Method Article

Gradient Polymerase Chain Reaction to Determine the Optimum Annealing Temperature

July 8th, 2025

In This Article

Abstract

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Source: Tsujimoto, H. et al., Indel Detection following CRISPR/Cas9 Mutagenesis using High-resolution Melt Analysis in the Mosquito Aedes aegypti. J. Vis. Exp. (2021).

This video demonstrates the gradient polymerase chain reaction for optimization of the annealing temperature of primers, which sets gradient annealing temperature along wells. The effect of different annealing temperatures is determined by the yield of amplified products that helps to optimize the reaction condition.

Protocol

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1. Scanning for single nucleotide polymorphisms (SNPs), HRMA primer design, and primer validation

  1. SNP identification in wild-type laboratory colony mosquitoes
    1. Select the target exon to disrupt proper polypeptide translation.
      NOTE: The target should be close to the start codon or amongst key residues required for protein function. The shorter the exon (e.g., ≤200 bases), the more difficult it is to target and analyze. Avoid editing close to the boundaries of an exon, as this forces one of the HRMA primers to either cross an intron or be in an intron. This is undesirable because SNP rates tend to be much greater in ....

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Results

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SNP-rich DNA sequence diagram highlighting sgRNA-primer design regions for genetic research.
Figure 1: SNP identification. Schematic representation of multiple sequence alignment of AaeZIP11 fragment from wild-type. In red are the SNPs, and in green are the fragments free of SNPs; this SNP-free region is suggested for sgRNA an.......

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Disclosures

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No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
70% Ethanol70% ethanol solution in water
96-well PCR and Real-time PCR platesVWR82006-636For obtaining genomic DNA (from the mosquito leg)
96-well plate templatesHouse-made printed, for genotype recording
Bio Rad CFX96Bio RadPCR machine with gradient and HRMA capabilities
Diversified Biotech reagent reservoirsVWR490006-896
Exo-CIP Rapid PCR Cleanup KitNew England BiolabsE1050S
Glass Petri DishVWR89001-246150 mm x 20 mm
Nunc Polyolefin Acrylate Sealing tape, Thermo ScientificVWR37000-548To use with the 96-well  PCR plates for obtaining genomic DNA
Phire Animal tissue direct PCR Kit (without sampling tools)Thermo FisherF140WHFor obtaining genomic DNA and performing PCR
Precision Melt Analysis SoftwareBio Rad1845025Used for genotyping the mosquito DNA samples and analyzing the thermal denaturation properties of double-stranded DNA (see protocol step 3.3)
Single-channel pipettorGilson
Phire Animal tissue direct PCR Kit (without sampling tools)Thermo FisherF140WHFor obtaining genomic DNA and performing PCR
SeqMan ProDNAstar Lasergene softwareFor multiple sequence alignment
Single-channel pipettorGilson

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Tags

Gradient Polymerase Chain ReactionAnnealing Temperature OptimizationPrimer Annealing TemperatureThermal Cycler GradientDNA Amplification AnalysisNon specific AmplificationSpecific DNA AmplificationPCR Master Mix PreparationThermal Melt ProfilesOptimum Annealing Temperature

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