How to manage PCR Products with Lab Management Software

PCR Consumables validation with Lab Management Software

PCR consumables are supplies that are used during the polymerase chain reaction (PCR) process. PCR consumables include items such as PCR Strip tubes, 96 Well Plates and tips. Other PCR consumables include  primers, enzymes, and reagents. They are used to amplify specific DNA or RNA sequences in a sample using the PCR process. The consumables are typically disposable and are used in one-time experiments or procedures. 

PCR consumables are used in a laboratory setting to amplify specific DNA or RNA sequences in a sample using the polymerase chain reaction (PCR) process. The specific steps involved in using PCR consumables may vary depending on the type of experiment being conducted and the specific consumables being used. However, some general steps that are involved include: 

  1. Setting up the PCR reaction: This typically involves preparing a mixture of the sample, primers, enzymes, and other reagents in a PCR tube or plate
  1. Amplifying the DNA or RNA: The mixture is then subjected to a series of temperature cycles using a thermal cycler during which the DNA or RNA is amplified through the action of the enzymes. 
  1. Analyzing the amplified product: Once the amplification is complete, the amplified DNA or RNA can be analyzed using a variety of techniques, such as gel electrophoresis or real-time PCR. 

Overall, the use of PCR consumables allows researchers to amplify specific DNA or RNA sequences rapidly and accurately in a sample, which can be used for a wide range of applications, including gene expression analysis, disease diagnosis, and genetic testing. 

How Using Qualer’s Initial and ongoing validation keeps you compliant

Maintaining system validation requires time and effort you can’t afford to waste. At Qualer, we offer our GAMP®5 Lab Management Software validation package that allows you to use the system in compliance with 21 CFR Part 11 from the minute you join. With our reliable management of the IQ/OQ/PQ documentation and processes needed for system validation, we minimize the compliance work so you don’t have to.

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