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Signature motif of qnorB was identified by using PROSTIE (http://www.prosite.expasy.org/).org/
Heterogeneous elemental composition of bone was identified by using energy dispersive X-ray spectroscopy (EDS).
Microstructure was identified by using scanning electron microscopy and X-ray diffraction.
The ALL was identified by using a dissection technique that closely mimicked that of Caterine et al. [1].
The crystal structure of the primary grains was identified by using X-ray diffraction (XRD) (Figure 1B).
The bacterial 16S region, after amplification, was identified by using 5′-GATTAGATACCCTGGTAG-3′ and 5′-AGTCACTTAACCATACAACCC-3′ as primers.
M genitalium was identified by using validated polymerase chain reaction (PCR) primers, and the results were compared to pregnancy outcomes.
Individual hydrocarbon of oily bilge water was identified by using gas chromatography mass spectrometry (GC MS) analysis.
After hybridization, optimum probe sequence position was identified by using the differences between the responses of guanine oxidation signals.
The sequence obtained as described above was identified by using the NCBI BLAST program to run similarity searches against other sequences from available databases.
The first microbial hydrolysis of cyclo l-Asp-l-Asp) was identified by using Paenibacyclo l-Asp-l-Asp(DSM 329) and Rhizobium sp. NA04-01 (DSM 24917).
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