Inhaltsangabe
PCR is the most powerful technique currently used in molecular biology. It enables the scientist to quickly replicate DNA and RNA on the benchtop. From its discovery in the early 80's, PCR has blossomed into a method that enables everything from ready mutation of DNA/RNA to speedy analysis of tens of thousands of nucleotide sequences daily.PCR Applications examines the latest developments in this field. It is the third book in the series, building on the previous publications PCR Protocols and PCR Strategies. The manual discusses techniques that focus on gene discovery, genomics, and DNA array technology, which are contributing factors to the now-occurring bioinformatics boom.
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The polymerase chain reaction is the most powerful technique currently used in molecular biology laboratories. From its discovery in the early 80s, PCR has blossomed into a method that enables everything from ready mutation of DNA to speedy analysis of tens of thousands of nucleotide sequences daily.
PCR Applications: Protocols for Functional Genomics examines the latest PCR implementations. It complements the other books in the series, PCR Protocols (1990) and PCR Strategies (1995), and techniques discussed are relevant to the now-occurring bioinformatics and proteomics boom.
Key Features:
* focuses on gene discovery, genomics, and DNA array technology
* covers quantitative PCR techniques, including the use of standards and kinetic analysis
* includes statistical refinement of primer design parameters
* illustrates techniques used in microscopic tissue samples, such as single cell PCR, whole cell PCR, laser capture microdissection, and in situ PCR|The polymerase chain reaction is the most powerful technique currently used in molecular biology laboratories. From its discovery in the early 80s, PCR has blossomed into a method that enables everything from ready mutation of DNA to speedy analysis of tens of thousands of nucleotide sequences daily.
PCR Applications: Protocols for Functional Genomics examines the latest PCR implementations. It complements the other books in the series,PCR Protocols (1990) and PCR Strategies (1995), and techniques discussed are relevant to the now-occurring bioinformatics and proteomics boom.
Key Features:
* focuses on gene discovery, genomics, and DNA array technology
* covers quantitative PCR techniques, including the use of standards and kinetic analysis
* includes statistical refinement of primer design parameters
* illustrates techniques used in microscopic tissue samples, such as single cell PCR, whole cell PCR, laser capture microdissection, andin situ PCR
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