Biotechnology Training Courses at the National Institutes of Health
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BIO-TRAC

FAES/NIH
Building 60
Room 237
1 Cloister Court
Bethesda, MD
20814-1460

301-496-8290

 

Courses Offered:

Recombinant DNA Methodology
siRNA: Principles and Applications
Realtime and Quantitative PCR

Recombinant DNA Methodology
January 2 - January 7, 2007

Conventional PCR has revolutionized the detection and analysis of nucleic acids. However, one of its major limitations has been the inability to accurately quantitate the amount of product, which reflects the amount of starting material, due to differing plateau effects among multiple samples. The need to accurately determine quantitative changes in gene expression has led to the adoption of real-time RT-PCR as the method of choice not only for quantitative gene expression but also for validating results obtained from array analyses and other techniques that evaluate gene expression changes on a global scale.

This lecture/laboratory course is intended for those who have a fundamental background in PCR and will address the basic chemistries of real time PCR and the many platforms available.

Register Now

siRNA: Principles and Applications
May 29 - June 2, 2007

Studies of post-transcriptional gene silencing (PTGS) led to the discovery of the phenomenon of RNA interference (RNAi) and the role-played in that process by small interfering RNA (siRNA). Although only recently identified, siRNA molecules already are taking the research world by storm as their potential as functional genomic tools is beginning to be appreciated. Compared to antisense and knockout techniques, siRNA can more rapidly and effectively create loss-of-function phenotypes and they may even provide an approach for gene therapy.

In this hands-on lecture-lab workshop participants will learn the latest information about RNAi and the use of siRNA as a functional genomics tool.

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Realtime and Quantitative PCR
September 4 - September 9, 2007

Conventional PCR has revolutionized the detection and analysis of nucleic acids. However, one of its major limitations has been the inability to accurately quantitate the amount of product, which reflects the amount of starting material, due to differing plateau effects among multiple samples. The need to accurately determine quantitative changes in gene expression has led to the adoption of real-time RT-PCR as the method of choice not only for quantitative gene expression but also for validating results obtained from array analyses and other techniques that evaluate gene expression changes on a global scale.

This lecture/laboratory course is intended for those who have a fundamental background in PCR and will address the basic chemistries of real time PCR and the many platforms available.

Register Now

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Biotechnology Training Courses at the National Institutes of Health
Sponsored by the Foundation for Advanced Education in the Sciences