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Vector Laboratories
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Vector Laboratories
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Italia Srl
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Merck KGaA
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BioLynx Inc
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KEYENCE
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Vector Laboratories
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Image Search Results
Journal: Frontiers in neurology
Article Title: Inside the Thrombus: Association of Hemostatic Parameters With Outcomes in Large Vessel Stroke Patients.
doi: 10.3389/fneur.2021.599498
Figure Lengend Snippet: FIGURE 3 | Matrix metalloproteinase-10 (MMP-10) and thrombin-activatable fibrinolysis inhibitor (TAFI) colocalize with inflammatory cells and platelets in thrombi. Double immunofluorescence for MMP-10 (top, red) and TAFI (bottom, red) and leukocytes (CD45, left), macrophages CD68 (middle), and platelets CD42b (right, green); cell nuclei are stained with 4′,6-diamidino-2-phenylindole (DAPI) (blue). Arrow heads point to double positive cells for MMP-10 (upper panels) and TAFI (lower panels) and the specified antigens (yellow). Scale = 20 µm.
Article Snippet: Finally, slides were mounted with
Techniques: Staining
Journal: Frontiers in neurology
Article Title: Inside the Thrombus: Association of Hemostatic Parameters With Outcomes in Large Vessel Stroke Patients.
doi: 10.3389/fneur.2021.599498
Figure Lengend Snippet: FIGURE 4 | Matrix metalloproteinase-10 (MMP-10) and thrombin-activatable fibrinolysis inhibitor (TAFI) colocalization in thrombi. Immunofluorescence for TAFI (red), MMP-10 (green), and 4′,6-diamidino-2-phenylindole (DAPI) (blue). Arrow heads point to double positive cells for MMP-10 and TAFI. Scale = 20 and 10 µm.
Article Snippet: Finally, slides were mounted with
Techniques:
Journal: STAR Protocols
Article Title: Combining electrophysiology and optogenetics for functional screening of pyramidal neurons in the mouse prefrontal cortex
doi: 10.1016/j.xpro.2021.100469
Figure Lengend Snippet: Experimental setup and essential equipment for in utero electroporation (A) Image of the whole setup for in utero electroporation. (B) Images of the electroporator to deliver electrical stimulation to pups (upper) and the micro injector to inject the plasmids (lower). (C) Images of surgical implements and a glass pipette which contains the diluted solution including plasmids for in utero electroporation. (D) Scheme of the in utero electroporation. The plasmid is injected into the fetal lateral ventricle and electrical stimulation is delivered via the forceps-shaped bipolar electrode. The electroporation is performed on 6–8 embryos in a single operation. (E) Inject the solution containing the plasmid into one side of the lateral ventricles on each embryo. The injection site of the plasmid should be 0.75–1.0 mm anterior from lambda and 0.5 mm lateral from the sagittal suture. (F) The positions of the electrode to target the mPFC. Note that the negative pole is positioned over the injected hemisphere while the positive one is positioned on the contralateral side. The two electrodes are slightly angled rostrocaudally and vertically as seen. (G–I) Low (G) and high (H) magnification Images of injection of the plasmids and image of delivering electrical stimulation through a forceps-shape electrode (I) during in utero electroporation. (J) Image of the mPFC from an electroporated mouse. The green signal shows GFP and the blue signal represents DAPI staining. Scale, 1mm. (K) High-magnification image of the electroporated mPFC expressing GFP. Scale, 50 μm. See also .
Article Snippet:
Techniques: In Utero, Electroporation, Transferring, Plasmid Preparation, Injection, Staining, Expressing
Journal: STAR Protocols
Article Title: Combining electrophysiology and optogenetics for functional screening of pyramidal neurons in the mouse prefrontal cortex
doi: 10.1016/j.xpro.2021.100469
Figure Lengend Snippet:
Article Snippet:
Techniques: Recombinant, Mutagenesis, Transfection, Blocking Assay, Expressing, Plasmid Preparation, DNA Purification, cDNA Synthesis, Ligation, Software, In Utero, Electroporation, Microscopy