ライフサイエンスコーパス: 3H-labeled

1 y excretion of the bile acid, taurocholate ([3H]-labeled; 1 micromol/min) and of the organic anion, b

2 .47L, which displayed a reduced affinity for 3H-labeled (1R,3R,4R)-3-[2-hydroxy-4-(1,1-dimethylheptyl

3 in or muscle contractions, measured with the 3H-labeled 2-N-4-(1-azi-2,2, 2-trifluoroethyl)-benzoyl-1

4 The affinity of 3H-labeled [2,3-dihydro-5-methyl-3-[(4-morpholinyl)methy

5 ncubated with 3H-mevalonolactone contained a 3H-labeled 28-kDa protein fraction.

6 mpanied by a proportional appearance in free 3H-labeled acetate in the assay mixture.

7 Recombinant fiber knobs and 3H-labeled Ad virions from serotypes representing all si

8 Isolated 3H-labeled alpha-chains are known to be degraded primari

9 Autoradiography confirmed accumulation of 3H-labeled amelogenin trityrosyl motif peptide in the re

10 and amino acid transport assayed by tritium (3H)-labeled amino acid uptake.

11 chiometry experiments, whereby the uptake of 3H-labeled amino acid and net inward charge were simulta

12 ]promegestone were irradiated at 312 nm, and 3H-labeled amino acids were identified by amino-terminal

13 iated (f0) H. influenzae type b 770235, were 3H labeled and overlaid on two-dimensional thin-layer ch

14 sis of product formed from [10R-3H] and [10S-3H]-labeled arachidonic acids revealed that 12R-HETE syn

15 trogen ICI 182780 on cellular degradation of 3H-labeled bone in vitro and on membrane HCl transport.

16 ostatin 1 in mice was undertaken, using [C26-3H]-labeled bryostatin 1.

17 tion-binding assays, A-204197 competed with [3H]-labeled colchicine for binding to tubulin (K(i) = 0.

18 By contrast, incubation of 3H-labeled des-Arg10-kallidin with cells expressing B1KR

19 The assay detects binding of 3H-labeled DNA to the bead-immobilized enzyme by scintil

20 Finally, using 32P- and 3H-labeled donor DNA, we demonstrate that a coiA mutant

21 The 3H-labeled enzyme retains its original NAD+/NADH content

22 engage in high-affinity, specific binding of 3H-labeled epibatidine (H-EBDN; macroscopic KD = 10 pM;

23 d that of other in vivo nAChR probes such as 3H-labeled epibatidine or norchloroepibatidine, [3H](-)-

24 lease levels were monitored by coincubating [3H]-labeled Escherichia coli ribosomal RNA with the expe

25 and 72 days after initial culture, uptake of 3H-labeled FDG, thymidine, L-methionine and L-leucine in

26 :1000 significantly inhibited the binding of 3H-labeled FN to C. tropicalis cells (P < .03).

27 ith Staphylococcus aureus V8 protease, and a 3H-labeled fragment was purified by reversed-phase high-

28 Almost all of the 3H-labeled HC neurons were found in a 350-m-wide layer o

29 nteract specifically with heparin-Sepharose, 3H-labeled heparin, or a heparin-bovine serum albumin co

30 parable amounts were compared, the number of 3H-labeled HVC neurons was 2.6 times higher in intacts t

31 ramatic age-related decline in the number of 3H-labeled HVC-RA neurons present 4 months after cell bi

32 d chromatography fraction containing a 28kDa 3H-labeled hydrophobic protein was collected, lyophilize

33 Studies using 3H-labeled IAA-phenylalanine showed that the uptake of c

34 A 3H-labeled inhibitor bound to full-length human iNOS mon

35 ld; there were no changes to levels of other 3H-labeled inositol phosphates.

36 mma) results in an increase in the uptake of 3H-labeled L-arginine and a concomitant increase in the

37 annose correction, we analyzed the amount of 3H-labeled LLO intermediates.

38 ase RIA, half-maximal binding of 5 microg/mL 3H-labeled LPS occurred at 5-10 microg/mL CAP18(106-138)

39 CB1 receptors and G-protein activation using 3H-labeled N-(piperidin-1-yl)-5-(4-chlorophenyl)-1-(2,4-

40 Within this layer the fraction of 3H-labeled neurons was 50% higher in juveniles than in a

41 y chromatography step was performed by using 3H-labeled nuclear proteins.

42 Most [3H]-labeled nuclei at 1-2 hr after [3H]-thymidine inject

43 Uptake of 3H-labeled oleate was significantly reduced in adipocyte

44 5 microM); however, it did not compete with [3H]-labeled paclitaxel.

45 as examined by labeling of the protein with [3H]-labeled palmitic acid.

46 3H-labeled palmitoylated alpha-tubulin was cleaved with

47 LH60 and dual sequencer runs, positioned the 3H-labeled palmitoylated amino acid residues in peptides

48 The position of 3H-labeled palmitoylated amino acids in peptides could n

49 ne for sequence analysis and one to identify 3H-labeled palmitoylated amino acids.

50 ivative, identified the cycle containing the 3H-labeled palmitoylated residue.

51 3H-Labeled peptides eluted from B27 molecules of lymphob

52 mixtures of PLTP and the vesicles containing 3H-labeled phosphatidylcholine and 14C-labeled cholester

53 osure to ionomycin also led to an efflux of [3H]-labeled protein, amounting to 41% of the labeled pro

54 cytes expressing T8, Na+-dependent uptake of 3H-labeled purine (adenosine, inosine, and guanosine) an

55 onary sinus plasma were quantified by use of 3H-labeled radioenzymatic assay in 8 open-chest, anesthe

56 3) FX activation peptide region was 3H-labeled; release of 3H was used to measure FXase acti

57 Only bound 3H-labeled RNA transcripts are brought in close enough p

58 3H-labeled RNA transcripts are hybridized in solution to

59 This is followed by an incubation with 3H-labeled SAM and SssI methyltransferase for methylatio

60 h pressure liquid chromatography analysis of 3H-labeled species released from [3H]adenine-loaded HNE

61 tified by the measurement of the adhesion of 3H-labeled Streptococcus sanguis to saliva-conditioned s

62 ffect kH/kT = 1.27 +/- 0.03 for [1(R)-2H,(S)-3H]-labeled substrate in D2O is subtantially larger than

63 when intact neurons were pulse-labeled with 3H-labeled sugars at low temperature or after treatment

64 Use of [3H]-labeled TPCK showed that inactivation was associated

65 3H-Labeled type IV human collagen incorporated in the Ma

66 ned by zymography and in situ degradation of 3H-Labeled type IV human collagen.

67 ntitates the radioactivity incorporated from 3H-labeled UDP-GalNAc into a biotin-labeled acceptor pep