Strategy of the use of 28S rRNA as a housekeeping gene in real-time quantitative PCR analysis of gene transcription in insect cells infected by viruses

Journal of Virological Methods

Volumn 163, Issue 2, 2010, Pages 210-215

  Xue, Jian Li ^a   Salem, Tamer Z ^a   Turney, Colin M ^a   Cheng, Xiao Wen ^a  

^a MIAMI UNIVERSITY   (United States)

Author keywords

cDNA synthesis; Peptidyl prolyl isomerase A gene; qRT PCR; Ribosomal protein L13 gene; Sf21 cells 28S rRNA; TATA box binding protein gene

Indexed keywords

COMPLEMENTARY DNA; PEPTIDYLPROLYL ISOMERASE; RIBOSOME PROTEIN; RIBOSOME PROTEIN 13; RNA 28S; TATA BINDING PROTEIN; UNCLASSIFIED DRUG;

ANALYTIC METHOD; ANIMAL CELL; ARTICLE; ASCOVIRUS; BACULOVIRUS; CONTROLLED STUDY; DNA SYNTHESIS; GENE AMPLIFICATION; GENETIC TRANSCRIPTION; HOUSEKEEPING GENE; INSECT CELL; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; REAL TIME POLYMERASE CHAIN REACTION; VIRUS INFECTION;

ANIMALS; BACULOVIRIDAE; CELL LINE; DNA PRIMERS; GENE EXPRESSION PROFILING; REFERENCE STANDARDS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, RIBOSOMAL, 28S; SPODOPTERA;

ASCOVIRUS; HEXAPODA;

EID: 73049108646     PISSN: 01660934     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jviromet.2009.09.019     Document Type: Article

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