AlanFung:Protocol/Capturing: Difference between revisions
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==Reagent Preparation== | |||
dNTP concentration 10mM(NEB) | |||
ddH2O Ligase Buffer Ligase Amplitaq dNTP | |||
2U/ul AmpliTaq Stoffel fragment; 0.5U/ul AmpLigase; 1mM dNTP: 0.5ul 0.1ul 0.1ul 0.2ul (10mM)0.1ul | |||
x30 15ul 3ul 3ul 6ul 3ul | |||
==Overview== | ==Overview== | ||
*Bisulfite Conversion of DNA | *Bisulfite Conversion of DNA | ||
*Capturing Reaction | *Capturing Reaction | ||
==Calculation== | ===Calculation=== | ||
Probe:target ratio 200:1 | Probe:target ratio 200:1 (according to Alice, 100:1 works too) | ||
*Billy uses 250ng | |||
NIH_3T3_gDNA Template(100ng/uL) | NIH_3T3_gDNA Template(100ng/uL) | ||
Use 200ng total, so = 2uL | Use 200ng total, so = 2uL | ||
*One genome mass = 3pg | *One genome mass = 3pg | ||
Line 23: | Line 29: | ||
==Procedures== | ==Procedures== | ||
==Bilsulfite Conversion with EZ DNA Methylation-Gold Kit== | |||
*Add 900ul ddH2O, 300ul M-Dilution Buffer and 50ul M-Dissolving Buffer to a tube of CT Conversion Reagent vortex for 10M | |||
*Add 24mL of 100% ethanol to the 6mL M-Wash Buffer concentrate | |||
of CT Conversion Reagent | *Add 130ul of CT conversion reagent to samples. If your DNA sample is less than 20uL make up the difference with H2O | ||
*Mix the sample and perform | |||
*98C 10min -> 64C 150min -> 4c overnight. | |||
*Add 600ul M-Binding buffer to spin columns. | |||
*Add the converted samples to the columns, close the gap and mix by inverting several times. | |||
*Spin at 15,000rpm for 30sec, discard flow through | |||
*Add 100ul M-Wash Buffer, spin for 30 sec, discard flow-through. | |||
*Add 200ul M-Desulphonation Buffer, wait for 20min, spin at 15,000 rpm for 30sec. | |||
*Add 200ul M-Wash Buffer, spin for 30 sec. | |||
*Place the columns into 1.5ml tubes, add 10ul M-Elution Buffer. Wait for 1min, spin at 15,000rpm for 30sec. | |||
*Measure the DNA with Nanodrop: | |||
RNA | |||
* | |||
Add | |||
Add | |||
Add | |||
Add | |||
Add | |||
Place | |||
Measure | |||
==Capturing System Setup== | ==Capturing System Setup== | ||
CT Converted Ms-gDNA | CT Converted Ms-gDNA | ||
10X AmpLigase buffer | 10X AmpLigase buffer | ||
Ms_Meth Probe (242.4nM) | Ms_Meth Probe (242.4nM) | ||
H2O | H2O | ||
Total | Total | ||
95c 10min -> 60C 24h ->add 2ul SLN mix(2U/ul AmpliTaq Stoffel fragment; 0.5U/ul AmpLigase; 1mM dNTP) -> 60C 4h -> <BR>4 cycels (95C 1min -> 55C for 4h),add 2ul more SLN mix after 1st cycle -> 95C 5min -> <BR>add 2ul Exonuclease I/III mixadd 2ul Exonuclease I/III mix as soon as the temperature is lowered to 37C -> 37C 1h -> 94C 5min -> 4C hold | |||
Latest revision as of 00:43, 18 October 2009
Reagent Preparation[edit]
dNTP concentration 10mM(NEB) ddH2O Ligase Buffer Ligase Amplitaq dNTP 2U/ul AmpliTaq Stoffel fragment; 0.5U/ul AmpLigase; 1mM dNTP: 0.5ul 0.1ul 0.1ul 0.2ul (10mM)0.1ul x30 15ul 3ul 3ul 6ul 3ul
Overview[edit]
- Bisulfite Conversion of DNA
- Capturing Reaction
Calculation[edit]
Probe:target ratio 200:1 (according to Alice, 100:1 works too) *Billy uses 250ng NIH_3T3_gDNA Template(100ng/uL) Use 200ng total, so = 2uL
- One genome mass = 3pg
- First calculate the # of genome your target represents
- For 200ng, it represents 200ng/3pg=66666.67 genomes
- You want to have 200x the probes as the target 200ng/3pg*200
- You want every single probe to target ratio to be 200:1 200ng/3pg*200*55,000
Ms_Meth 22ng/uL 55,000Probes 100nt Since 1 base = 330Da (for single stranded DNA, 660Da for ds), the concentration of probe is 22 ng/ul /(100x330) = 0.000666667 = 666.67nM # of molecules per mole = 6X10^23 # of probes needed/ concentration of probes = Volume of probes needed the volume the probe needed is 200ng/3pg x 200 x 55,000 / [(6x10^23)x (666.67*10^-9M)]*10^6 =1.83uL
Procedures[edit]
Bilsulfite Conversion with EZ DNA Methylation-Gold Kit[edit]
- Add 900ul ddH2O, 300ul M-Dilution Buffer and 50ul M-Dissolving Buffer to a tube of CT Conversion Reagent vortex for 10M
- Add 24mL of 100% ethanol to the 6mL M-Wash Buffer concentrate
- Add 130ul of CT conversion reagent to samples. If your DNA sample is less than 20uL make up the difference with H2O
- Mix the sample and perform
- 98C 10min -> 64C 150min -> 4c overnight.
- Add 600ul M-Binding buffer to spin columns.
- Add the converted samples to the columns, close the gap and mix by inverting several times.
- Spin at 15,000rpm for 30sec, discard flow through
- Add 100ul M-Wash Buffer, spin for 30 sec, discard flow-through.
- Add 200ul M-Desulphonation Buffer, wait for 20min, spin at 15,000 rpm for 30sec.
- Add 200ul M-Wash Buffer, spin for 30 sec.
- Place the columns into 1.5ml tubes, add 10ul M-Elution Buffer. Wait for 1min, spin at 15,000rpm for 30sec.
- Measure the DNA with Nanodrop:
RNA
Capturing System Setup[edit]
CT Converted Ms-gDNA 10X AmpLigase buffer Ms_Meth Probe (242.4nM) H2O Total 95c 10min -> 60C 24h ->add 2ul SLN mix(2U/ul AmpliTaq Stoffel fragment; 0.5U/ul AmpLigase; 1mM dNTP) -> 60C 4h ->
4 cycels (95C 1min -> 55C for 4h),add 2ul more SLN mix after 1st cycle -> 95C 5min ->
add 2ul Exonuclease I/III mixadd 2ul Exonuclease I/III mix as soon as the temperature is lowered to 37C -> 37C 1h -> 94C 5min -> 4C hold