ライフサイエンスコーパス: total analysis

1 most negligible matrix effects, even for the total analysis.

2 ludes 12,678 individuals and 1.5 M SNPs, the total analysis can be run on a single desktop PC in less

3 The total analysis sample consisted of 30 230 respondents fr

4 izing molecular biological assays in a micro-total analysis system (muTAS) were developed for the det

5 method can be integrated into a microfluidic total analysis system composed of in-line DNA preconcent

6 fully integrated silicon/silica-based micro total analysis system for proteomics.

7 reaction and analysis steps to form a micro total analysis system.

8 Microscale total analysis systems (microTAS) allow high-throughput

9 We envision its use in mu-total analysis systems (mu-TAS) and in DNA-array chips u

10 cale can enhance the utility of miniaturized total analysis systems (mu-TAS).

11 Micro-total analysis systems (muTAS) have attracted wide atten

12 e for the development of droplet-based micro total analysis systems (muTAS).

13 etection of nucleic acids (NAs) within micro total analysis systems (muTASs) for point-of-care use is

14 With the rapid development of micro total analysis systems and sensitive biosensing technolo

15 ssibilities to design new compact disc-based total analysis systems applicable in chemistry and life

16 of microelectromechanical systems and micro total analysis systems requires many types of control.

17 y paves the way for the development of micro-total analysis systems that combine optical and impedime

18 results may lead toward the design of micro total analysis systems with microfluidics based on the r

19 systems for sample preparation in microscale total analysis systems, and improvements associated with

20 of this approach for integration into micro-total analysis systems, we optimized the production of a

21 wavelength-tunable light sources, and micro total analysis systems.

22 far afield, and future directions for micro total analysis systems.

23 ab-on-a-chip (LOC), microfluidics, and micro total analysis systems.

24 compounds was achieved within 16 min and the total analysis time (35 min) was ca. 3-fold shorter than

25 pounds was achieved in less than 3min with a total analysis time (sample-to-sample) of 10min.

26 curcuminoids in approximately 1.3 min with a total analysis time (sample-to-sample) of 7 min, includi

27 his microfluidic device, thus shortening the total analysis time and increasing the analysis throughp

28 oes not require a long extraction procedure (total analysis time can be lower than 30 min) and can be

29 per milliliter range can be attained, while total analysis time does not exceed 2 min per sample.

30 The total analysis time for a 6 mm (2) surface, which is lim

31 Using this system, the total analysis time for a 96-well microtiter plate has b

32 The total analysis time for the assay was less than 15 min.

33 Total analysis time including immunoassay was 22-32 min

34 ascorbic acid levels with less than a 15-min total analysis time including sample preparation and der

35 Total analysis time is <2 min, and the procedure is line

36 s with an excess of interfering DNA and in a total analysis time of 1 h and 30 min.

37 ere achieved using a capillary format with a total analysis time of 11 min.

38 et122, Met127, and Met138 oxidation within a total analysis time of 30 min.

39 ed characterization of the constituents in a total analysis time of 35 min.

40 separation was performed in 25.5 min, with a total analysis time of 35 min.

41 le platforms use just 50 muL of sample and a total analysis time of 360 s.

42 the minimum detection limit of 5.0pg/ml and total analysis time of 65min.

43 gration time precision less than 1% within a total analysis time of 9.0 min.

44 e carried out in diluted plasma samples in a total analysis time of 90 min.

45 to six different samples in parallel, with a total analysis time of about 60 min.

46 nly one set of oligonucleotide probes, for a total analysis time of less than 10 min post-PCR.

47 rforming as few as 10 thermal cycles, with a total analysis time of less than 20 min.

48 be identified over a healthy control with a total analysis time of less than 45 min.

49 For a total analysis time of less than 5 min, we estimate a ma

50 addition to the ultra-high sensitivity, the total analysis time of the assay is less than 3h, thus d

51 r the point-of-care detection of EVs, with a total analysis time of two hours.

52 on/analysis, and a duty cycle (percentage of total analysis time spent acquiring data) of 40% were ac

53 -CBS extractions at the same time allows the total analysis time to be reduced to less than 55 s per

54 ents in the experimental workflow allows the total analysis time to be shortened very significantly a

55 Improvements made to the workflow reduced total analysis time to less than 3 h.

56 yield improved signal-to-noise ratios with a total analysis time under 10 s.

57 x 10(6) cells/profile), and is rapid, with a total analysis time under 5 min/sample.

58 an 0.6% for intraday migration times and the total analysis time was less than 20 min.

59 ocessed using an off-line FISH protocol, the total analysis time was reduced from 2.5 h to 30 min.

60 The total analysis time with default parameters was less tha

61 l sample consumption of 270 ng in 120 min of total analysis time.

62 the detection of 71 impurities within 3 min total analysis time.

63 tter correction but at the expense of longer total analysis time.

64 e necessary for analysis and speeding up the total analysis time.

65 Using fHTCE, total analysis times can be reduced by up to 48% per mul

66 formed and completed every few seconds, with total analysis times of less than 10 min for tryptic pep

67 The total analysis times of less than 11 min provided limits

68 ential to increase sample throughput, reduce total analysis times, and increase signal-to-noise ratio

69 The total analysis was also enriched for melanoma-associated