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Zebrafish is convenient for transient genetic manipulations such as morpholino-mediated gene knockdown, DNA/mRNA-based genetic overexpression. These genetic approaches do not involve the challenge of making transgenic animals, and their effect can last up to a week. This protocol describes the detailed steps of injecting to zebrafish embryos.

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[Bio101] Injecting Zebrafish Embryos

Molecular Biology > DNA > Transformation
Author: Lili Jing
Lili JingAffiliation: Department of Cell and Molecular Biology, University of Pennsylvania, Philadelphia, USA
For correspondence: lilijingcn@gmail.com
Bio-protocol author page: a38
1/20/2011, 8647 views, 1 Q&A, How to cite
DOI: http://dx.doi.org/10.21769/BioProtoc.22

[Abstract] Zebrafish is convenient for transient genetic manipulations such as morpholino-mediated gene knockdown, DNA/mRNA-based genetic overexpression. These genetic approaches do not involve the challenge of making transgenic animals, and their effect can last up to a week. This protocol describes the detailed steps of injecting to zebrafish embryos.

Materials and Reagents

  1. Glass capillary tubing (Fisher)
  2. Zebrafish mating boxes (Aquatics)
  3. Mineral oil (Sigma)

Equipment

  1. Micropipette puller (Sutter instrument)
  2. Microinjection system Pico-injector (Harvard apparatus)
  3. Microscope (Leica)
  4. Micrometer slide (American 3B Scientific)
  5. Benchtop microcentrifuge (Biotool)

Procedure

  1. The night before:
    Set up 10-15 pairs of fish, keeping the male and female separated from one another. By doing this, the fish won’t mate until you are ready for them, but they will still be amenable to mating!
    Pull the needle using the needle puller according to the manufacture’s instructions.
  2. The morning of injections:
    1. Putting fish together (in the fish room)
      1. In each of 3-5 single boxes, combine the male and female fish so that the female will begin to lay eggs (egg laying will begin in 15-45 min, and the same fish may lay eggs more than one time).
    2. Filling Needles (in the injection room)
      1. Hang needle above bench
      2. Spin RNA/cDNA/dye sample in benchtop microfuge (30 sec) so that any debris will go to bottom of the tube
      3. Using gel loading tip, remove 1-1.5 μl of sample from tube and load into back end of needle
      4. Wait for capillary action to carry sample to needle tip
  3. Meanwhile…
    1. Collect eggs from the fish you have put together, labeling the dish with the date and type of fish and take them to the injection room
    2. Add embryos to injection dish and use forceps to push them into the individual rows
    3. Using forceps, rotate embryos so that the yolk is facing the future direction of the needle
    4. Remove enough E3 so that the embryos do not float, but be careful not to let them dry out!
    5. Set this dish aside while you break the needle.
  4. Breaking Needles
    1. Turn on air supply.
    2. Turn on injection apparatus and microscope light source.
    3. Set the Pinj to 25-30 kPa (turn "inject" knob to change)- the higher the P, the better for breaking the needle
    4. Make sure the Pout and Pbal are slightly positive (0.1-0.2) (turn "balance" knob, if needed)
    5. Place a drop of oil on micrometer slide, set this aside
    6. Insert filled needle into micromanipulator
    7. Find the end of the needle under the microscope (this will likely require you to move the needle with the micromanipulator until it comes into the field of view)
    8. Adjust the microscope to the highest magnification, keeping the end of the needle in view
    9. Using forceps, clip end of needle (This takes practice to clip the needle in the correct place!)
    10. Put micrometer slide in field of view
    11. Put tip of needle in oil on slide so that it is positioned over markings. Do not let the tip of the needle touch the slide!
    12. Adjust the injection time to 6-8 msec
    13. Step on the injection pedal->INJECT into oil and look at droplet size
    14. Adjust Pinj and injection time and continue to inject into the oil until the droplet is 0.12-0.15 mm (see chart on wall to calculate drop volume).
    15. The drop size can be larger, but it is more likely to be toxic to the embryo
    16. You are now ready to inject embryos!

      **Do not leave the broken needle tip exposed to the air for too long, or the RNA/cDNA/dye may dry and clog the tip of the needle. You may put the tip of the needle into a dish with water/E3 to keep it wet, but be sure to check that the water is not going into the needle, or that your sample is not leaking into the water!

      If the tip of the needle does clog, put the needle tip in some water/E3 and push the "clear" button. This will sometimes remove the clog.


How to cite this protocol: Jing, L. (2011). Injecting Zebrafish Embryos. Bio-protocol Bio101: e22. DOI: 10.21769/BioProtoc.22; Full Text



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10/17/2012 11:37:14 PM  

景 枫
协和医学院

请问E3是什么试剂?可以保证胚胎不悬浮不脱水。

10/25/2012 1:34:58 PM  

Lili Jing (Author)
Department of Cell and Molecular Biology,University of Pennsylvania

E3 是斑马鱼胚胎培养液。可以让其不脱水和保持活性。做显微注射的时候不要加太多E3,胚胎就不会悬浮。
配方见下。
60X E3 stock
(makes 2 liters)

34.4 g NaCl
1.52 g KCl
5.8 g CaCl2.2H2O
9.8 g MgSO4.7H2O
add double distilled water up to 2000 ml

Store in refrigerator. To dilute to 1X for rearing zebrafish, use 160 ml of stock and fill to 10 liters with ddH2O.

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