ライフサイエンスコーパス: nonisotopic

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1 Using new nonisotopic and isotopic methods, we showed previously t

2 c clumps is the basis of a rapid and simple, nonisotopic assay for nucleoid denaturation.

3 We describe a homogeneous and nonisotopic assay for PI 4-kinase activity based on the

4 Using a nonisotopic cellfree physical binding assay, those Fc ch

5 standard NCFBAs by developing a quantitative nonisotopic chemiluminescent method using biotin-labeled

6 IP-RP-HPLC) procedure has been developed for nonisotopic detection of isoaspartic acid residues in pr

7 Combined isotopic/nonisotopic double-labeling in situ hybridization demons

8 We present here a fast, nonisotopic, fluorescence-based assay for the detection

9 We report a sensitive, nonisotopic, fluorescence-based method for the detection

10 A nonisotopic heteroduplex complexity assay (HCA) was firs

11 pha 2 receptor class, were examined by using nonisotopic in situ hybridization and immunohistochemist

12 y obstruction (EBO), and normal liver, using nonisotopic in situ hybridization and immunohistochemist

13 By using a highly sensitive nonisotopic in situ hybridization method and immunostain

14 ound gold after injections into the VTA with nonisotopic in situ hybridization of the vesicular gluta

15 with a monoclonal antibody to GABA and with nonisotopic in situ hybridization with cRNA probes for g

16 Using nonisotopic in situ hybridization, we demonstrate GLAST

17 medullary CA nuclei using combined isotopic/nonisotopic in situ hybridization.

18 ng (AR), isografted, and naive animals using nonisotopic in situ hybridization.

19 The use of this sensitive nonisotopic ISH method should allow detection of other K

20 ad transition from radioisotopic labeling to nonisotopic labeling over the last two decades.

21 ay, indicating that biotinylation provides a nonisotopic labeling strategy for large-scale screens.

22 In a blind field evaluation of a nonisotopic liquid hybridization assay for detection of

23 The polymerase chain-reaction-based nonisotopic liquid hybridization assay was better than c

24 d use of isotopic quantitation reference and nonisotopic mass coding of samples.

25 findings document the utility of RDE for the nonisotopic measurement of neurotransmitter influx and e

26 which provides an ultraefficient, fast, and nonisotopic method for the detection of protein-RNA inte

27 using identical solution conditions and the nonisotopic method that we have developed.

28 Additionally, nonisotopic methods for quantitating platelet survival h

29 ative agreement between the isotopic and the nonisotopic methods.

30 In this study, a novel nonisotopic nucleic acid ISH method using catalyzed sign

31 ese techniques still catalyze the search for nonisotopic procedures to estimate platelet survival as

32 ation of the chemical structure diversity of nonisotopic reagents to significantly enhance the MS det

33 Screening of nonisotopic reagents used combinatorial libraries of pep

34 he proband and her affected brother, using a nonisotopic RNase cleavage assay, revealed the partial s

35 human oral keratinocytes were examined by a nonisotopic RNase cleavage assay.

36 We have developed a nonisotopic RNase protection assay using RNA probes that

37 cal method is somewhat limited by the use of nonisotopic spikes, the sensitivity allows for the deter

38 ssay over other kinase assays include use of nonisotopic substrates and a more simple procedure in wh

39 It has the added advantage of using nonisotopic substrates.

40 icating the high feasibility of (242)Pu as a nonisotopic tracer for (237)Np determination in real uri

41 (242)Pu was utilized as a nonisotopic tracer to monitor the chemical yield of (237

42 The use of nonisotopic tracers was investigated in order to allow f

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