Development and application of a real-time quantitative PCR assay for determining CYP1A transcripts in three genera of salmonids

Aquatic Toxicology

Volumn 66, Issue 4, 2004, Pages 357-368

  Rees, Christopher B ^a   Li, Weiming ^a  

^a MICHIGAN STATE UNIVERSITY   (United States)

Author keywords

cDNA sequence; CYP1A; P450; Real time quantitative PCR; Salmon; Trout

Indexed keywords

BETA NAPHTHOFLAVONE; COMPLEMENTARY DNA; CORN OIL; CYTOCHROME P450 1A; FISH PROTEIN; HEMOPROTEIN; LIVER ENZYME; MESSENGER RNA; RNA;

BIOASSAY; ECOTOXICOLOGY; GENE EXPRESSION; POLLUTION EXPOSURE; POLYMERASE CHAIN REACTION; SALMONID;

3' UNTRANSLATED REGION; AMINO ACID SEQUENCE; ANIMAL TISSUE; ARTICLE; ATLANTIC SALMON; BASE PAIRING; CONTROLLED STUDY; DNA SEQUENCE; FISH GENETICS; FLUORESCENCE; GENE EXPRESSION; GENE INDUCTION; GENETIC ANALYSIS; LIVER; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYADENYLATION; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; RAINBOW TROUT; REAL TIME POLYMERASE CHAIN REACTION; SALMONID; START CODON; STOP CODON;

FONTINALIS; ONCORHYNCHUS; ONCORHYNCHUS MYKISS; PISCES; SALMO; SALMO SALAR; SALMONIDAE; SALVELINUS; SALVELINUS FONTINALIS; SALVELINUS NAMAYCUSH; TELEOSTEI; ZEA MAYS;

EID: 1042266253     PISSN: 0166445X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.aquatox.2003.10.004     Document Type: Article

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