3-dimensional principal components analysis Search Results


90
QUALISYS LIMITED 3-d optical data
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Selleck Chemicals oti cells
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Enamine Ltd cyclopropyl 4 morpho linyl 2 3 dimethyl pyrido 4 3 d pyrimidin 4 3h one step
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Becton Dickinson 3-dimensional growth factor depleted matrigel
A. FGF-2 induced vascular sprouting in the aortic ring model. Hpse- KO and wt derived aortic rings were subjected to FGF-2 induced vascular sprouting for 6 days. The rings were then fixed, stained with 0.02% crystal violet and evaluated for vascular sprouting. A more extensive endothelial sprouting was noted in Hpse- KO derived rings (right panel) as compared to wt derived rings (left panel). B. <t>Matrigel</t> plug assay. Hpse- KO (lower panels) and wt (upper panels) mice were injected subcutaneously with 200 µl of growth factor <t>depleted</t> <t>Matrigel</t> supplemented with FGF-2 (80 ng/ml). Seven days later, the Matrigel plugs were excised and photographed, followed by homogenization and determination of hemoglobin content using Drabkin's reagent (right). A pronounced angiogenic response was noted in Hpse- KO vs. wt mice (55±7.18 mg/dl vs. 21±6.2 mg/dl; p≤0.0002, respectively).
3 Dimensional Growth Factor Depleted Matrigel, supplied by Becton Dickinson, 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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Thermo Fisher purelink rna mini kit
A. FGF-2 induced vascular sprouting in the aortic ring model. Hpse- KO and wt derived aortic rings were subjected to FGF-2 induced vascular sprouting for 6 days. The rings were then fixed, stained with 0.02% crystal violet and evaluated for vascular sprouting. A more extensive endothelial sprouting was noted in Hpse- KO derived rings (right panel) as compared to wt derived rings (left panel). B. <t>Matrigel</t> plug assay. Hpse- KO (lower panels) and wt (upper panels) mice were injected subcutaneously with 200 µl of growth factor <t>depleted</t> <t>Matrigel</t> supplemented with FGF-2 (80 ng/ml). Seven days later, the Matrigel plugs were excised and photographed, followed by homogenization and determination of hemoglobin content using Drabkin's reagent (right). A pronounced angiogenic response was noted in Hpse- KO vs. wt mice (55±7.18 mg/dl vs. 21±6.2 mg/dl; p≤0.0002, respectively).
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Corning Life Sciences puramatrix
a Self-assembling peptide RADA16 molecular model. The calculated peptide dimensions are ~6 nm long depending on end capping, 1.3 nm wide and 0.8 nm thick. b Model of thousands of individual peptides as a single nanofiber. c Trilion of individual peptides self-assemble into nanofiber scaffold as revealed by the SEM. Scale bar = 0.5 µm. <t>d</t> <t>RADA16-I</t> peptide nanofibers scaffold hydrogel with extremely high-water content (99.5–99.0%, w/v water). An image of nanofiber scaffolds hydrogel of RADA16-I at 1% (10 mg/ml), 99% water (image courtesy of 3-D Matrix). e Murine neural stem cells are embedded in the nanofiber scaffold. The diameter of nanofiber is in the similar diameter as the cell produced extracellular matrix . f Red blood cells are embedded in the natural fibrin. g Dense RADA16 nanofiber scaffold . Billions of layers of interwoven nanofibers tightly keep blood cells in place thus preventing from bleeding.
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MBF Bioscience stereoinvestigator software
a Self-assembling peptide RADA16 molecular model. The calculated peptide dimensions are ~6 nm long depending on end capping, 1.3 nm wide and 0.8 nm thick. b Model of thousands of individual peptides as a single nanofiber. c Trilion of individual peptides self-assemble into nanofiber scaffold as revealed by the SEM. Scale bar = 0.5 µm. <t>d</t> <t>RADA16-I</t> peptide nanofibers scaffold hydrogel with extremely high-water content (99.5–99.0%, w/v water). An image of nanofiber scaffolds hydrogel of RADA16-I at 1% (10 mg/ml), 99% water (image courtesy of 3-D Matrix). e Murine neural stem cells are embedded in the nanofiber scaffold. The diameter of nanofiber is in the similar diameter as the cell produced extracellular matrix . f Red blood cells are embedded in the natural fibrin. g Dense RADA16 nanofiber scaffold . Billions of layers of interwoven nanofibers tightly keep blood cells in place thus preventing from bleeding.
Stereoinvestigator Software, supplied by MBF 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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SCANCO USA INC evaluation software μct v1.6
a Self-assembling peptide RADA16 molecular model. The calculated peptide dimensions are ~6 nm long depending on end capping, 1.3 nm wide and 0.8 nm thick. b Model of thousands of individual peptides as a single nanofiber. c Trilion of individual peptides self-assemble into nanofiber scaffold as revealed by the SEM. Scale bar = 0.5 µm. <t>d</t> <t>RADA16-I</t> peptide nanofibers scaffold hydrogel with extremely high-water content (99.5–99.0%, w/v water). An image of nanofiber scaffolds hydrogel of RADA16-I at 1% (10 mg/ml), 99% water (image courtesy of 3-D Matrix). e Murine neural stem cells are embedded in the nanofiber scaffold. The diameter of nanofiber is in the similar diameter as the cell produced extracellular matrix . f Red blood cells are embedded in the natural fibrin. g Dense RADA16 nanofiber scaffold . Billions of layers of interwoven nanofibers tightly keep blood cells in place thus preventing from bleeding.
Evaluation Software μct V1.6, supplied by SCANCO USA 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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Average 90 stars, based on 1 article reviews
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Image Search Results


