ライフサイエンスコーパス: cRNA probe

1 bridization with digoxigenin-labeled pro-TRH cRNA probe.

2 y with a digoxigenin (DIG)-labeled antisense cRNA probe.

3 a chromosome 17 library with a specific K13 cRNA probe.

4 ng in situ hybridization with an 35S-labeled cRNA probe.

5 ains were sectioned and hybridized with a PR cRNA probe.

6 histochemistry (ISHH) with a novel sensitive cRNA probe.

7 idization histochemistry (ISHH) with a novel cRNA probe.

8 analyzed by using in situ hybridization with cRNA probes.

9 u hybridization using specific (35)S-labeled cRNA probes.

10 ization histochemistry using monkey-specific cRNA probes.

11 in situ hybridization, using monkey-specific cRNA probes.

12 situ hybridization using digoxigenin-labeled cRNA probes and an alkaline phosphatase-conjugated anti-

13 n situ hybridization histochemistry, using a cRNA probe coding for the NMDAR1 receptor subunit, revea

14 experiments, using two independent rat CFTR cRNA probes, expression of CFTR could not be detected in

15 ed with radiolabeled and digoxygenin-labeled cRNA probes for alpha-synuclein, parkin, and UCH-L1 mRNA

16 with nonisotopic in situ hybridization with cRNA probes for glutamic acid decarboxylase 65 (GAD65) a

17 situ hybridization was used with 35S-labeled cRNA probes for the different ionotropic receptor subuni

18 u hybridization, using 35S-labeled antisense cRNA probes for the V2 receptor demonstrated strong labe

19 he present study we used digoxigenin-labeled cRNA probes for the vesicular glutamate transporters, VG

20 Hybridization of cRNA probes for trkB or trkC showed a time-dependent red

21 To this end, we generated biotinylated cRNA probes from livers of age-matched infants with the

22 using in situ hybridization and a 249 bp TPH cRNA probe generated with RT-PCR (n = 5 animals/group).

23 the authors used in situ hybridization with cRNA probes generated from cDNA for rod opsin and red, g

24 A cRNA probe identifying both mRNAs showed that the transc

25 ined using a digoxigenin-labeled DNPI/VGLUT2 cRNA probe in the present study to determine which, if a

26 IRP binding is abrogated when APP cRNA probe is mutated in the core IRE domain (Delta4 bas

27 ybridization was performed using full-length cRNA probes labeled with 35S-UTP.

28 idization was performed by using full-length cRNA probes labeled with 35S-UTP.

29 Amplified cRNA probes mixed with a universal standard were hybridi

30 In situ hybridization using an R-Ras3 cRNA probe revealed high levels of R-Ras3 transcripts in

31 In situ hybridization using cRNA probes revealed that these beta-subunit genes are h

32 ervous system tissue utilizing ceruloplasmin cRNA probes reveals abundant ceruloplasmin gene expressi

33 situ hybridization with isotopically labeled cRNA probes showed that trkB and trkC mRNAs were express

34 ng in situ hybridization with [33P] labelled cRNA probe specific for the long form of the receptor mR

35 nkey thalamus by in situ hybridization using cRNA probes specific for alpha 1, alpha 2, alpha 3, alph

36 Using antibodies and cRNA probes specific for alpha1A channels, we found that

37 In situ hybridization with cRNA probes specific for the 1B transcript showed the me

38 yes were cut and hybridized with 35S-labeled cRNA probes specific for the glucocorticoid receptor, mi

39 rvical spinal cords by using ISHH with novel cRNA probes specific for the mRNA encoding functional GH

40 ly specific affinity-purified antibody and a cRNA probe to generate a detailed mapping of BDNF immuno

41 ith in situ hybridization techniques using a cRNA probe to the exon encoding mature rat BDNF protein.

42 echnique using digoxigenin and (35)S-labeled cRNA probes to analyze, in detail, the expression of ER

43 sing digoxigenin-labeled antisense and sense cRNA probes to human APOE.

44 u hybridization histochemistry (ISHH), using cRNA probes to NMDAR1.

45 ved upon hybridization of radiolabeled (35S) cRNA probes to thin sections of reproductive tissues (ma

46 is method was performed using a 35S-labelled cRNA probe, transcribed in vitro from the rat ovarian ar

47 tions hybridized with sense p55 and p75 TNFR cRNA probes was comparable to background.

48 ybridization histochemistry with radioactive cRNA probes was used to study patterns of gene expressio

49 clease protection assay and species-specific cRNA probes, we measured mRNA expression levels of andro

50 Digoxigenin-labeled cRNA probes were prepared by run-off transcription from

51 Radiolabeled human cRNA probes were used to map the distribution of the two

52 Radioactive complementary RNA (cRNA) probes were prepared from cDNAs specific for alpha