DNA Extraction Protocol
Extraction protocol
Remove a tiny piece of gill tissue with tweezers. Use isopropyl alcohol and then lighter in between to sterilize tweezers.
30 microliters 0.5 M NaOH.
Macerated with micropestle
Let stand for 10 minutes.
Add 150 microliters 100mM tris-HCL. Pipette mix.
10 minutes at 95 celsius heat bath.
Centrifuge 11,000 RPM, remove supernatant.
Freeze if needed (-20 degrees celcius) for future use.
- Published on Oct 06, 2024
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