Identification of normalization factors for quantitative real-time RT-PCR analysis of gene expression in Pacific abalone Haliotis discus hannai
Author:
Publisher
Springer Science and Business Media LLC
Subject
Water Science and Technology,Oceanography
Link
http://link.springer.com/content/pdf/10.1007/s00343-013-2221-0.pdf
Reference42 articles.
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3. Bas A, Forsberg G, Hammarstrom S, Hammarstrom M L. 2004. Utility of the housekeeping genes 18S rRNA, betaactin and glyceraldehyde-3-phosphate-dehydrogenase for normalization in real-time quantitative reverse transcriptase-polymerase chain reaction analysis of gene expression in human T lymphocytes. Scand. J. Immunol., 59(6): 566–573.
4. Bustin S A. 2002. Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems. J. Mol. Endocrinol., 29(1): 23–29.
5. Cai J, Li J, Thompson K D, Li C, Han H. 2007. Isolation and characterization of pathogenic Vibrio parahaemolyticus from diseased post-larvae of abalone Haliotis diversicolor supertexta. J. Basic. Microb., 47(1): 84–86.
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