Rui:Haplotying: Difference between revisions

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==Background==


Original: [[File:Design.ppt]]
Modified: [[File:Tn-based-haplotyping V1.1.ppt]]
==Protocol==
Step 1: Cell lysis
Collect 10 cells in 20ul lysis buffer.
Cell lysis buffer (1*)
200mM NaCl
20mM EDTA
10mM Tris-HCl (pH 8)
0.2% TritonX-100
(0.1 AU/ml Qiagen Proteinase 7.5AU)
Step 2: Proteinase and aliquot
Add Proteinase right before aliquot, 1ul per tube, to 20 tubes. Store at -80C.
Step 3: gDNA Tagmentation
* 1:50 dilution of Nextera transposomes: 1ul Nextera enzyme in 24ul TE and 25ul 100% Glyceral
gDNA         1ul
5X HMW buffer 1ul
transposomes 1ul
Nf water 2ul
'''Total         5ul'''
55C for 5min
Quick spin and cool down on ice
Step 4: Addition of T7 adaptor by Kapa system (?)
Tagmented gDNA         5ul
Kapa master mix 10ul
(dNTP;polymerase)
0.5uM T7 adaptor 1ul
100* SYBR green 0.25ul
Nf water         up to 50ul
'''Total                 50ul
'''
==Primers==
[[File:Primers for Tn-based-haplotyping.xls]]
==2011==
<calendar>
name=Rui:LabNotes/Haplotyping
format=%name/%year-%month-%day
date=2011/10/1
view=oneyear
</calendar>

Latest revision as of 00:56, 7 December 2011