GeneReach Biotechnology Corporation

PCR Training Program

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A. Safety operation in a PCR lab: Hazardous chemicals.. Safety rules for machines operation.. Reagent preservation and lab security.

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B. Basic theory of PCR

  • DNA structure.
  • The function of DNA Polymerase.
  • The principle of polymerase chain reaction (PCR).
  • Basic requirements and design of PCR lab.
  • Potential problems of PCR.

C. Introduction of PCR related reagents:

  • Nucleic acid extraction kit.
  • IQ2000/IQREAL/IQ Plus /POCKIT Reagent Set.

D. Introduction of PCR related equipment E. Review of some major diseasesF. Basic theory of viral disease prevention

  • Avoid vertical transmission.
  • Avoid horizontal transmission.
A. Practice of DNA extractionB. Practice of PCR operation procedure
  • Reaction condition.
  • Reagents preparation.
  • Reaction Procedure.
C. Practice of gel electrophoresis if needed:
  • Agarose gel preparation.
  • Electrophoresis.
  • Gel staining and data assay.
D. Sampling procedure and sample preservation
  • Preservation of samples.
  • Preservation of nucleic acid samples.
  • Introduction of sample dissecting tools.
  • Disinfection procedure of the sample dissecting tools.
  • Sampling strategy.

A. Perform the assay by using real samples

  • To compare the sensitivity, reproducibility, and to practice more, it is necessary to go through the whole procedure by real samples again.
  • Positive standards and negative control are required.
  • Requirements of sample.

B. Detail description of PCR diagnostic procedure

  • Sampling, sensitivity, and statistical issue.
  • False positive or false negative result.
  • Reproducibility.
  • Lab management.

C. How to integrate the diagnostic results into real practice.

A. Real samples operation: to confirm the operation and process the other diagnostic systems.B. Discussion.