Method Article

Wild-Type Blocking PCR to Detect Low-Frequency Somatic Mutations

July 8th, 2025

In This Article

Abstract

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Source: Albitar, A. Z. et al., Wild-type Blocking PCR Combined with Direct Sequencing as a Highly Sensitive Method for Detection of Low-Frequency Somatic Mutations. J. Vis. Exp. (2017).

This video describes wild-type blocking polymerase chain reaction, or WTB-PCR, which detects somatic mutations. The PCR-based technique uses a locked nucleic acid, or LNA, an oligonucleotide that binds to its complementary wild-type allele and blocks its elongation. The blocking selectively allows the amplification of low-level mutant alleles over their wild-type variants in the sample.

Protocol

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1. DNA Extraction from FFPE Tissue, Peripheral Blood, and Bone Marrow Aspirate

  1. For bone marrow FFPE tissue with DNA FFPE extraction kit
    1. Begin with FFPE tissue from unstained slides (5 - 10 sections at 5 - 10 µm thickness).
      NOTE: If beginning with tissue shavings, use 3 - 6 sections at 5 - 10 µm thickness and skip to step 1.1.6.
    2. Place slides in a slide basket and prepare four wash reservoirs (two for Xylene and two for 100% Alcohol). Add a minimum volume of 600 mL of the solution to each basket.
    3. Deparaffinize the slides by doing a 5 min xylene wash in the first tray. Transfer the slides to....

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Disclosures

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No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
1.5 or 2 mL Safe-Lock microcentrifuge tubesEppendorf05-402-25
100% alcoholVWR89370-084Histology grade; 91.5% Ethanol, 5% Isopropyl alcohol, 4.5% Methyl alcohol
Aluminium sealing foilsGeneMateT-2451-1For PCR and cold storage
Centrifuge 5804 SeriesEppendorfA-2-DWP rotor (for PCR plate)
Cold plate for 96-well platesEppendorfZ606634
DNAse, RNAse-free, ultra-pure water
dNTPs (100 mM)Invitrogen10297-117
Ethanol AbsoluteSigmaE7023200 proof, for molecular biology
Exiqon website Oligo Toolshttp://www.exiqon.com/oligo-tools
FastStart Taq DNA polymerase (5 U/µL)Roche12032937001With10x concentrated PCR reaction buffer, with 20 mM MgCl2
Gel electrophoresis apparatus2% agarose gel
LNA oligonucleotideExiqon5001005'-TCAGA+AG+C+G+A+C+T+G+A +T+CC/invdT/ (+N = LNA bases)
Mastercycler Pro S ThermocyclerEppendorfE950030020
Microcentrifuge Model 5430EppendorfFA-45-30-11 rotor (for 1.5/2 mL microcentrifuge tubes)
NanoDrop 2000 SpectrophotometerThermo Fisher Scientific
PCR forward primerIDT5'-tgt aaa acg acg gcc agt TGC CAG GGG TAC TTA GAT GG
PCR reverse primerIDT5'-cag gaa aca gct atg acc GGT TGG TGT AGT CGC AGA CA
PCR platesGeneMateT-3107-1
Pipettors20, 200, 1,000 µL
QIAamp DNA Mini KitQiagen51304For BM aspirate and peripheral blood
Vortex genieScientific IndustriesSI-0236
Slide basket

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Tags

Wild type Blocking PCRSomatic Mutation DetectionLocked Nucleic AcidLNA OligonucleotideDNA Polymerase BlockingMutant Allele AmplificationPrimer DesignMelting Temperature PredictionOligo OptimizationThermocycling Protocol

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