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Objectives: A new approach for the diagnosis of enterovirus infections was performed, using the reference strain inferred from sequence analysis of PCR products.
Quality control was routinely performed during DST using the reference strain H37Rv (ATCC27294).
First, the spectral database was set up using the reference strain set.
Prior to using the reference strain for manufacturing vaccines, it should meet these characteristics when checked according to standard protocols.
Haemagglutination inhibition (HI) was performed at NIC to measure pH1N1-specific antibodies by as described previously [ 14], using the reference strain A/California/7/2009.
The MIRU-VNTR 24-loci profiles and spoligotyping patterns were used to classify the strains into main phylogenetic lineages by using the reference strain collection and identification tools available online at http://www.miru-vntrplus.org[ 21].
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Quality control was routinely performed during DST using the reference strains provided by the National Institute for the Control of Pharmaceutical and Biological Products (China).
The phylogenetic analysis described here was carried out by using the reference strains of all available Pristionchus species (Table 1).
Quality control was performed during susceptibility testing using the reference strains provided by the National institute for the control of pharmaceutical and biological products (China).
Duplicates were assigned to these bins using the reference strains S288c (S. cerevisiae) and CBS432 (S. paradoxus) with Blast-like alignment tool (Kent 2002).
Using the reference strains NineMile RSA493 (GenBank: AE016828), Henzerling, and Priscilla Q177, five separate PCR assays where established and optimised for each target (Table 3).
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using the reference signal
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using the yeast strain
using the reference book
using the reference sample
using the reference map
using the reference symbol
using the reference flow
using the reference tracer
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