Literature DB >> 19274045

Microinjection of zebrafish embryos to analyze gene function.

Jonathan N Rosen1, Michael F Sweeney, John D Mably.   

Abstract

One of the advantages of studying zebrafish is the ease and speed of manipulating protein levels in the embryo. Morpholinos, which are synthetic oligonucleotides with antisense complementarity to target RNAs, can be added to the embryo to reduce the expression of a particular gene product. Conversely, processed mRNA can be added to the embryo to increase levels of a gene product. The vehicle for adding either mRNA or morpholino to an embryo is microinjection. Microinjection is efficient and rapid, allowing for the injection of hundreds of embryos per hour. This video shows all the steps involved in microinjection. Briefly, eggs are collected immediately after being laid and lined up against a microscope slide in a Petri dish. Next, a fine-tipped needle loaded with injection material is connected to a microinjector and an air source, and the microinjector controls are adjusted to produce a desirable injection volume. Finally, the needle is plunged into the embryo's yolk and the morpholino or mRNA is expelled.

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Year:  2009        PMID: 19274045      PMCID: PMC2762901          DOI: 10.3791/1115

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  1 in total

1.  heart of glass regulates the concentric growth of the heart in zebrafish.

Authors:  John D Mably; Manzoor Ali P K Mohideen; C Geoffrey Burns; Jau-Nian Chen; Mark C Fishman
Journal:  Curr Biol       Date:  2003-12-16       Impact factor: 10.834

  1 in total
  75 in total

1.  Electro-microinjection of fish eggs with an immobile capillary electrode.

Authors:  Ryo Shirakashi; Tatsuo Yasui; Simon Memmel; Vladimir L Sukhorukov
Journal:  Biomicrofluidics       Date:  2015-11-25       Impact factor: 2.800

2.  Non-invasive Imaging of the Innate Immune Response in a Zebrafish Larval Model of Streptococcus iniae Infection.

Authors:  Elizabeth A Harvie; Anna Huttenlocher
Journal:  J Vis Exp       Date:  2015-04-21       Impact factor: 1.355

3.  Triggering Cell Stress and Death Using Conventional UV Laser Confocal Microscopy.

Authors:  Marco Morsch; Rowan A W Radford; Emily K Don; Albert Lee; Elinor Hortle; Nicholas J Cole; Roger S Chung
Journal:  J Vis Exp       Date:  2017-02-03       Impact factor: 1.355

4.  Non-invasive imaging of disseminated candidiasis in zebrafish larvae.

Authors:  Kimberly M Brothers; Robert T Wheeler
Journal:  J Vis Exp       Date:  2012-07-30       Impact factor: 1.355

5.  Measuring protein stability in living zebrafish embryos using fluorescence decay after photoconversion (FDAP).

Authors:  Katherine W Rogers; Alexander Blässle; Alexander F Schier; Patrick Müller
Journal:  J Vis Exp       Date:  2015-01-28       Impact factor: 1.355

6.  Analysis of gene function and visualization of cilia-generated fluid flow in Kupffer's vesicle.

Authors:  Guangliang Wang; H Joseph Yost; Jeffrey D Amack
Journal:  J Vis Exp       Date:  2013-03-31       Impact factor: 1.355

7.  Isolation of the Side Population in Myc-induced T-cell Acute Lymphoblastic Leukemia in Zebrafish.

Authors:  Margaret M Pruitt; Wilfredo Marin; Michael R Waarts; Jill L O de Jong
Journal:  J Vis Exp       Date:  2017-05-04       Impact factor: 1.355

8.  Invasive Behavior of Human Breast Cancer Cells in Embryonic Zebrafish.

Authors:  Jiang Ren; Sijia Liu; Chao Cui; Peter Ten Dijke
Journal:  J Vis Exp       Date:  2017-04-25       Impact factor: 1.355

9.  Forebrain electrophysiological recording in larval zebrafish.

Authors:  Scott C Baraban
Journal:  J Vis Exp       Date:  2013-01-24       Impact factor: 1.355

10.  Modeling mucosal candidiasis in larval zebrafish by swimbladder injection.

Authors:  Remi L Gratacap; Audrey C Bergeron; Robert T Wheeler
Journal:  J Vis Exp       Date:  2014-11-27       Impact factor: 1.355

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