ライフサイエンスコーパス: sodium dithionite

1 action with strong reducing reagents such as sodium dithionite).

2 ectron-reduced species during titration with sodium dithionite.

3 ted by treating cells with sodium sulfite or sodium dithionite.

4 of outer leaflet probe with externally added sodium dithionite.

5 lipid with the membrane-impermeant reductant sodium dithionite.

6 intramolecular reductive amidation employing sodium dithionite.

7 over the course of reductive titrations with sodium dithionite.

8 nd then exposed to the hemoprotein reductant sodium dithionite (1 mmol/L) under N(2), there is a part

9 nverted to the reduced form upon addition of sodium dithionite and hydrogen.

10 reductive titrations of CODH/ACS with CO and sodium dithionite and monitored the reaction by electron

11 Reduction of the mutant with sodium dithionite and reoxidation with Me(2)SO, however,

12 ve titrations with both the 1-electron donor sodium dithionite and two-electron donor NADPH demonstra

13 lates transiently during both reduction with sodium dithionite and with NADH in the presence of catal

14 The diferric cluster could be reduced by sodium dithionite, and the diferrous state was found to

15 nes were next reduced to aminotyrosines with sodium dithionite, and-at pH 5.0-cleavable biotin tags w

16 d pterin-free iNOS(heme) was examined, using sodium dithionite as the reductant.

17 rates greatly exceeding those observed with sodium dithionite assays.

18 n assays containing SAM, BChlide c or d, and sodium dithionite, BciD catalyzed the conversion of SAM

19 d-type PS I, reduction of F(A) and F(B) with sodium dithionite causes a approximately 30% increase in

20 m to the wild-type protein and is reduced by sodium dithionite, demonstrating that it is a flavin-bin

21 Additional sodium dithionite first produces some neutral, blue flav

22 NT is reduced to 3-aminotyrosine (3AT) using sodium dithionite followed by derivatization of light an

23 bated with GTP, S-adenosyl-L-methionine, and sodium dithionite in the absence of MoaC.

24 After reduction with sodium dithionite in the presence of light, approximatel

25 here that when a HbRC core is incubated with sodium dithionite in the presence of light, the 15 ms ch

26 Reductive titration with sodium dithionite indicates heme reduction takes place p

27 In contrast, proline and sodium dithionite induce tight binding of PutA to the li

28 Sodium dithionite is added subsequently to reduce the ni

29 (4a H)-diones to xanthones by treatment with sodium dithionite is described.

30 din to emodin hydroquinone, for example with sodium dithionite, is obligatory for the enzymatic reduc

31 obic reduction of the ferric-NO species with sodium dithionite led to the formation of two spectrally

32 Our study shows that sodium dithionite, most likely due to its decomposition

33 othiadiazine-1,1-dioxides in the presence of sodium dithionite (Na(2)S(2)O(4)) is reported under mild

34 s impeded olivine dissolution; however, with sodium dithionite (Na(2)S(2)O(4)), a reducing agent, oli

35 Sodium dithionite (Na(2)S(2)O(4)), lowering pO(2) to 10

36 rated in situ from the reagents rongalite or sodium dithionite (Na(2)S(2)O(4)), was found to be the k

37 ncreased when [Ca2+]o was doubled.Hypoxia by sodium dithionite (Na2S2O4) induced large [Ca2+]i increa

38 Reduction of the Hox sample with 100% H2 or sodium dithionite (NaDT) nearly eliminated the 2.1 signa

39 e presence of the nonphysiological reductant sodium dithionite (NaDT), is believed to play a crucial

40 Reduction with either sodium dithionite or dithiothreitol decreased the copper

41 In the presence of sodium dithionite or in the presence of P. aeruginosa fe

42 itrations show that approximately 1 equiv of sodium dithionite or NADPH is required to fully reduce C

43 Anaerobic reduction of the enzyme with sodium dithionite or substrate yields no detectable semi

44 ls and treating them with the reducing agent sodium dithionite prior to EPR measurements.

45 Reduction of this RRE reaction product with sodium dithionite produces the one-electron-reduced RRE,

46 When sodium dithionite-reduced LipA was incubated with octano

47 Under H2 or sodium dithionite reductive treatments, the EPR spectra

48 Titration of the FMN domain with sodium dithionite resulted in the conversion of the prot

49 Reduction of emodin by sodium dithionite resulted in the formation of two tauto

50 ctants, and anaerobic reduction of BioB with sodium dithionite results in conversion to enzyme contai

51 Reduction with sodium dithionite results in small quantities of an S =

52 tion of the TMADH x ETF protein complex with sodium dithionite shows that a total of five electrons a

53 er, we confirm that it is the reducing agent sodium dithionite that facilitates release of CO from th

54 y incubating such a crystal in a solution of sodium dithionite, the reductive cleavage of SAM is trig

55 Compared with the commonly used reductant sodium dithionite, this work shows that Eu(II) can serve

56 When BMR is titrated with NADPH or sodium dithionite under anaerobic conditions, addition o

57 nt with either sulfide or bisulfite, or with sodium dithionite under weakly acidic conditions in the

58 n greatly increases the rate of reduction by sodium dithionite when compared to pentacoordinate hemog

59 e of CO in protein solutions alone i.e. when sodium dithionite, widely used in previous studies of CO

60 The use of sodium dithionite with perfluoroalkyl iodides under basi