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1 ter the substrate has been precipitated with trichloroacetic acid).
2 , commonly used alcohols, and mild acids (5% trichloroacetic acid).
3 f the deblocking reagent prepared from solid trichloroacetic acid.
4 er of silicone oil into a denser solution of trichloroacetic acid.
5 ter clarifying the sample by the addition of trichloroacetic acid.
6 hrome P450Betamicro-3 was accomplished using trichloroacetic acid.
7 self-aggregating, acidic, and soluble in 5% trichloroacetic acid.
8 s are driven by aliquots of a chemical fuel, trichloroacetic acid.
9 preparation was performed by extraction with trichloroacetic acid 5% and solid phase extraction clean
12 Two other methods of precipitating proteins (trichloroacetic acid and phenol-ether) both exhibited va
14 methanol, acetonitrile, perchloric acid, and trichloroacetic acid and ultrafiltration approaches usin
15 cluding ultrafiltration, precipitation using trichloroacetic acid, and a direct in vivo measurement b
16 Prior to MSPE, the sample was treated with trichloroacetic acid, and the APs derivatized with aceti
17 mide, the protein was then precipitated with trichloroacetic acid, and the precipitate was separated
18 The metabolites released by extraction with trichloroacetic acid are recovered and quantitatively de
23 ogenesis or mere carbon exchange between the trichloroacetic acid cycle and the gluconeogenic pathway
24 conclude that at least 2 HAAs (dichloro- and trichloroacetic acids, DCAA and TCAA) are always present
28 oxyl-[32P]CoA followed by precipitation with trichloroacetic acid indicates that inactivation correla
30 raction of malonyl-CoA from tissue using 10% trichloroacetic acid, isolation using a reversed-phase s
32 gels can be rapidly visualized by soaking in trichloroacetic acid or chloroform followed by illuminat
36 thesis using (3)H-proline incorporation into trichloroacetic acid-precipitable material and for glyco
37 by this digestion, but only about 10% of the trichloroacetic acid-precipitable material was released
38 ion of 14C-labeled NeuAc from CMP-NeuAc into trichloroacetic acid-precipitable material when the lst
39 oid gland and its appearance in the serum as trichloroacetic acid-precipitable radioactivity was grea
41 asured by o-phthaldialdehyde derivatization, trichloroacetic acid precipitation and hydrochloric acid
42 H]UDP-GlcNAc from 3H-p62ST acceptor peptide (trichloroacetic acid precipitation and metal-chelation a
43 the medium remained intact, as determined by trichloroacetic acid precipitation and SDS/PAGE, and aft
47 el electrophoresis (SDS-PAGE) but only after trichloroacetic acid precipitation; heating to 95 degree
48 oxidative metabolites, median predictions of trichloroacetic acid production were less variable (2-fo
49 acids and related compounds by perchloric or trichloroacetic acid results in the formation of methylg
53 ted CFTR could be subsequently degraded into trichloroacetic acid-soluble fragments upon incubation i
54 her by the degradation of 125I-labeled OS to trichloroacetic acid-soluble label or by the cleavage of
58 otein degradation was examined by release of trichloroacetic acid-soluble radioactivity from cells pr
60 imultaneously carried out by the addition of trichloroacetic acid (TCA) and subsequent centrifugation
62 formats (macro-, micro-, and nanoassay) with trichloroacetic acid (TCA) as protein precipitating agen
63 s obtained for dichloroacetic acid (DCA) and trichloroacetic acid (TCA) in methylene chloride were fo
64 ived from rHag B-immunized rats reacted with trichloroacetic acid (TCA) precipitates of P. gingivalis
67 -urea, thiourea/urea, phenol, and a modified trichloroacetic acid (TCA)/acetone-to determine their ef
68 and by measuring maternal urinary levels of trichloroacetic acid (TCAA) during early pregnancy in a
71 tic acid (MBAA), dichloroacetic acid (DCAA), trichloroacetic acid (TCAA), and summary DBP measures (H
72 studied in drinking water exposure included: trichloroacetic acid (TCAA), monochloroacetic acid (MCAA
73 n kinetics of dichloroacetic acid (DCAA) and trichloroacetic acid (TCAA), the two predominant HAA spe
74 nly the analysis of PLP requires mixing with trichloroacetic acid to release the protein-bound vitami
78 tic, tribromoacetic, chlorodibromoacetic and trichloroacetic acid were the major HAAs components.
79 pha-chloro-substituted acetic acids, such as trichloroacetic acid, which are widely and successfully
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