1998
DOI: 10.1016/s0168-1702(98)00022-7
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Development and application of polymerase chain reaction (PCR) tests for the detection of subgroup J avian leukosis virus

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Cited by 159 publications
(128 citation statements)
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“…The negative control used was DNA from uninoculated CEF. The primer sequences were prepared as follows: a 0.7-kb fragment corresponding to the 3' end of the pol and 5' part of the env regions was obtained by PCR using a primer set, H5 (5'-GGA TGA GGT GAC TAA GAA AG-3') and H2 (5'-ACT GGT GAA TCC ACA ATA TCT ACG-3') [20] from the brain tissue of a bantam affected with fowl glioma and cloned into pGEM-T vector (Promega Corp., Madison, WI, U.S.A.). The resultant fragment was sequenced using an ABI PRISM 310 Genetic Analyzer (Perkin-Elmer Applied Biosystems Inc., Foster City, CA, U.S.A.).…”
Section: Chicken and Inoculummentioning
confidence: 99%
“…The negative control used was DNA from uninoculated CEF. The primer sequences were prepared as follows: a 0.7-kb fragment corresponding to the 3' end of the pol and 5' part of the env regions was obtained by PCR using a primer set, H5 (5'-GGA TGA GGT GAC TAA GAA AG-3') and H2 (5'-ACT GGT GAA TCC ACA ATA TCT ACG-3') [20] from the brain tissue of a bantam affected with fowl glioma and cloned into pGEM-T vector (Promega Corp., Madison, WI, U.S.A.). The resultant fragment was sequenced using an ABI PRISM 310 Genetic Analyzer (Perkin-Elmer Applied Biosystems Inc., Foster City, CA, U.S.A.).…”
Section: Chicken and Inoculummentioning
confidence: 99%
“…Analysis of PCR assays with ALV-J specific primers (Smith et al, 1998) revealed positive reaction with DNA obtained from tumors, indicating that the viral particles which were observed in transmission electron microscopy were ALV-J.…”
Section: Discussionmentioning
confidence: 98%
“…The sequences of the oligonucleotide primers (H5 and H7) used in the study were selected from the published sequences (Smith et al, 1998). Primers were obtained from Life Technologies 2 .…”
Section: Methodsmentioning
confidence: 99%
“…The extraction of RNA from frozen livers was performed using TRIzol Reagent (Gibco-BRL Life Technologies, U.S.A.) according to the manufacturer's instructions. RT-PCR based on specific primers H5 (5'-GGA TGA GGT GAC TAA GAA AG-3') and H7 (5'-CGA ACC AAA GGT AAC ACA CG-3') [8] of subgroup J ALV was performed using a commercial kit (Ready-To-Go RT-PCR Beads, Amersham Pharmacia Biotech, U.S.A.). A mixture (50 µl) containing 46 or 47 µl of diethylpyrocarbonate-treated water (Bio 101, Inc., U.S.A.), 1 µl of each primer and 1 or 2 µl of template RNA was added to the reagents for reverse transcription in the kit.…”
Section: Reverse Transcriptase-polymerase Chain Reaction (Rt-pcr)mentioning
confidence: 99%