ライフサイエンスコーパス: dilution series

1 monomolecular odor and then tested across a dilution series.

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

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

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

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

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

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

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

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

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

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

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

13 Using dilution series for validation, we demonstrate Pinnacle

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

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

16 An online calculator to create optimized dilution series is freely available at http://www.biokin

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

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

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

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

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

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

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

24 8 genome were evaluated for sensitivity with dilution series of DNA extracted from a cell line (BCBL-

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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