Sentence examples for tables were transferred from inspiring English sources

These selected tables were transferred and loaded into CDIS using the IBM DB2 database software.

Aliquots covering the working concentration ranges cited in Table 1 were transferred into 10-mL volumetric flasks.

Aliquots of MTP and FDP standard solutions covering the working concentration range cited in table 1 were transferred into a series of 10 mL volumetric flasks.

The resulting vectors pRH001-ptsP and -ptsO, -ptsOH30A and -ptsOS61A (Table S1) were transferred by mating into the ΔptsP or ΔptsO mutants to generate the complemented strains ΔptsP/ptsP, ΔptsO/ptsO, ΔptsO//ptsOH30A and ΔptsO/ptsOS61A.

All samples (Table 3) were transferred to Eppendorf tubes and centrifuged at 12,000 ×g for 5 min.

CT scans (n = 112, Table  1) were transferred to an open-source PACS workstation and DICOM viewer (www.osirix-viewer.com).

The resulting plasmids pCR018e to pCR024e (Table 4) were transferred into the corresponding mutant strains and the ability of the plasmid carrying strains to utilize inorganic sulphur sources was tested as described above.

Three microliters of diluted PCR product (dilutions in Table 1) were transferred in a mix of 15 μL of Hi-Di Formamide (Applied Biosystems) and 0.15 μL of GeneScan 500 LIZ Size Standard Applied BiosystemsStandard Applied Biosystems

The resulting plasmids pEPR1_prom_ cg0042 and pEPR1_prom_ cg2911 (Table 3) were transferred into the C. glutamicum ATCC 13032 wild-type strain and into the zur mutant C. glutamicum JS2502 to detect differential gfp expression by real-time RT-PCR, using high, low and chelated zinc conditions in the growth medium (Fig. 7).

Of the fifteen mutations identified in the 1974M1 mutant (Table 2), six mutations were transferred into both 1974T3 and R6T2 transformants (Table 2).

For experiments in Supporting Information, Table S2, whole pupae were transferred to microcentrifuge tubes and frozen at −80° 4–4.5 hr after they were irradiated as late third instar larvae.