R 15.4 cells. To do so, we designed a modified quantitative RTPCR (RT-qPCR). Our modified method, herein named RT-DNA-qPCR (RT-DqPCR), is based on the fact that molar ratio between two genes in genomic DNA is equal (see Supplemental text 1). In short, RT-DqPCR involves normalization of values obtained by amplification of cDNA to those obtained by amplification of genomic DNA with the same primer p

Ic? Findings from a population based study in Karachi, Pakistan. BMC Infect. Dis., 9, 38. http://dx.doi.org/10.1186/1471-2334-9-38 Fox, M. P., Mazimba, A., Seidenberg, P., Crooks, D., Sikateyo, B., Rosen, S. (2010). Barriers to initiation of antiretroviral treatment in rural and urban areas of Zambia: a cross-sectional study of cost, stigma, and perceptions about ART. J. Int. AIDS Soc., 13, 8. h

Infections using high level rhMBL (10 mg/ml) in 5 serum (i.e. diluted 20-fold). However, such a high concentration of rhMBL is considered supraphysiological if adjusted for the 20-fold dilution factor of serum. Although human MBL is produced primarily in the liver, extrahepatic MBL synthesis has been found in the gastrointestinal tract, middle ear fluid, and nasopharyngeal secretions. It is possi

R 15.4 cells. To do so, we designed a modified quantitative RTPCR (RT-qPCR). Our modified method, herein named RT-DNA-qPCR (RT-DqPCR), is based on the fact that molar ratio between two genes in genomic DNA is equal (see Supplemental text 1). In short, RT-DqPCR involves normalization of values obtained by amplification of cDNA to those obtained by amplification of genomic DNA with the same primer p

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