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S Tac1p regulon. Eukaryot Cell 2007, 6:2122-2138. 53. Znaidi S, Barker KS, Weber S, Alarco AM, Liu TT, Boucher G, Rogers PD, Raymond M: Identification of the Candida albicans Cap1p regulon. Eukaryot Cell 2009, 8:806-820. 54. Lu TK, Collins JJ: Dispersing biofilms with engineered enzymatic bacteriophage. Proc Natl Acad Sci USA 2007, 104:11197-11202. 55. Wang X, Preston JF, Romeo T: The pgaABCD locu
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S Tac1p regulon. Eukaryot Cell 2007, 6:2122-2138. 53. Znaidi S, Barker KS, Weber S, Alarco AM, Liu TT, Boucher G, Rogers PD, Raymond M: Identification of the Candida albicans Cap1p regulon. Eukaryot Cell 2009, 8:806-820. 54. Lu TK, Collins JJ: Dispersing biofilms with engineered enzymatic bacteriophage. Proc Natl Acad Sci USA 2007, 104:11197-11202. 55. Wang X, Preston JF, Romeo T: The pgaABCD locu
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Supernatant, which served as an extraction and inhibition control agent, before nucleic acid was extracted using the CAS1820 XtractorGene automated system (Qiagen-Australia) according to the manufacturer's instructions. The final volumes of specimen extracts were 150 L/specimen eluted in 96 well racks (Matrix, Thermo Scientific, Australia). For each run (96 extracts/run), extracts were tested usin
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Supernatant, which served as an extraction and inhibition control agent, before nucleic acid was extracted using the CAS1820 XtractorGene automated system (Qiagen-Australia) according to the manufacturer's instructions. The final volumes of specimen extracts were 150 L/specimen eluted in 96 well racks (Matrix, Thermo Scientific, Australia). For each run (96 extracts/run), extracts were tested usin
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He first year mould was seen in some samples as they arrived in the laboratory and we became concerned about the impact of this contaminant upon sample integrity. Therefore, as part of the ORChID study, we undertook a broader investigation of sample quality, examining collection and transportation, and how these impact on respiratory virus detection. Our objectives were first to determine the qual
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T tube that contained a viral transport media-soaked foam pad in the base. Parents were instructed to squeeze the foam pad to release the fluid and bathe the top of the swab. Ideally within 24hours of collection, the nasal swabs were then sent byAlsaleh et al. BMC Infectious Diseases 2014, 14:15 http://www.biomedcentral.com/1471-2334/14/Page 3 ofregular postal mail (in accordance with Australia Po
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Eir infant's second birthday. Instructions on sample collection were provided at the initial visit by research staff who also demonstrated the technique by undertaking the initial nasal swab specimen shortly after delivery of the newborn baby. In addition, parents were given written instructions on how to collect nasal swab specimens. They also received regular text messages, emails or telephone c
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Eir infant's second birthday. Instructions on sample collection were provided at the initial visit by research staff who also demonstrated the technique by undertaking the initial nasal swab specimen shortly after delivery of the newborn baby. In addition, parents were given written instructions on how to collect nasal swab specimens. They also received regular text messages, emails or telephone c