![Learn DNA Primer Design for Polymerase Chain Reaction]()
MP4 | Video: h264, 1280x720 | Audio: AAC, 44100 Hz
Language: English | Size: 294 MB | Duration: 33m
In this Bioinformatics
course you will be find out how to DNA Pr Design for polymerase chain reaction.
What you'll learn
Learn how to design DNA Pr for any PCR Test like SARS-nCoV2, AIDS Detection
Understand Mapping and Sequencing of genomes, Cloning, Basic Research
Understand Basic feature Polymerase Chain Reaction and their Steps
Learn two Bioinformatics tools used for manual method pr designing Cluster W Oligucalculator
Learn one Bioinformatics tools used for manual method pr designing Pr 3
Understand specific Parameters of Pr Design
Used Forensics Science filed for DNA Amplification
Requirements
Basic Knowledge Computer
Basic Science Knowledge
Description
Pr BLAST performs only a specificity check when a target template and both prs are provided. Design prs for single- or multi-insert cloning or for your site-directed mutagenesis expent (insertion, deletion, replacement) with our pr design tool. Pr3 is a computer program that suggests PCR prs for a variety of applications, for example to create STSs (sequence tagged sites) for radiation hybrid mapping, or to amplify sequences for single nucleotide polymor- phism discovery
Polymerase chain reaction (PCR) steps
Denaturing
Annealing
Extension
Specification of Pr Design
Aim for the GC content to be between 40 and 60% with the 3' of a pr ending in G or C to promote binding
A good length for PCR prs is generally around 18-30 bases.
Try to make the melting temperature (Tm) of the prs between 65°C and 75°C, and within 5°C of each other
A good length for PCR prs is generally around 18-30 bases. Specificity usually is dependent on length and annealing temperature. The shorter the prs are, the more efficiently they will bind or anneal to the target.
However, a pr should not be too long 30-mer prs) or too short. Short prs produce inaccurate, nonspecific DNA amplification product, and long prs result in a slower hybridizing rate. ... One also needs to avoid pr-pr annealing which creates pr dimers and disrupts the amplification process
Who this course is for:
Undergraduate Student
Master Student
Entry Level Pr Designer
Biotechnology and Bioinformatics
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