ライフサイエンスコーパス: o-phenanthroline

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1 ferent organic complexing ligands, EDTA, and o-phenanthroline.

2 ion +5 with the chemical cleavage agent 1,10-o-phenanthroline.

3 nucleases are inhibited by the zinc chelator o-phenanthroline.

4 m the growth medium with the chelating agent o-phenanthroline (20 microM) mimics aerobiosis or combin

5 o-Phenanthroline (250 microM), a selective chelator of F

6 N-acetylcysteine and o-phenanthroline abolished ERK activation by BHTOOH, con

7 In the presence of o-phenanthroline, an inhibitor of mitochondrial processi

8 The metal was complexed with o-phenanthroline and eosin at pH 7.5 in Tris; a piece of

9 ited by metal ion chelators such as EDTA and o-phenanthroline and partially inhibited by myxothiazol

10 ter by Cu(II) neocuproine (compared with the o-phenanthroline and terpyridine complexes) better allow

11 peptide libraries was completely blocked by o-phenanthroline and thus required metallopeptidases.

12 sensitivity to inhibition of DNA binding by o-phenanthroline, and immunological properties of the li

13 ic RNA cleavage when compared with analogous o-phenanthroline- and terpyridine-derived reagents.

14 environment, when complexed with Cu2+, 1,10-o-phenanthroline causes cleavage of nearby nucleic acids

15 We have linked the DNA cleaving moiety o-phenanthroline-copper to eight different sites within

16 Moreover, in the presence of o-phenanthroline-copper, a Cys residue at position 42 in

17 is study utilizes a chemical nuclease, 1, 10-o-phenanthroline-copper, to localize regions of 16S rRNA

18 d p-phenanthroline inhibit import similar to o-phenanthroline, indicating that inhibition of import i

19 High concentrations of EDTA and o-phenanthroline inhibit import of iron-sulfur protein i

20 of the cleavage reagent 5-iodoacetamido-1,10-o-phenanthroline (IoP).

21 Pharmacological inhibition of Rpn11 with O-phenanthroline (OPA) blocks cellular proteasome functi

22 p56(lck) dimers with the Zn2+ chelators 1,10-O-phenanthroline or 8-hydroxyquinoline-5-sulfonic acid r

23 pretreatment with either N-acetyl-cysteine, o-phenanthroline, or mannitol, indicating that metal-cat

24 ation of actin monomer (G-actin) with copper o-phenanthroline resulted in a rapid, high yield of disu

25 The Zn2+ chelator o-phenanthroline reverses the blockade.

26 Conversely, o-phenanthroline reversibly impaired the PS-direct of ac

27 In the presence of o-phenanthroline, S-nitrosocysteine decomposition follow

28 were degraded rapidly by a process involving o-phenanthroline-sensitive metallopeptidases.

29 inhibited by the zinc-chelating agent, 1,10-o-phenanthroline, suggesting it might be a zinc finger p

30 ytic processing of the presequence, and that o-phenanthroline together with EDTA inhibits import of i

31 The inhibitory effects of o-phenanthroline were related to suppression of S-nitros

32 bited by the same concentrations of EDTA and o-phenanthroline which inhibit import of the wild-type p

33 In addition, the effects of o-phenanthroline (which removes Ni but not Cu) and neocu

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