Oligonucleotide primers for polymerase chain reaction amplification of human immunoglobulin variable genes and design of family‐specific oligonucleotide probes
- 1 April 1991
- journal article
- research article
- Published by Wiley in European Journal of Immunology
- Vol. 21 (4), 985-991
- https://doi.org/10.1002/eji.1830210419
Abstract
In recent work, the polymerase chain reaction (PCR) has been used to amplify rearranged mouse and human immunoglobulin heavy and χ light chain variable (V) genes. Here we have optimized the design of the PCR primers for human V genes and used them to amplify cDNA from human peripheral blood lymphocytes. Cloning and sequencing revealed a diverse repertoire of V genes, and the presence of members of each human V gene family. After alignment of the sequences, we identified a region conserved within V gene families, but differing between families, and used this to design family-specific oligonucleotide probes.Keywords
This publication has 39 references indexed in Scilit:
- The Croonian Lecture, 1989 Antibodies: a paradigm for the biology of molecular recognitionProceedings of the Royal Society of London. B. Biological Sciences, 1990
- Binding activities of a repertoire of single immunoglobulin variable domains secreted from Escherichia coliNature, 1989
- Rapid cloning of rearranged immunoglobulin genes from human hybridoma cells using mixed primers and the polymerase chain reactionBiochemical and Biophysical Research Communications, 1989
- Polymerase Chain Reaction with Single-Sided Specificity: Analysis of T Cell Receptor δ ChainScience, 1989
- The human VK locusJournal of Molecular Biology, 1988
- Two Unusual Human Immunoglobulin VκGenesBiological Chemistry Hoppe-Seyler, 1988
- A novel family of variable region genes of the human immunoglobulin heavy chainJournal of Molecular Biology, 1987
- Organization and evolution of variable region genes of the human immunoglobulin heavy chainJournal of Molecular Biology, 1986
- A large section of the gene locus encoding human immunoglobulin variable regions of the Kappa type is duplicatedJournal of Molecular Biology, 1985
- A Method for Isolation of Intact, Translationally Active Ribonucleic AcidDNA, 1983