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Rt-PCR help,come in


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#1 salmon

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Posted 09 August 2002 - 12:05 AM

I am a fresh one in trying RT. I use b-actin as control to compare different GENE. I think both primers should be put into the same tube. But At the first time we use 25 cycles,we could find b-actin stripe. After we change some characters, we could not find it at last. Could you give me a better protocol, or even a little advise on playing with RT-PCR? Thanks a lot.

#2 helene

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Posted 09 August 2002 - 03:08 AM

Hi!

I don't what protocol you use for RT-PCR.I recommand the use of the superscript II reverse transcriptase from life technologies and following the supplied protocol. If the lengh of your PCR Product is important remove the ARN with RNAse H after the reverse transcription . For the PCR try some differents annhiling temperature (55,60,65C for example. The time for elongation must be approximatively one minut per Kb (3 minuts for a PCR products of 3Kb). The Mg2+ concentration is also important try different: concentrations from 1 to 2mM for exemple. Put only 2l(maximum) of your RT product into the PCR

good luck

helene


#3 liuzhibingzp

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Posted 11 August 2002 - 02:27 AM

                       RT PCR PROTOCOL 1
               USING SUPERSCRIPT REVERSE TRANSCRIPTASE          
1First Strand cDNA Synthesis:Add the following components to a nuclease-free microcentrifuge tube,total reaction volume is 20ul:
     random primers:1ul 50-250 ng
     Total      RNA: 1-5 ug
     DEPC-treated water to 12 ul
Heat mixture to 70 for 10 min and quick chill on ice.
Collect the contents of the tube by brief centrifugation and add:
            Components        adding volume  Final concentration
     5X First Strand Buffer :       4ul            1mM
            0.1 M DTT               2ul           10mM
            10 mM dNTP              1ul           0.5mM
2 Mix contents of the tube gently and incubate at 42 for 2 min.
3Add 1 ul (200 units) of SUPERSCRIPT II, mix by pipetting gently up and down.
4. Incubation at 25 for 10 min
5. Incubate 50 min at 42.
6. Inactivate the reaction by heating at 70 for 15 min.

NOTE: The cDNA can now be used as a template for amplification in PCR. However, amplification of some PCR targets (those >1 kb) may require the removal of RNA complementary to the cDNA. To remove RNA complementary to the cDNA, add 1 ul (2 units) of E. coli RNase H and incubate 37 for 20 min.

II. PCR Reaction
   Use only 10% of the first strand reaction for PCR. Adding larger amounts of the first strand reaction may not increase amplification and may result in decreased amounts of PCR product.
1. Add the following to a PCR reaction tube for a final reaction volume of 100 ul:
          Components        adding volume   Final cincentration
        10X PCR Buffer          10ul              1mM
         50 mM MgCl2             3ul              1.5mM
         10 mM dNTP              2ul              0.2mM
      Primer 1 (10 uM)           2ul              0.2mM
      Primer 2 (10 uM)           2ul              0.2mM
Taq DNA polymerase (2-5 U/ul)    1ul
2 ul cDNA (from first strand reaction, preferably RNase H-treated)
Autoclaved, distilled water      80ul
2. Mix gently .
3. Perform 15 to 40 cycles of PCR.





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