Hypochlorite Dechorionation

Hypochlorite dechorionation is a laboratory method that removes the protective chorion surrounding embryos, making embryonic development easier to observe and manipulate in developmental biology. The process uses a dilute hypochlorite solution to chemically degrade the chorion, followed by thorough rinsing to stop exposure and protect the embryo. In zebrafish research, dechorionated embryos support clearer imaging, direct access for microinjection or experimental treatments, and more consistent assessment of morphology and developmental events. Because exposure time and solution strength affect embryo viability, careful handling is essential for obtaining reliable results in studies of embryogenesis, environmental effects, and developmental mechanisms.

Hypochlorite Dechorionation - Related Videos

Research

JoVE EoE - Drosophila melanogaster (fruit fly)

Drosophila Egg Collection and Dechorionation: A Method to Remove the Outermost Egg Layer

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2023

The Drosophila embryo is surrounded by protective outer membranes. To gain access to the embryo, the chorion–the outermost of the membranes–is often removed. This video describes a commonly used method of dechorionation using sodium hypochlorite. The example protocol demonstrates the procedure while employing sterile techniques necessary for axenic or gnotobiotic animal rearing.

Research

JoVE Journal - Biology
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Dechorionation of Medaka Embryos and Cell Transplantation for the Generation of Chimeras

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Cited by 20 •

2010

Due to the hard chorion and soft embryos, manipulation of medaka embryos is more involved than in zebrafish. This video shows step-by-step procedures for how to manipulate medaka embryos, including dechorionation, mounting in agarose for imaging and cell transplantation for the production of chimeras. These procedures are essential to use medaka and zebrafish in a laboratory to take full advantage of their complementary features for the genetic dissection of vertebrate genome functions.

Embryo Microinjection and Electroporation in the Chordate Ciona intestinalis

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Cited by 17 •

2016

We present transient transgenesis and gene knockdown in Ciona intestinalis, a chordate sister group to vertebrates, using microinjection and electroporation techniques. Such methods facilitate functional genomics in this simple invertebrate that features rudimentary characteristics of vertebrates, including notochord and head sensory epithelia, and many orthologs of human disease associated genes.

Using a Sandwich ELISA to Determine the Immunogenic Glycoprotein Content in a Vaccine

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2025

This video showcases an indirect enzyme-linked immunosorbent assay or ELISA sandwich immunocapture assay designed to assess immunogenic glycoprotein levels in vaccines. The assay plate, containing glycoprotein-specific antibodies, is incubated with serially diluted vaccine samples, including reference and test vaccines, followed by immunoassay to quantify glycoprotein content in the test vaccine.

Rearing the Fruit Fly Drosophila melanogaster Under Axenic and Gnotobiotic Conditions

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Cited by 128 •

2016

A method for rearing Drosophila melanogaster under axenic and gnotobiotic conditions is presented. Fly embryos are dechorionated in sodium hypochlorite, transferred aseptically to sterile diet, and reared in closed containers. Inoculating diet and embryos with bacteria leads to gnotobiotic associations, and bacterial presence is confirmed by plating whole-body Drosophila homogenates.

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