Rui:Haplotying: Difference between revisions
>RuiLiu |
>RuiLiu |
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0.2% TritonX-100 | 0.2% TritonX-100 | ||
(0.1 AU/ml Qiagen Proteinase 7.5AU) | (0.1 AU/ml Qiagen Proteinase 7.5AU) | ||
Step 2: Proteinase and aliquot | Step 2: Proteinase and aliquot | ||
Add Proteinase right before aliquot, 1ul per tube, to 20 tubes. Store at -80C. | Add Proteinase right before aliquot, 1ul per tube, to 20 tubes. Store at -80C. | ||
Step 3: gDNA Tagmentation | Step 3: gDNA Tagmentation | ||
Line 33: | Line 35: | ||
55C for 5min | 55C for 5min | ||
Quick spin and cool down on ice | Quick spin and cool down on ice | ||
Step 4: Addition of T7 adaptor by Kapa system (?) | Step 4: Addition of T7 adaptor by Kapa system (?) | ||
Tagmented gDNA 5ul | Tagmented gDNA 5ul | ||
Kapa master mix | Kapa master mix 1X | ||
(dNTP;polymerase) | (dNTP;polymerase) | ||
0.5uM T7 adaptor 1ul | 0.5uM T7 adaptor 1ul | ||
100* SYBR green 0.25ul | 100* SYBR green 0.25ul | ||
Nf water up to 50ul | Nf water up to 50ul | ||
'''Total | '''Total 50ul''' | ||
''' | |||
72C, 3min; 95C, 30sec | |||
95C, 10sec; 62C, 30sec; 72C, 3min; 5 cycles | |||
Step 5: ExoI (SAP) treatment (?) | |||
Removal of T7 adaptor is a must for IVT, maybe optional for PCR as the following step... | |||
10U/ul ExoI mixed with 1U/ul SAP as 1.5~5U:1U, add 2ul (?) for each tube | |||
37C, 30min; 80C, 15-25min | |||
Step 6: Mix and EtOH precipitation | |||
Mix 10 tubes (~500ul) for EtOH precipitation | |||
Glycoblue 2ul | |||
NaOAc 50ul | |||
EtOH 1250ul | |||
'''Total 1800ul''' | |||
==Primers== | ==Primers== |
Revision as of 23:46, 16 March 2011
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 1X (dNTP;polymerase) 0.5uM T7 adaptor 1ul 100* SYBR green 0.25ul Nf water up to 50ul Total 50ul
72C, 3min; 95C, 30sec
95C, 10sec; 62C, 30sec; 72C, 3min; 5 cycles
Step 5: ExoI (SAP) treatment (?)
Removal of T7 adaptor is a must for IVT, maybe optional for PCR as the following step...
10U/ul ExoI mixed with 1U/ul SAP as 1.5~5U:1U, add 2ul (?) for each tube
37C, 30min; 80C, 15-25min
Step 6: Mix and EtOH precipitation
Mix 10 tubes (~500ul) for EtOH precipitation
Glycoblue 2ul NaOAc 50ul EtOH 1250ul Total 1800ul
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>