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PMID: 2655672 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Specificity of polymerase chain amplification reactions for human immunodeficiency virus type 1 DNA sequences.

AIDS research and human retroviruses ·Vol. 5 ·No. 1 ·1989-02-00 ·Pages 87-95

Bell J, Ratner L

Abstract

The polymerase chain amplification reaction (PCR) is a sensitive, specific, and quantitative assay of human immunodeficiency virus type 1 (HIV-1). The assay was performed with polymerases from Escherichia coli or Thermus aquaticus (Taq). A single pair of oligonucleotide primers within the long terminal repeat (LTR) sequences were used to detect HIV-1 sequences in infected cell cultures and fresh tissues of the large majority of infected individuals. The amplified product was a faithful copy of this LTR sequence. Utilization of a subsaturating number of cycles of amplification allowed quantitation of HIV-1 DNA sequences.

MeSH Terms
Base Sequence Cells, Cultured DNA Polymerase I DNA, Viral/analysis,genetics Escherichia coli/enzymology HIV-1/genetics Humans Molecular Sequence Data Nucleic Acid Amplification Techniques Oligodeoxyribonucleotides/genetics Terminator Regions, Genetic Thermus/enzymology
Chemicals
DNA, Viral Oligodeoxyribonucleotides DNA Polymerase I
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bell J
Division of Hematology and Oncology, Washington University, St. Louis, MO 63110.
Ratner L
Article Info
Journal
AIDS research and human retroviruses
Abbr.
AIDS Res Hum Retroviruses
ISSN
0889-2229
Published
1989-02-00
Pages
87-95
Language
English
Region
United States
NLM ID
8709376
Subset
IM
Grants
NIAID NIH HHS · AI25903-01-SRC · United States
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