1 cellular NanoBRET-based binding studies in a
nonisotopic and high-throughput manner.
2 Using new
nonisotopic and isotopic methods, we showed previously t
3 c clumps is the basis of a rapid and simple,
nonisotopic assay for nucleoid denaturation.
4 We describe a homogeneous and
nonisotopic assay for PI 4-kinase activity based on the
5 Using a
nonisotopic cellfree physical binding assay, those Fc ch
6 standard NCFBAs by developing a quantitative
nonisotopic chemiluminescent method using biotin-labeled
7 IP-RP-HPLC) procedure has been developed for
nonisotopic detection of isoaspartic acid residues in pr
8 Combined isotopic/
nonisotopic double-labeling in situ hybridization demons
9 We present here a fast,
nonisotopic,
fluorescence-based assay for the detection
10 We report a sensitive,
nonisotopic,
fluorescence-based method for the detection
11 A
nonisotopic heteroduplex complexity assay (HCA) was firs
12 pha 2 receptor class, were examined by using
nonisotopic in situ hybridization and immunohistochemist
13 y obstruction (EBO), and normal liver, using
nonisotopic in situ hybridization and immunohistochemist
14 By using a highly sensitive
nonisotopic in situ hybridization method and immunostain
15 ound gold after injections into the VTA with
nonisotopic in situ hybridization of the vesicular gluta
16 with a monoclonal antibody to GABA and with
nonisotopic in situ hybridization with cRNA probes for g
17 Using
nonisotopic in situ hybridization, we demonstrate GLAST
18 medullary CA nuclei using combined isotopic/
nonisotopic in situ hybridization.
19 ng (AR), isografted, and naive animals using
nonisotopic in situ hybridization.
20 The use of this sensitive
nonisotopic ISH method should allow detection of other K
21 ad transition from radioisotopic labeling to
nonisotopic labeling over the last two decades.
22 ay, indicating that biotinylation provides a
nonisotopic labeling strategy for large-scale screens.
23 In a blind field evaluation of a
nonisotopic liquid hybridization assay for detection of
24 The polymerase chain-reaction-based
nonisotopic liquid hybridization assay was better than c
25 d use of isotopic quantitation reference and
nonisotopic mass coding of samples.
26 findings document the utility of RDE for the
nonisotopic measurement of neurotransmitter influx and e
27 which provides an ultraefficient, fast, and
nonisotopic method for the detection of protein-RNA inte
28 using identical solution conditions and the
nonisotopic method that we have developed.
29 Additionally,
nonisotopic methods for quantitating platelet survival h
30 ative agreement between the isotopic and the
nonisotopic methods.
31 In this study, a novel
nonisotopic nucleic acid ISH method using catalyzed sign
32 ese techniques still catalyze the search for
nonisotopic procedures to estimate platelet survival as
33 ation of the chemical structure diversity of
nonisotopic reagents to significantly enhance the MS det
34 Screening of
nonisotopic reagents used combinatorial libraries of pep
35 he proband and her affected brother, using a
nonisotopic RNase cleavage assay, revealed the partial s
36 human oral keratinocytes were examined by a
nonisotopic RNase cleavage assay.
37 We have developed a
nonisotopic RNase protection assay using RNA probes that
38 cal method is somewhat limited by the use of
nonisotopic spikes, the sensitivity allows for the deter
39 ssay over other kinase assays include use of
nonisotopic substrates and a more simple procedure in wh
40 It has the added advantage of using
nonisotopic substrates.
41 icating the high feasibility of (242)Pu as a
nonisotopic tracer for (237)Np determination in real uri
42 (242)Pu was utilized as a
nonisotopic tracer to monitor the chemical yield of (237
43 The use of
nonisotopic tracers was investigated in order to allow f