[northern] Northern Hybridization for tRNA

This topic has 0 replies, 1 voice, and was last updated 15 years, 11 months ago by Seung Jae Jeong.

  • Author
    Posts
    • #18955

      Seung Jae Jeong
      Participant

      Northern 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

       

       

       

Viewing 0 reply threads

You must be logged in to reply to this topic.

CONTACT US

We're not around right now. But you can send us an email and we'll get back to you, asap.

Sending

©2010-2024 Medicinal Bioconvergence Research Center. All rights reserved.

Log in with your credentials

Forgot your details?