Rui:Haplotying: Difference between revisions
Jump to navigation
Jump to search
>RuiLiu |
>Sam Chiang |
||
Line 2: | Line 2: | ||
==Protocol== | ==Protocol== | ||
[[File:Design.ppt]] | |||
*Cell lysis buffer (1*) | |||
20mM EDTA | |||
10mM Tris-HCl (pH 8) | |||
200mM NaCl | |||
0.2% TritonX-100 | |||
(0.1 AU/ml Qiagen Proteinase) | |||
==Primers== | ==Primers== |
Revision as of 20:05, 2 February 2011
Background
Protocol
- Cell lysis buffer (1*)
20mM EDTA 10mM Tris-HCl (pH 8) 200mM NaCl 0.2% TritonX-100 (0.1 AU/ml Qiagen Proteinase)
Primers
File:Primers for Tn-based-haplotyping.xls
2011
<calendar> name=Rui:LabNotes/SingleCell format=%name/%year-%month-%day date=2011/10/1 view=oneyear </calendar>