1994
DOI: 10.1159/000133628
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Localization of the human cholecystokinin-B/gastrin receptor gene (CCKBR) to chromosome 11p15.5→p15.4 by fluorescence in situ hybridization

Abstract: A human cholecystokinin-B/gastrin receptor cDNA (CCKBR) has been recently cloned and its transcriptional product has been characterized. The cDNA probe was mapped by fluorescence in situ hybridization to chromosome 11 at bands p15.5→p15.4. The localization of this receptor gene provides a useful marker for this region of chromosome 11 permitting the identification of diseases involving the gene and interactions with other genes.

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Cited by 30 publications
(18 citation statements)
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“…A 4.1-kb FRP genomic fragment obtained from a human fibroblast genomic DNA library (Stratagene) was labeled with biotin or digoxigenin and used as a probe for in situ hybridization to locate the FRP gene in chromosomal preparations of methotrexate-synchronized normal peripheral human lymphocyte cultures. The conditions for hybridization, detection of fluorescent signal, digital-image acquisition, processing, and analysis were as described (26). The identity of the chromosomes with specific signal was confirmed by rehybridization using a chromosome 8-specific probe, and the signal was localized on G-banded chromosomes.…”
Section: Methodsmentioning
confidence: 99%
“…A 4.1-kb FRP genomic fragment obtained from a human fibroblast genomic DNA library (Stratagene) was labeled with biotin or digoxigenin and used as a probe for in situ hybridization to locate the FRP gene in chromosomal preparations of methotrexate-synchronized normal peripheral human lymphocyte cultures. The conditions for hybridization, detection of fluorescent signal, digital-image acquisition, processing, and analysis were as described (26). The identity of the chromosomes with specific signal was confirmed by rehybridization using a chromosome 8-specific probe, and the signal was localized on G-banded chromosomes.…”
Section: Methodsmentioning
confidence: 99%
“…Chromosomes were obtained from peripheral lymphocyte cultures after methotrexate-thymidine release treatments and used for fluorescence in situ hybridization (FISH) as described previously (29,54). The probes were labeled by nick translation with biotin-dUTP or digoxigen-11-dUTP.…”
Section: Methodsmentioning
confidence: 99%
“…Lambda clone lMAM1 and subclone pMAM4.3 were labeled with biotin or digoxigenin using a random-prime DNA labeling kit (Boehringer-Mannheim). FISH was performed as perviously described (Zimonjic et al, 1994). Slides were pretreated with RNase, denatured in 26SSC/ 70% formamide for 2 min at 708C, and hybridized with 200 ng of DNA probe in 26SSC/50% formamide/10% dextran sulfate/26Denhart's/1% Tween20 for 18 h at 378C.…”
Section: Chromosomal Mappingmentioning
confidence: 99%