Chromosome localization of two human serine protease genes to region 14q11.2----q12 by in situ hybridization. 1990

C C Lin, and M Meier, and O Sorensen, and R Sasi, and T Tainaka, and R C Bleackley
Department of Pathology, University of Alberta, Edmonton, Canada.

Two human serine protease genes have been cloned. One corresponds to CTLA1, the human equivalent of the mouse cytotoxic cell protease gene Ctla-1, and the other is novel. Both genes were localized to 14q11.2----q12 by in situ hybridization. This result confirms the assignment of human CTLA1 to 14q11.2----q12 and provides new mapping data for another human serine protease gene located in the same chromosome region.

UI MeSH Term Description Entries
D009693 Nucleic Acid Hybridization Widely used technique which exploits the ability of complementary sequences in single-stranded DNAs or RNAs to pair with each other to form a double helix. Hybridization can take place between two complimentary DNA sequences, between a single-stranded DNA and a complementary RNA, or between two RNA sequences. The technique is used to detect and isolate specific sequences, measure homology, or define other characteristics of one or both strands. (Kendrew, Encyclopedia of Molecular Biology, 1994, p503) Genomic Hybridization,Acid Hybridization, Nucleic,Acid Hybridizations, Nucleic,Genomic Hybridizations,Hybridization, Genomic,Hybridization, Nucleic Acid,Hybridizations, Genomic,Hybridizations, Nucleic Acid,Nucleic Acid Hybridizations
D002874 Chromosome Mapping Any method used for determining the location of and relative distances between genes on a chromosome. Gene Mapping,Linkage Mapping,Genome Mapping,Chromosome Mappings,Gene Mappings,Genome Mappings,Linkage Mappings,Mapping, Chromosome,Mapping, Gene,Mapping, Genome,Mapping, Linkage,Mappings, Chromosome,Mappings, Gene,Mappings, Genome,Mappings, Linkage
D002883 Chromosomes, Human, Pair 14 A specific pair of GROUP D CHROMOSOMES of the human chromosome classification. Chromosome 14
D003001 Cloning, Molecular The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells. Molecular Cloning
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012697 Serine Endopeptidases Any member of the group of ENDOPEPTIDASES containing at the active site a serine residue involved in catalysis. Serine Endopeptidase,Endopeptidase, Serine,Endopeptidases, Serine
D015342 DNA Probes Species- or subspecies-specific DNA (including COMPLEMENTARY DNA; conserved genes, whole chromosomes, or whole genomes) used in hybridization studies in order to identify microorganisms, to measure DNA-DNA homologies, to group subspecies, etc. The DNA probe hybridizes with a specific mRNA, if present. Conventional techniques used for testing for the hybridization product include dot blot assays, Southern blot assays, and DNA:RNA hybrid-specific antibody tests. Conventional labels for the DNA probe include the radioisotope labels 32P and 125I and the chemical label biotin. The use of DNA probes provides a specific, sensitive, rapid, and inexpensive replacement for cell culture techniques for diagnosing infections. Chromosomal Probes,DNA Hybridization Probe,DNA Probe,Gene Probes, DNA,Conserved Gene Probes,DNA Hybridization Probes,Whole Chromosomal Probes,Whole Genomic DNA Probes,Chromosomal Probes, Whole,DNA Gene Probes,Gene Probes, Conserved,Hybridization Probe, DNA,Hybridization Probes, DNA,Probe, DNA,Probe, DNA Hybridization,Probes, Chromosomal,Probes, Conserved Gene,Probes, DNA,Probes, DNA Gene,Probes, DNA Hybridization,Probes, Whole Chromosomal

Related Publications

C C Lin, and M Meier, and O Sorensen, and R Sasi, and T Tainaka, and R C Bleackley
January 1989, Cytogenetics and cell genetics,
C C Lin, and M Meier, and O Sorensen, and R Sasi, and T Tainaka, and R C Bleackley
February 1991, Genomics,
C C Lin, and M Meier, and O Sorensen, and R Sasi, and T Tainaka, and R C Bleackley
April 1991, The Journal of biological chemistry,
C C Lin, and M Meier, and O Sorensen, and R Sasi, and T Tainaka, and R C Bleackley
January 1999, Cytogenetics and cell genetics,
C C Lin, and M Meier, and O Sorensen, and R Sasi, and T Tainaka, and R C Bleackley
January 1990, Cytogenetics and cell genetics,
C C Lin, and M Meier, and O Sorensen, and R Sasi, and T Tainaka, and R C Bleackley
May 1996, Somatic cell and molecular genetics,
C C Lin, and M Meier, and O Sorensen, and R Sasi, and T Tainaka, and R C Bleackley
January 1996, Cytogenetics and cell genetics,
C C Lin, and M Meier, and O Sorensen, and R Sasi, and T Tainaka, and R C Bleackley
August 1982, Proceedings of the National Academy of Sciences of the United States of America,
C C Lin, and M Meier, and O Sorensen, and R Sasi, and T Tainaka, and R C Bleackley
January 1997, Cytogenetics and cell genetics,
C C Lin, and M Meier, and O Sorensen, and R Sasi, and T Tainaka, and R C Bleackley
January 1990, Cytogenetics and cell genetics,
Copied contents to your clipboard!