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Articles by Kenric J. Hoegler in JoVE

 JoVE Neuroscience

लक्ष्य निर्धारण घ्राण बल्ब संयुक्त का प्रयोग न्यूरॉन्स Vivo में Electroporation और Gal4 आधार बढ़ाने जाल Zebrafish लाइन्स


JoVE 2964 8/15/2011

1Department of Biology, Pace University, 2Cellular and Molecular Medicine, University of California, San Diego, 3Division of Cell Biology and Cell Physiology, Zoological Institute, Braunschweig University of Technology

आनुवंशिक जोड़तोड़ के अस्थायी और स्थानिक संकल्प जैविक घटना है कि वे उपद्रव कर सकते हैं की स्पेक्ट्रम निर्धारित करता है. यहाँ हम अस्थायी और spatially असतत उपयोग

Other articles by Kenric J. Hoegler on PubMed

Targeting the Zebrafish Optic Tectum Using in Vivo Electroporation

INTRODUCTION: In vivo electroporation is a method for delivery of plasmids and other oligonucleotide reagents that offers precise temporal control. In zebrafish, in vivo electroporation is particularly well-suited to delivering green fluorescent protein (GFP) expression vectors to the developing central nervous system. This protocol describes a modification of in vivo electroporation that can be used to specifically target the developing optic tectum of zebrafish embryos beginning at 24 h post-fertilization (hpf). The electroporation electrodes required for this approach can be constructed easily from relatively inexpensive materials. Microinjection of plasmid DNA to the midbrain ventricle followed by precise positioning of the electroporation electrodes allows for the targeting of developing neurons in only one hemisphere of the optic tectum. Using this protocol, the optic tectum can be effectively targeted in a high percentage (79%) of expressing embryos. This method can also be used to simultaneously deliver expression vectors and loss-of-function reagents, which can provide precise temporal control of the knockdown of gene function.

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