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) strain to determine the calibration curve that the liquid chromatography device could determine the additional samples parasite number in copy numbers. PCR products were purified with PCR Clean up-M Kit (Viogene, Sunville, CA). The sequence of

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Physiology International
Authors: E Bulut, G Öztürk, M Taş, MT Türkmen, ZD Gülmez, and L Öztürk

, Hatfield, UK). Proper-sized adult probes that ensure a tight seal in the ear canal were used. The probe was calibrated using the 1 cc acoustic calibration cavity. Broadband noise was used as the CAS. Test probes were placed into both ear canals and linear

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Journal of Behavioral Addictions
Authors: Sawitri Assanangkornchai, Edward B. McNeil, Nopporn Tantirangsee, Phunnapa Kittirattanapaiboon, and Thai National Mental Health Survey Team

weights calculated from the multistage sampling study design. Post-stratification calibration was used to adjust the sampling weights based on the non-response and the age and sex distribution of the Thai population. Ethics

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Acta Microbiologica et Immunologica Hungarica
Authors: Joana Korabliovienė, Mykolas Mauricas, Česlova Ambrozevičienė, Mindaugas Valius, Algirdas Kaupinis, Saulius Čaplinskas, and Pavel Korabliov

calibration purpose. Data processing, searching, and analysis Raw data files were processed and searched using ProteinLynx Global SERVER (PLGS) version 3.0.1 (Waters Corporation). Mycobacterium protein sequence database

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provided the Aix. CSBP was directly calculated from the carotid pulse waveform using the calibration considering brachial systolic and diastolic blood pressures. Epidemiologic and Laboratory data Baseline data on current

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concentrations of the peptide were calculated with the help of a calibration curve [ 15, 16 ]. The ‘‘ab35342’’ (Abcam, Cambridge, UK) PACAP38 antiserum was raised in sheep against the synthetic peptide (human) conjugated to keyhole limpet hemocyanin. The

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Acta Microbiologica et Immunologica Hungarica
Authors: Tamás Gáll, Gábor Lehoczki, Gyöngyi Gyémánt, Tamás Emri, Zsuzsa M. Szigeti, György Balla, József Balla, and István Pócsi

. Spectra from multiple (at least 100) laser shots were summarized using 19-kV accelerating and 20-kV reflectron voltage. External calibration was applied using the [M  +  Na]  +  peaks of cyclodextrins degree of polymerization 6–8 with m / z : 995 Da, m

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. Sphinganine and sphingosine levels were determined by LC-MS. Chromatographic separation was carried out using a Waters Symmetry C 18 column (150 mm × 2.1 mm, ID 5 µm; Waters, Mildford, MA, USA). Quantitative measurement was based on linear calibration to

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metalloproteinase-9 (MMP-9) ( 25 ) were determined using commercial ELISA kits. The procedures for all biochemical assays were performed as described in the product manuals. The results were estimated from the standard calibration curves on the internal standards

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II isokinetic device (Mechatronic Ltd., Szeged, Hungary) with a sampling frequency of 1,000 Hz was used for measuring hamstring and quadriceps torques. Special details of the device and its calibration have been described previously ( 44 ). Subjects

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