diamidino-2-phenylindole.

Journal: Future Science OA

Article Title: The potential of plant-derived exosome-like nanovesicles from Centella asiatica leaves (CA-PDENs) for anti-inflammation and prevention of UVB-induced photoaging

doi: 10.1080/20565623.2026.2654777

Figure Lengend Snippet: Results of antioxidant and pro-collagen effects of CA-PDENs. (A) Graphical depiction of DPPH radical scavenging activity of CA-PDENs and vitamin C within the concentration of 6.25-400 µg/mL, data are presented as mean ± standard deviation (n = 3). (B) Fluorescence intensity in UVB-induced 1BR3 cells represents the level of intracellular ROS after CA-PDENs treatment for 24 hours; data are presented as mean ± standard deviation (n = 3). *p < 0.05, **p-value < 0.01 vs. negative control. (C) Confocal microscopy images showing collagen type I expression in 1BR3 cells after 6 hours of CA-PDENs incubation at the concentrations of 40 and 100 µg/mL (200× magnification). Nuclei were stained with DAPI (blue), while collagen type 1 was labeled with Alexa Fluor 647 (red). Merged images show the localization of collagen type 1 expression in the cytoplasmic region surrounding the nuclei. (D) Collagen type I levels in UVB-induced 1BR3 cells followed by CA-PDENs incubation at 40 and 100 µg/mL for 48 hours, data are presented as mean ± standard deviation (n = 3). **p-value < 0.01 vs. control. Abbreviations: CA-PDENs, Centella asiatica -derived exosome-like nanovesicles; DPPH, 2,2-diphenyl-1-picrylhydrazyl; ROS, reactive oxygen species; UVB, ultraviolet B; DAPI, 4′,6-diamidino-2-phenylindole.

Article Snippet: Cells were incubated overnight at 4 °C with a mouse anti-collagen type I primary antibody (1:500 in 1% BSA; Invitrogen, USA), followed by incubation with an Alexa Fluor 647-conjugated goat anti-mouse IgG secondary antibody (1:500 in 1% BSA; Abcam, USA) for 60 minutes in the dark.

Techniques: Activity Assay, Concentration Assay, Standard Deviation, Fluorescence, Negative Control, Confocal Microscopy, Expressing, Incubation, Staining, Labeling, Control, Derivative Assay

SDS-PAGE (A) and densitometry analysis (B) of collagen type I deposition of human BMSCs after 5 days in culture without (−) and with (+) MMC. # indicates significant ( p < 0.05) difference. N = 3.

Journal: Science Progress

Article Title: A preliminary preclinical assessment of macromolecular crowding in tissue engineering

doi: 10.1177/00368504251406914

Figure Lengend Snippet: SDS-PAGE (A) and densitometry analysis (B) of collagen type I deposition of human BMSCs after 5 days in culture without (−) and with (+) MMC. # indicates significant ( p < 0.05) difference. N = 3.

Article Snippet: At day 5, collagen type I, collagen type III and collagen type IV deposition was quantified using established immunofluorescence protocols., In brief, cell layers were washed, fixed, blocked, incubated with mouse anti-collagen type I (NB600-408, Novus Biologicals, USA), rabbit anti-collagen type III (Ab7778, Abcam, Ireland) or rabbit anti-collagen type V (Ab7046, Abcam, Ireland) primary antibodies, washed, incubated with AlexaFluor ® 488 goat anti-rabbit (A11008, Invitrogen, Ireland) or AlexaFluor ® 488 goat anti-mouse (A10667, Invitrogen, Ireland) secondary antibodies, washed and stained with DAPI (Invitrogen, Ireland).

Techniques: SDS Page

Immunofluorescence (A) and normalised to cell number image intensity analysis (B) of collagen type I, collagen type III and collagen type IV deposition of human BMSCs after 5 days in culture without (−) and with (+) MMC. # indicates significant ( p < 0.05) difference. Scale bar: 100 μm. N = 4.

Journal: Science Progress

Article Title: A preliminary preclinical assessment of macromolecular crowding in tissue engineering

doi: 10.1177/00368504251406914

Figure Lengend Snippet: Immunofluorescence (A) and normalised to cell number image intensity analysis (B) of collagen type I, collagen type III and collagen type IV deposition of human BMSCs after 5 days in culture without (−) and with (+) MMC. # indicates significant ( p < 0.05) difference. Scale bar: 100 μm. N = 4.

Article Snippet: At day 5, collagen type I, collagen type III and collagen type IV deposition was quantified using established immunofluorescence protocols., In brief, cell layers were washed, fixed, blocked, incubated with mouse anti-collagen type I (NB600-408, Novus Biologicals, USA), rabbit anti-collagen type III (Ab7778, Abcam, Ireland) or rabbit anti-collagen type V (Ab7046, Abcam, Ireland) primary antibodies, washed, incubated with AlexaFluor ® 488 goat anti-rabbit (A11008, Invitrogen, Ireland) or AlexaFluor ® 488 goat anti-mouse (A10667, Invitrogen, Ireland) secondary antibodies, washed and stained with DAPI (Invitrogen, Ireland).

Techniques: Immunofluorescence