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June 2, 2008 at 10:50 am #18956
Seung Jae JeongParticipantNorthern Hybridization for tRNA
Sep. 24. 2001.
Joong-Won Lee
*Sample preparation
-Total RNA preparation
a.RNA prep. by Trizol method(1)
b.The pellet is dissolved in appropreate volume of 10mM NaOAc(pH4.5) 1mM EDTA or 250mM Tris-Cl(pH9.6). store at -70C0
c.Control sample:deacylation:250mM Tris-Cl(pH9.6) incubation at 37C0 for 30min
*Gel preparation
-10% polyacrylamide(19:1), 8M Urea, 100mM NaOAc(pH5.0), 1X TBE.(2,3)
a.12.5ml 40% polyacrylamide(19:1) / 24g Urea/ 1.66ml 3M NaOAc(pH5.0)/ 5ml 10XTBE
b.Adjust the volume to 50ml with H2O.
c.add 400ul 10% APS and 30ul TEMED
*Electrophoresis
-Running Buffer:1X TBE.
Sample buffer:0.1M NaOAc(pH5.0)/ 8M Urea/ 0.05% XC,BPB(4)
a.Sample buffer:RNA sample=1.5:1
b.running for 5hr at 500V.
*Transfer
-Electronic transfer/transfer buffer:40mM Tris-acetate pH8.1
a.Semi-dry transblotter 3hr (width X length = mA)
*Labeling of antisense oligonucleotides
-Probe Labeling:gamma32P end labeling:incubation at 37C0 for 30min
a.phosphorylation reaction
oligonucleotide 100ng(2ul)/
gamma-32P ATP(3ul)/
nuclease-free water(3ul)/
T4 polynucleotide kinase(10unit/ul)1ul/
Incubation at 37C0 for 30min
stop the reaction by adding 1ul of 0.5M EDTA
b.removal of unincoporated label
sephadex G-25 column
*UV crosslinking and Hybridization
-UV crosslinking the transferred nylon membrane
-Hybridization sol:30% formamide/ 5Xdenhardt′s sol/ 5X SSC/ 0.1% SDS
a.prehybridization:add 100ul ssDNA(10mg/ml stock) to 10ml hybridization sol and incubation at 37C0 for 2hr
b.hybridization:add probe and incubation at 37C0 for 17hr
c.washing and expose:
2X SSC(0.1% SDS)/ 1X SSC(0.1% SDS)/ 0.1X SSC(0.1% SDS)
Reference
1. Anal.Biochem. 1987. 161:156-158
2. P.N.A.S. 1987. 84:2185-1051
3. J.B.C. 1991. 266:24712-24718
4. M.C.B. 1996 16:907-913
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