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Vectashield R Hardset Tm Antifade Mountng Medium, supplied by Vector Laboratories, 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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Vector Laboratories vectashield media with dapi
Vectashield Media With Dapi, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Merck KGaA vectashield® hardset tm antifade mounting medium with dapi
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 <t>DAPI</t> staining. Scale, 1mm. (K) High-magnification image of the electroporated mPFC expressing GFP. Scale, 50 μm. See also .
Vectashield® Hardset Tm Antifade Mounting Medium With Dapi, supplied by Merck KGaA, 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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BioLynx Inc vectashield antifade mounting medium containing dapi vecth20002
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 <t>DAPI</t> staining. Scale, 1mm. (K) High-magnification image of the electroporated mPFC expressing GFP. Scale, 50 μm. See also .
Vectashield Antifade Mounting Medium Containing Dapi Vecth20002, supplied by BioLynx 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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KEYENCE vectashield antifade mounting medium containing dapi
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 <t>DAPI</t> staining. Scale, 1mm. (K) High-magnification image of the electroporated mPFC expressing GFP. Scale, 50 μm. See also .
Vectashield Antifade Mounting Medium Containing Dapi, supplied by KEYENCE, 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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96
Vector Laboratories vectashield vibrance antifade mounting medium
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 <t>DAPI</t> staining. Scale, 1mm. (K) High-magnification image of the electroporated mPFC expressing GFP. Scale, 50 μm. See also .
Vectashield Vibrance Antifade Mounting Medium, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/vectashield vibrance antifade mounting medium/product/Vector Laboratories
Average 96 stars, based on 1 article reviews
vectashield vibrance antifade mounting medium - by Bioz Stars, 2026-02
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Vector Laboratories vectashield antifade mounting medium
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 <t>DAPI</t> staining. Scale, 1mm. (K) High-magnification image of the electroporated mPFC expressing GFP. Scale, 50 μm. See also .
Vectashield Antifade Mounting Medium, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/vectashield antifade mounting medium/product/Vector Laboratories
Average 97 stars, based on 1 article reviews
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Image Search Results


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 .

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: VECTASHIELD® HardSet TM Antifade Mounting Medium with DAPI , Merck Millipore , CAT: # H-1500-10.

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: VECTASHIELD® HardSet TM Antifade Mounting Medium with DAPI , Merck Millipore , CAT: # H-1500-10.

Techniques: Recombinant, Mutagenesis, Transfection, Blocking Assay, Expressing, Plasmid Preparation, DNA Purification, cDNA Synthesis, Ligation, Software, In Utero, Electroporation, Microscopy