ライフサイエンスコーパス: 96-well plate format

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1 times as low as 15 s per sample based on the 96-well plate format.

2 This procedure was robust in a 96-well plate format.

3 te formation from alpha-ketoglutaramate in a 96-well plate format.

4 Arabidopsis thaliana) plants also grown in a 96-well plate format.

5 A substrate; the method was adapted to fit a 96-well plate format.

6 and typing of genital HPV using an automated 96-well plate format.

7 oate oligodeoxynucleotides in plasma using a 96-well plate format.

8 -throughput plasmid isolation system using a 96-well plate format.

9 tive, permitting high-content screening in a 96-well plate format.

10 continuous monitoring of ADO formation in a 96-well-plate format.

11 sposable-column format and a high-throughput 96-well-plate format.

12 yzes up to 32 samples in triplicate, using a 96-well-plate format.

13 erial solid-phase extractions performed on a 96-well plate format and are compatible with either IEX-

14 The procedure is applicable to both 96-well plate format and large-scale production of RNA.

15 They can live in 96-well plate format and readily absorb chemicals from t

16 que described here, BAC DNA is isolated in a 96-well plate format and simultaneously digested with fo

17 o screen for inhibitory small molecules in a 96-well plate format and use this to discover a new inhi

18 inhibitor dilutions within the context of a 96-well-plate format and simple serial dilution steps ar

19 T) activity in rat L6 skeletal muscle cells (96-well-plate format) and human skeletal muscle cells (2

20 d to conveniently monitor FDPS activity in a 96-well plate format, and that it can reproduce IC(50) v

21 sured as low as 3.55 +/- 1.84 fmols(-1) in a 96-well plate format, and the assay has been used to kin

22 measurement of luciferase luminescence in a 96-well plate format assay.

23 Multi-plexing sample preparation via a 96-well plate format becomes popular in recent years; ho

24 x labeling, pooling, and sample cleanup in a 96-well-plate format before reversed-phase liquid chroma

25 gometry assay, based on a readily accessible 96-well plate format coupled with quantification of sing

26 ons were utilized in a novel high-throughput 96-well plate format for drug metabolism profiling.

27 We used a 96-well plate format for plasmid purification, transform

28 Rapid screening of ligase fidelity in a 96-well plate format has allowed the study of ligase fid

29 The charcoal absorption method run in the 96-well plate format has general utility for any phospha

30 peed of the analysis was enhanced by using a 96-well plate format, portending applications in high-th

31 Here, we describe such a method in a 96-well plate format that is based on laser-induced poly

32 with a chemiluminescent readout adapted to a 96-well plate format, the effect of LEDGF/p75 on both th

33 s) for alpha-amino acids were conducted in a 96-well plate format to demonstrate the viability of the

34 Finally, the method is now performed in 96-well plate format using a benchtop orbitrap mass spec

35 ing an MMP-9 antibody and was performed in a 96-well plate format using a liquid-handling robotic pla

36 A fast screening assay in 96-well plate format was used to follow the enzymatic hy

37 e quenching technique is described here in a 96-well plate format which is capable of screening chemi

38 spiratory syncytial virus was developed in a 96-well plate format with a culture-confirmatory stain u

39 oaches, analysis of a set of samples using a 96-well plate format would take ~48 h: 1 h for system se

40 is protocol, the analysis of a sample set in 96-well plate format, would take ca. 30 h, including 1 h

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