ライフサイエンスコーパス: by immunolabeling

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1 Protein localization was ascertained by immunolabeling.

2 nd Cx30 in the saccule, utricle, and ampulla by immunolabeling.

3 on, and tissue distribution were established by immunolabeling.

4 l T lymphocytes, but not smooth muscle cells by immunolabeling.

5 The mCherry distribution was evaluated by immunolabeling.

6 virally transfected fluorescent labeling or by immunolabeling after fixation.

7 sitions of several SAGA subunits were mapped by immunolabeling and by analysis of mutant complexes.

8 Analysis of cellular location by immunolabeling and fluorescence microscopy suggests t

9 nner, and its identity as Ara h 1 was proven by immunolabeling and mass spectrometry.

10 TRPV4 protein expression was measured by immunolabeling and Western blotting.

11 the absence of loricrin, which was confirmed by immunolabeling, and the absence of the distinctive lo

12 Their bipolar cell input was studied by immunolabeling experiments using various bipolar cell

13 rted by relative cell size and characterized by immunolabeling for beta1 integrin, nuclear transcript

14 rdiac progenitor cell population as assessed by immunolabeling for c-kit in combination with myocyte-

15 the islet-exocrine interface was identified by immunolabeling for collagen I, IV, V or VI and islets

16 ounts for phase-contrast microscopy followed by immunolabeling for fluorescence microscopy and embedd

17 r macula, and posterior crista, as confirmed by immunolabeling for hair cell antigen (HCA) by stage 2

18 islets identified either morphologically or by immunolabeling for insulin.

19 (n = 98) and astrocytes (n = 10), as well as by immunolabeling for specific connexins, the molecular

20 Molecules that were identified by immunolabeling in NS cells included nestin, Chx-10, v

21 tion intermediates that are readily detected by immunolabeling methods.

22 and analyzed their behavior at the membrane by immunolabeling protocols, fluorescence recovery after

23 ons, allowed us to identify distinct neurons by immunolabeling small subsets of sections within large

24 the hair cell lateral membrane was confirmed by immunolabeling studies.

25 his process, we attempted to locate synapses by immunolabeling taste buds of rats for proteins involv

26 ber proteins (MFPs) 1 and 2 and demonstrated by immunolabeling that both are located in the MSP cytos

27 networks in their cytoplasm, and demonstrate by immunolabeling that these networks contain Ure2p.

28 proteoglycans (CSPGs), which were identified by immunolabeling; this association is maintained in the

29 BetaCTFs were co-localized by immunolabeling to vesicular compartments, including t

30 pendent changes in ribosomes were visualized by immunolabeling using an antibody, called Y10B, that r

31 the cellular distribution of CRF in the VTA by immunolabeling VTA sections with anti-CRF antibodies

32 and regeneration of efferent nerve terminals by immunolabeling whole-mount cochleae for differentiall

33 Sections of rat medulla were examined by immunolabeling with a polyclonal antibody directed ag

34 tinal blood vessel formation was quantitated by immunolabeling with an anti-type-IV collagen antibody

35 s were further characterized at 37 degrees C by immunolabeling with specific antibodies recognizing o

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