In vitro DNA amplification (PCR)

II. Development and applications in the veterinary area

Authors

  • D. Hirigoyen División Citogenética, Instituto de Investigaciones Biológicas "Clemente Estable" (IIBCE). Montevideo.
  • H. Bruzzoni Giovanelli División Citogenética, Instituto de Investigaciones Biológicas "Clemente Estable" (IIBCE). Montevideo.
  • C. Azambuja División Citogenética, Instituto de Investigaciones Biológicas "Clemente Estable" (IIBCE). Montevideo.
  • M. Stoll División Citogenética, Instituto de Investigaciones Biológicas "Clemente Estable" (IIBCE). Montevideo. Unidad de Biotecnología. Estación Experimental "Las Brujas". Instituto Nacional de Investigaciones Agropecuarias, INIA.

Keywords:

Veterinary diagnostic, Molecular biology, Genetic markers, Gene, PCR

Abstract

The principal improvement in the detection systems had carried a rapid change in the diagnostic technology. The direct, indirect, radioactive and non radioactive systems usually used are more sensitive than traditional methods. Since the brief existence of Molecular Biology as a science several contributions had lead to the vertiginous technology revolution to what we now assist. They include: "restriction enzimes" that cut the DNA in specific sequences; nucleics and proteins sequencing, Restriction Fragments Large Polimorphism (RFLPs) and recently the PCR. In the first part the instrumentation and basic fundaments of PCR were described, and now in this paper the authors purpose is to relate a few technic applications in the veterinarian area.

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Published

1992-09-01

How to Cite

Hirigoyen, D. ., Bruzzoni Giovanelli, H., Azambuja, C., & Stoll, M. (1992). In vitro DNA amplification (PCR): II. Development and applications in the veterinary area. Veterinaria (Montevideo), 28(117), 14–22. Retrieved from https://revistasmvu.com.uy/index.php/smvu/article/view/758

Issue

Section

Review Articles