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Infant genotyping of CCR2-64I and CCR5 promoter polymorphisms were determined using a multiplex ligase detection reaction (LDR) based method with flow cytometric technology, previously described [43], [44].
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Genetic identification of enterococci to species level and detection of vanA, vanB, vanC1, or vanC2/C3 and vanD ligase genes were performed by using a multiplex polymerase chain reaction amplification (7 ).
Using a multiplex PCR assay, X. oryzae pv.
SCCmec type assignment was performed using a multiplex PCR method, as described previously [22].
Cytokines were measured using a multiplex sandwich-ELISA assay (Aushon Biosystem, Billerica, MA).
cDNA was synthesized from total RNA using a Multiplex RT for Taqman array kit (Applied Biosystems, Foster City, CA).
Genotyping was performed using a multiplex protocol (see Supporting Information).
Molecular serotyping was completed using a multiplex PCR scheme [ 61].
Target DNA sequences were amplified using a multiplex PCR method and ligation reactions for each subject were carried out in a final volume of 10 μL containing 1 μL of 10× buffer, 100 ng of multi-PCR product, 1 pmol of each discriminating oligo, 1 pmol of each common probe, and 2 U of Taq DNA ligase (New England Biolabs, Beverly, MA, USA).
IL-6 was measured using a multiplex panel (BioRad).
Plasma samples were analysed using a multiplex ELISA.
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