Sentence examples for used for inserting from inspiring English sources

The location where the thinnest subcutis is expected is best used for inserting the Veress needle or trocar.

This tubular test assembly incorporates ten rigs of about 200 cm length used for inserting instrumented test capsules with miniaturized specimens taking advantage of the 'small specimen test technology'.

The DNA coding for crtW was inserted into the Sfu I and EcoR I restriction sites of plasmid pGAPZαA, and the same restriction sites were used for inserting crtZ DNA into pGAPZαA*.

Oligonucleotides used for inserting the region coding for a 6-His tag at the amino-terminal end of the mature PilC protein were: C1N-HIS-APA (5'-GGG CCC AGG CGCA AAC CCA TCA CCA CCA TCA TCA CAG TAA ATA CGC TAT TAT CAT GAA CGA A-3'), C2N-HIS-APA (5'-GGG CCC AGG CGC AAA CCC ATC ACC ACC ATC ATC ACA ACA CCT ATC CAT ACG TTA TTG TAA TG-3'), and CR328BsiWI (5'- GAA ACC TTG CCG TAC GGC GGC AGG TAG GTAG').

The diagonal matrix (after decomposition on SVD) S is used for inserting the watermark after decomposition on wavelet transform.

Primers used for inserting the (GS 8 linker into the Doc domain: Fw 5'-ggttctggctccggttctggctccagcatcaacactgacaat-3' Rev 5'-agaaccggagccagagccggaacctatacctgatctcaaaacatatct-3' Fusion proteins HIS-CBM A2C-Coh2 (C.t).

To further verify that the BAC library we constructed contained pine genomic DNA inserts, one of the gels used for insert size determination was transferred to a nylon membrane and probed with labeled pine genomic DNA as described previously [58].

As a result, the PCR-primers used for insert DNA generation remain short, minimizing the chance for secondary structure and primer-dimer formation as well as synthesis errors to occur.

Cultures of transformed E. coli were grown over-night in 100 ul LB media containing 100 ug/ml ampicillin, the cells were centrifuged and suspended in sterile distilled water, heat denatured for 10 mins at 95°C, 1 ul of supernatant was used for insert amplification with M13 forward and reverse primers.

PCR2 products were purified using QIAquick Gel Extraction Kit (QIAGEN) before used in TOPO Cloning, which is a blunt end subcloning used here for inserting the full-length synthetic genes into the pCR-Blunt II-TOPO vector for amplification and DNA sequencing.

Only 1 out of 287 dual-mobility cups investigated in our study was revised due to dislocation, although this implant was mostly used for THA inserted because of femoral neck fracture.