2000Unpublished venueRequires access

PRINSIP UMUM DAN PELAKSANAAN POLYMERASE CHAIN REACTION (PCR)[General Principles and Implementation of Polymerase Chain Reaction]

Darmo Handoyo, Ari Rudiretna

Open publisher page 21 citations

Abstract

Polymerase Chain Reaction (PCR) is an in vitro technique for the amplification of a specific DNA region without prior transfer into living cells. It is a powerful technique because a million-fold amplification can be achieved only in a few hours. For the carrying out of PCR, pair of primers are needed that flank the DNA region to be amplified. A primer is an oligonucleotide with a nucleotide sequence complementary to the nucleotide sequence in the DNA template. This paper will discuss the general principles of PCR, the detailed procedure for carrying out the PCR and the various factors affecting the optimal PCR results. This technique was introduced by Kary Mullis in 1985, for which he obtained the Nobel Prize in 1993.

About this research paper

What this paper is about

Polymerase Chain Reaction (PCR) is an in vitro technique for the amplification of a specific DNA region without prior transfer into living cells. It is a powerful technique because a million-fold amplification can be achieved only in a few hours. For the carrying out of PCR, pair of primers are needed that flank the DNA region to be amplified. A primer is an oligonucleotide with a nucleotide sequence complementary to the nucleotide sequence in the DNA template. This paper will discuss the general principles of PCR, the detailed procedure for carrying out the PCR and the various factors affecting the optimal PCR results. This technique was introduced by Kary Mullis in 1985, for which he obtained the Nobel Prize in 1993.

Why it matters

OpenAlex reports 21 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Polymerase Chain Reaction (PCR) is an in vitro technique for the amplification of a specific DNA region without prior transfer into living cells. It is a powerful technique because a million-fold amplification can be achieved only in a few hours. For the carrying out of PCR, pair of primers are needed that flank the DNA region to be amplified. A primer is an oligonucleotide with a nucleotide sequence complementary to the nucleotide sequence in the DNA template. This paper will discuss the general principles of PCR, the detailed procedure for carrying out the PCR and the various factors affecting the optimal PCR results. This technique was introduced by Kary Mullis in 1985, for which he obtained the Nobel Prize in 1993.

Key concepts: Hot start PCR, Polymerase chain reaction optimization, Polymerase chain reaction, Inverse polymerase chain reaction, Primer (cosmetics), Molecular biology, Applications of PCR, Oligonucleotide

Related papers

Back to paper searchBrowse research topicsOriginal source
PRINSIP UMUM DAN PELAKSANAAN POLYMERASE CHAIN REACTION (PCR)[General Principles and Implementation of Polymerase Chain Reaction] — Research Paper | ScholarLens