A. FGF-2 induced vascular sprouting in the aortic ring model. Hpse- KO and wt derived aortic rings were subjected to FGF-2 induced vascular sprouting for 6 days. The rings were then fixed, stained with 0.02% crystal violet and evaluated for vascular sprouting. A more extensive endothelial sprouting was noted in Hpse- KO derived rings (right panel) as compared to wt derived rings (left panel). B. Matrigel plug assay. Hpse- KO (lower panels) and wt (upper panels) mice were injected subcutaneously with 200 µl of growth factor depleted Matrigel supplemented with FGF-2 (80 ng/ml). Seven days later, the Matrigel plugs were excised and photographed, followed by homogenization and determination of hemoglobin content using Drabkin's reagent (right). A pronounced angiogenic response was noted in Hpse- KO vs. wt mice (55±7.18 mg/dl vs. 21±6.2 mg/dl; p≤0.0002, respectively).

Journal: PLoS ONE

Article Title: Newly Generated Heparanase Knock-Out Mice Unravel Co-Regulation of Heparanase and Matrix Metalloproteinases

doi: 10.1371/journal.pone.0005181

Figure Lengend Snippet: A. FGF-2 induced vascular sprouting in the aortic ring model. Hpse- KO and wt derived aortic rings were subjected to FGF-2 induced vascular sprouting for 6 days. The rings were then fixed, stained with 0.02% crystal violet and evaluated for vascular sprouting. A more extensive endothelial sprouting was noted in Hpse- KO derived rings (right panel) as compared to wt derived rings (left panel). B. Matrigel plug assay. Hpse- KO (lower panels) and wt (upper panels) mice were injected subcutaneously with 200 µl of growth factor depleted Matrigel supplemented with FGF-2 (80 ng/ml). Seven days later, the Matrigel plugs were excised and photographed, followed by homogenization and determination of hemoglobin content using Drabkin's reagent (right). A pronounced angiogenic response was noted in Hpse- KO vs. wt mice (55±7.18 mg/dl vs. 21±6.2 mg/dl; p≤0.0002, respectively).

Article Snippet: Briefly, 1 mm mouse aortic rings were embedded in 3-dimensional growth factor depleted Matrigel (BD Biosciences, San Jose, CA), and incubated in 0.5 ml Bio-MPM (Biological industries, Beit haemek, Israel) in the absence or presence of added FGF-2 (50 ng/mL).

Techniques: Derivative Assay, Staining, Matrigel Assay, Injection, Homogenization

a Self-assembling peptide RADA16 molecular model. The calculated peptide dimensions are ~6 nm long depending on end capping, 1.3 nm wide and 0.8 nm thick. b Model of thousands of individual peptides as a single nanofiber. c Trilion of individual peptides self-assemble into nanofiber scaffold as revealed by the SEM. Scale bar = 0.5 µm. d RADA16-I peptide nanofibers scaffold hydrogel with extremely high-water content (99.5–99.0%, w/v water). An image of nanofiber scaffolds hydrogel of RADA16-I at 1% (10 mg/ml), 99% water (image courtesy of 3-D Matrix). e Murine neural stem cells are embedded in the nanofiber scaffold. The diameter of nanofiber is in the similar diameter as the cell produced extracellular matrix . f Red blood cells are embedded in the natural fibrin. g Dense RADA16 nanofiber scaffold . Billions of layers of interwoven nanofibers tightly keep blood cells in place thus preventing from bleeding.

Journal: NPJ Regenerative Medicine

Article Title: Self-assembling peptide scaffolds in the clinic

doi: 10.1038/s41536-020-00116-w

Figure Lengend Snippet: a Self-assembling peptide RADA16 molecular model. The calculated peptide dimensions are ~6 nm long depending on end capping, 1.3 nm wide and 0.8 nm thick. b Model of thousands of individual peptides as a single nanofiber. c Trilion of individual peptides self-assemble into nanofiber scaffold as revealed by the SEM. Scale bar = 0.5 µm. d RADA16-I peptide nanofibers scaffold hydrogel with extremely high-water content (99.5–99.0%, w/v water). An image of nanofiber scaffolds hydrogel of RADA16-I at 1% (10 mg/ml), 99% water (image courtesy of 3-D Matrix). e Murine neural stem cells are embedded in the nanofiber scaffold. The diameter of nanofiber is in the similar diameter as the cell produced extracellular matrix . f Red blood cells are embedded in the natural fibrin. g Dense RADA16 nanofiber scaffold . Billions of layers of interwoven nanofibers tightly keep blood cells in place thus preventing from bleeding.

Article Snippet: PuraMatrix ® is sold directly by 3-D Matrix and through distributors including Corning, VWR, Fisher Scientific, and others.

Techniques: Produced