Esophageal Adenocarcinoma Methods and Protocols

(sharon) #1
225

4 Notes



  1. PCR hood should be exposed to ultraviolet light for 25 min
    prior to using it.

  2. Master reaction mixture is all the required ingredients to run
    a PCR reaction excluding the template. For example, for 2×
    PCR mastermix protocol, prepare 10 μL 2× mastermix, 1 μL
    of 10 μM gene forward primer, and 1 μL of 10 μM gene
    reverse primer.

  3. Prepare an extra reaction for every eight reactions in consider-
    ation of pipetting error and evaporation.

  4. For every sample, three technical replicates are
    recommended.

  5. Three biological samples in duplicates (six reactions in total)
    with one non-template control and one extra reactions.

  6. It is recommended to use between 50 and 500 ng of template
    when working with genomic DNA.

  7. Non-template control is prepared by replacing the template
    with DNase-free water.

  8. Set the lid temperature to 105 °C or closest temperature avail-
    able on the PCR machine used.

  9. For every 100 mL of 1× TAE buffer, dissolve 2 g of agarose
    powder. Ensure that agarose powder is completely dissolved
    by heating in bursts of a few seconds and agitating flask at each
    cycle. Once the gel is fully dissolved, quickly but carefully
    transfer the solution onto the agarose gel cast. Ensure that all
    bubbles are removed from the gel and leave to solidify.

  10. Using conical flask helps prevent overflowing of agarose liquid
    when heating it in the microwave oven.

  11. Routinely check the electrophoresis run to ensure that the
    band does not run over the gel.

  12. Protocol may vary from manufacturer to manufacturer.

  13. Usage of DNase-free water rather than the provided elution
    buffer can help improve Sanger sequencing result. In addition,
    total volume of DNase-free water used during elution can be
    reduced if a higher concentration of elute is desired.

  14. Optimal primer annealing temperature for Sanger sequencing
    protocol should be around 60–65 °C.

  15. Prepare an extra 10% of additional volume to compensate for
    pipetting error and evaporation.

  16. If bubbles are present at the top of the well, or in small quanti-
    ties, it will not adversely affect the reaction.


Single Gene Mutation in Esophageal Adenocarcinoma
Free download pdf