ライフサイエンスコーパス: dilution series

1 amplification curves for all reactions in a dilution series.

2 monomolecular odor and then tested across a dilution series.

3 sion, and ability to detect differences in a dilution series.

4 itive samples are subsequently analyzed as a dilution series.

5 h the hanging drop behavioral assay, using a dilution series.

6 We compared the HIV-1 load results for a dilution series (1 to 5 nominal log(10) copies/ml) and 1

7 ported in copies per milliliter by analyzing dilution series and clinical plasma samples by both meth

8 A and PEMAX reduced PCR-detected Mtb DNA for dilution series and Cohort A sputum versus untreated con

9 normal mammary epithelial cells (MECs) in a dilution series and inoculated into epithelium-free mamm

10 sample, which was subject to a 2- to 16-fold dilution series and run by UPLC coupled to time-of-fligh

11 om different pairs of species was mixed in a dilution series and species-specific RPL19 primers were

12 nd to keep a constant mixture composition in dilution series and throughout test duration.

13 We propose a simple, systematic dilution series approach where by the first dilution is

14 First, a sequential 2-fold dilution series containing equal amounts of gene-specifi

15 arrays use parametric response curves fit to dilution series data.

16 ence decrease of positive probes over a 1:10 dilution series demonstrated semiquantitative measuremen

17 el consisted of 24 coded samples including a dilution series for HPV types 16 and 18, alone or in com

18 Using dilution series for validation, we demonstrate Pinnacle

19 ntial design of experiments (DoE) based on a dilution series from a pooled sample and a measure of co

20 assayed by the intracerebral inoculation of dilution series into healthy weanling hamsters, which we

21 imulation study confirmed that the optimized dilution series is significantly more efficient than the

22 assay sensitivity was assessed with a serial dilution series of 10(-)(7) to 10(-)(1)(0) of vCJD prion

23 A calibration curve was prepared with a dilution series of a cloned human anti-ADAMTS13 autoanti

24 A dilution series of a HeLa tryptic digest (5-0.05 ng/uL)

25 y surfaces of CAII and analyzed an identical dilution series of acetazolamide (ranging from 4.1 to 10

26 The panel included a dilution series of an early convalescent human serum, kn

27 Subsequently, we performed a dilution series of an iTTP plasma sample for the multipl

28 We showed that applying a dilution series of calibration standards followed by a h

29 Here we demonstrate, through a dilution series of cDNA derived from 10 micro g of total

30 rtners could be measured directly by using a dilution series of cell lysates containing FRET hybrids,

31 In the serum sensing assay, a dilution series of cell media containing different conce

32 easures of assay performance were evaluated: dilution series of confirmed positive and negative sampl

33 8 genome were evaluated for sensitivity with dilution series of DNA extracted from a cell line (BCBL-

34 Finally, separate dilution series of HMPV A and B lineages were used to fu

35 cale enables interaction screening against a dilution series of immobilized proteins on the microarra

36 A dilution series of individual concentrations sprayed ove

37 The model was validated on an independent dilution series of patient plasma.

38 for in-gel protein digests, using a standard dilution series of phosphorylase B and carbonic anhydras

39 nearity were characterized by constructing a dilution series of photon-upconversion nanoparticles.

40 se (Gmd) domain, and subsequent testing with dilution series of pooled positive human serum confirmed

41 an 1 order of magnitude, demonstrated with a dilution series of the compound mixture, using robust an

42 To validate the assay, we screened a 7-point dilution series of the LOPAC 1280 library collection and

43 A dilution series of the proteases was used to determine t

44 The study design is based on a dilution series of two human tissues (blood and placenta

45 mplex (Mtb) qPCR, Xpert MTB/RIF] was done on dilution series of untreated and treated (PMA, PEMAX, DN

46 ant L+D-lipid concentrations yield a surface dilution series of variable L-lipid concentration with c

47 Using expressed RNA and 10-fold dilution series of virus-infected tissue culture isolate

48 Test samples included two separate dilutions series of plasma samples from experimentally i

49 automatically generating a two- or threefold dilution series (of seven or five concentrations, respec

50 Dilution series produced the expected pattern of dose-re

51 ssay run with plasma on clinical samples and dilution series (R(2) = 0.71 and 0.99 respectively).

52 The dilution series ranged from <100 to 5,000,000 HCV RNA co

53 ons into a 384-well plate, the 2-fold serial dilution series required for broth microdilution testing

54 he direct DNA extraction from urine samples (dilution series spiked in human urine).

55 roperties were indeed invariant in a surface dilution series, supporting rationale (ii), and were use

56 ng avidity of rIgG1 was measured by modified dilution series technique and surface plasmon resonance.

57 ered silver nanoparticles), we show how this dilution series technique improves resolution of the par

58 ration estimation at the level of individual dilution series to account for within-sample or within-g

59 al assays performed on all wells of doubling dilution series to determine MICs.

60 diluted successively multiple times, forming dilution series to extend the dynamic range of the measu

61 erformed comparative proteomic analysis of a dilution series using CE and nanoflow liquid chromatogra

62 y testing protocol utilizing a predetermined dilution series was used to evaluate each assay, enablin

63 ed on evaluation of the linear response to a dilution series, was used as a parameter for the assessm

64 Using synthetic peptide dilution series, we show that the sensitivity, dynamic r

65 quantification, the mimetic tissue model and dilution series, were used to quantify clozapine and its

66 normalization had a larger influence on the dilution series, where the use of the internal standard

67 d on bacterial growth in antibiotic doubling dilution series, which means that any error in the refer

68 n ([I]=0, 0.5[E]0, and [E]0), using a narrow dilution series with only two or three points to determi

69 The method used a sorbent dilution series with solid supported lipid membranes (SS