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1 ng platelets as identified by the binding of thiazole orange.
2 e-based cationic core structure identical to thiazole orange.
3 By covalently incorporating modifications of thiazole orange-a known DNA-intercalating fluorophore-in
4 was designed and synthesized on the basis of thiazole orange and isaindigotone skeleton.
5 hain antibodies (scFvs) using derivatives of thiazole orange and malachite green.
6  was used to measure RPs after staining with thiazole orange and to define the upper 20% and lower 20
7  functional groups including biotin, BODIPY, thiazole orange, and Cy7 through a polyethylene glycol l
8 icity, charge, and size (acridine, psoralen, thiazole orange, and phenanthridine) produced DISHs with
9 en tethered to the intercalating fluorophore thiazole orange, and the DNA recognition characteristics
10                     We determine, using this thiazole orange assay on a crude bacterial cell lysate,
11 ) series of aptamers were selected to bind a thiazole orange based (TO1-Biotin) ligand.
12 quadruplex formation of c-di-GMP to design a thiazole orange-based fluorescent detection of this impo
13  were conjugated to a DNA-intercalating dye, thiazole orange, by a reaction targeting Cys 110 of hist
14 e molecules of DNA multiply labeled with the thiazole orange derivative T06 as they passed through th
15      Specifically, we have developed a novel thiazole orange derivative, TOR-G4, that exhibits a uniq
16 ide probes were doubly labeled with adjacent thiazole orange derivatives.
17 NA) probes in labeling mRNA transcripts with thiazole orange donor and Alexa-594 acceptor fluorophore
18 5'-WGWWCW-3' (W = A or T) were conjugated to thiazole orange dye at the C-termini to examine their fl
19             We synthesized two conjugates of thiazole orange dye to small molecules (GMP and AMP) and
20 from the displacement of ethidium bromide or thiazole orange from the DNA of interest or, in selected
21                                          The thiazole orange is able to intercalate and fluoresce whe
22                                              Thiazole orange is also shown to oxidize the 5'-G of rem
23 he quinolinium ring system (SYBR Safe, n-Pr; thiazole orange, Me).
24  the recognition sequence where the tethered thiazole orange moiety is able to intercalate and subseq
25                            The intercalator (thiazole orange or benzothiazole orange) provides an anc
26  studies have observed a correlation between thiazole orange-positive platelets and platelet synthesi
27                                  The EC50 of thiazole orange-positive platelets from IL-6-treated dog
28               Because it has been shown that thiazole orange specifically labels a subpopulation of d
29 ls were determined using flow cytometry with thiazole orange staining.
30 s on markers of platelet age have focused on thiazole orange-staining for enumeration of "reticulated
31 ome conjugates also include a fluorescein or thiazole orange tag.
32 ncentrations when aromatic molecules such as thiazole orange template the quadruplex formation.
33 a series of fluorinated analogues of the dye thiazole orange that exhibit improved fluorescence quant
34 o acids, heptaethylene glycol, spermine, and thiazole orange through CuAAC click chemistry.
35                                              Thiazole orange (TO) derivatives are fluorescent interca
36 which two (or more) intercalator dyes of the thiazole orange (TO) family serve as nucleobase surrogat
37                              The cyanine dye thiazole orange (TO) is a well-known fluorogenic stain f
38 ntally sensitive dyes Thioflavin T (ThT) and Thiazole Orange (TO) is strongly dependent on the type o
39 ated and the anionic hydrogel binds cationic thiazole orange (TO), signaled by enhanced fluorescence.
40 the erstwhile used structurally related dye, Thiazole Orange (TO), which did not induce any quadruple
41 PNA analogues having intrinsic fluorescence, thiazole orange (TO)-PNA and [bis-o-(aminoethoxy)phenyl]
42 e efficient binding of the intercalating dye thiazole orange (TO).
43 mer, bis-benzimide (DAPI), Hoechst 33258 and thiazole orange] to function as suitable reporter molecu
44 rs at 60 degrees , akin to the classical FMR thiazole orange (TO1).
45 des/assay with ethiduim bromide or less with thiazole orange), with a rapid readout using a fluoresce