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General PCR instrument operating procedures1. Boot operation2. (1) Turn on the power switch of the PCR machine. (2) Push the top cover of the PCR machine back, and then put the PCR thin-walled tube in it. (3) Push the top cover of the PCR machine forward, and press down the back buckle evenly.
READ MOREWhy are the bands amplified on different models of PCR instruments different in brightness?Answer: Different PCR machines have different optimized heating and cooling strategies. Therefore, when transferring the PCR step parameters used on this type of CR machine to another type of PCR machine, it i
READ MOREGene amplification laboratory, also known as PCR laboratory, is characterized by the ability to greatly increase trace amounts of DNA and is widely used in various fields of biology.In principle, the PCR laboratory is divided into four separate working areas: reagent preparation area
READ MORE
Real-time Q-PCR has a wide range of applications, including the study of mRNA expression, the detection of DNA copy number, and the determination of single nucleotide polymorphisms (SNPs). The following is an overview of the current applications of real-time Q-PCR in translocation gene detection
General PCR instrument operating procedures1. Boot operation2. (1) Turn on the power switch of the PCR machine. (2) Push the top cover of the PCR machine back, and then put the PCR thin-walled tube in it. (3) Push the top cover of the PCR machine forward, and press down the back buckle evenly.
Why are the bands amplified on different models of PCR instruments different in brightness?Answer: Different PCR machines have different optimized heating and cooling strategies. Therefore, when transferring the PCR step parameters used on this type of CR machine to another type of PCR machine, it i
Gene amplification laboratory, also known as PCR laboratory, is characterized by the ability to greatly increase trace amounts of DNA and is widely used in various fields of biology.In principle, the PCR laboratory is divided into four separate working areas: reagent preparation area
Real-time Q-PCR has a wide range of applications, including the study of mRNA expression, the detection of DNA copy number, and the determination of single nucleotide polymorphisms (SNPs). The following is an overview of the current applications of real-time Q-PCR in translocation gene detection
General PCR instrument operating procedures1. Boot operation2. (1) Turn on the power switch of the PCR machine. (2) Push the top cover of the PCR machine back, and then put the PCR thin-walled tube in it. (3) Push the top cover of the PCR machine forward, and press down the back buckle evenly.
Gene amplification laboratory, also known as PCR laboratory, is characterized by the ability to greatly increase trace amounts of DNA and is widely used in various fields of biology.In principle, the PCR laboratory is divided into four separate working areas: reagent preparation area
Principle of PCR thermal cyclerThe essence of PCR technology is in vitro nucleic acid amplification, heating to unscrew double-stranded DNA, hybridization of primers with template DNA under annealing temperature conditions, extension of primers in the presence of Taq DNA polymerase, dNTPs
