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Team:Cambridge/Protocols/Extraction of cleaner genomic DNA from squid
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==Extraction of cleaner genomic DNA from squid== | ==Extraction of cleaner genomic DNA from squid== | ||
| - | protocol | + | As the quick and dirty method to extract genomic DNA failed to produce genomic DNA suitable for PCR, two new protocols are carried out as an attempt to obtain cleaner genomic DNA. This protocol produces clearner preparations and probably somewhat higher yields of genomic DNA. |
===Theory=== | ===Theory=== | ||
How it works | How it works | ||
| - | ===Practice | + | ===Practice== |
| - | + | ||
{Standard layout for procedures is to use: | {Standard layout for procedures is to use: | ||
Revision as of 12:28, 1 August 2011
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Extraction of cleaner genomic DNA from squid
As the quick and dirty method to extract genomic DNA failed to produce genomic DNA suitable for PCR, two new protocols are carried out as an attempt to obtain cleaner genomic DNA. This protocol produces clearner preparations and probably somewhat higher yields of genomic DNA.
Theory
How it works
=Practice
{Standard layout for procedures is to use:
- <Procedure title - aka what you are doing>
- <step 1>
- <step 2>
- <additional notes/important information regarding the previous step>
the text within the < > is what should be written, don't include < > in actual writeup :P
if in doubt see the gel electrophoresis protocol
}
Safety
The safety implication of the procedure.
