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
1. Scanning for single nucleotide polymorphisms (SNPs), HRMA primer design, and primer validation SNP identification in wild-type laboratory colony mosquitoes 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, …
Representative Results
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 and primer design. Abbreviations: SNP = single nucleotide polymorphism; sgRNA = single guide RNA; LVP = Liverpool strain.
Divulgaciones
The authors have nothing to disclose.
Materials
70% Ethanol
70% ethanol solution in water
96-well PCR and Real-time PCR plates
VWR
82006-636
For obtaining genomic DNA (from the mosquito leg)
96-well plate templates
House-made printed, for genotype recording
Bio Rad CFX96
Bio Rad
PCR machine with gradient and HRMA capabilities
Diversified Biotech reagent reservoirs
VWR
490006-896
Exo-CIP Rapid PCR Cleanup Kit
New England Biolabs
E1050S
Glass Petri Dish
VWR
89001-246
150 mm x 20 mm
Nunc Polyolefin Acrylate Sealing tape, Thermo Scientific
VWR
37000-548
To use with the 96-well PCR plates for obtaining genomic DNA
Phire Animal tissue direct PCR Kit (without sampling tools)
Thermo Fisher
F140WH
For obtaining genomic DNA and performing PCR
Precision Melt Analysis Software
Bio Rad
1845025
Used for genotyping the mosquito DNA samples and analyzing the thermal denaturation properties of double-stranded DNA (see protocol step 3.3)
Single-channel pipettor
Gilson
Phire Animal tissue direct PCR Kit (without sampling tools)