1 ltaneously to characterize these vesicles by
immunolabelling.
2 eptide- and nicotinic acetylcholine receptor-
immunolabelling.
3 Immunolabelling analysis and ultrastructural observation
4 peptidase in Escherichia coli, was mapped by
immunolabelling and by visualization of GFP fusion prote
5 opment we combined fate-mapping of ENCC with
immunolabelling and intravascular dye injection to visua
6 We used a combination of
immunolabelling and RNA/DNA fluorescence in situ hybridi
7 In all these areas,
immunolabelling appeared specific since it was abolished
8 s) rats by immunoblotting and post-embedding
immunolabelling at electron microscope level.
9 SUMO1 knock-out mice showed that anti-SUMO1
immunolabelling at synapses is non-specific.
10 he neuropil of hippocampus, with patterns of
immunolabelling characteristic enough to suggest the dia
11 By contrast,
immunolabelling data have shown that Purkinje cells from
12 Immunolabelling demonstrated a high density of PDGFRalph
13 Immunolabelling demonstrated TMC1 throughout the stereoc
14 Myelin basic protein and neurofilament
immunolabelling demonstrates that axons in these adjacen
15 ell function and neoplasia we have performed
immunolabelling experiments to determine their subcellul
16 Double-
immunolabelling for poly(ADP-ribose) and markers of neur
17 Double
immunolabelling for poly(ADP-ribose) and microtubule-ass
18 Double-
immunolabelling for poly(ADP-ribose) and tau or A beta-p
19 By
immunolabelling in mouse testes we show that TGIF is exp
20 Immunolabelling localised DRP2A/B to the tips of root ha
21 Post-embedding
immunolabelling methods were applied to semi-thin and ul
22 Immunolabelling of 12 weeks old skin specimens showed st
23 Her skeletal muscle biopsy showed reduced
immunolabelling of alpha-dystroglycan.
24 ction in hexaploid wheat (2n = 42) by triple
immunolabelling of CENH3 protein marking functional cent
25 co-expression with DsRed fusions along with
immunolabelling of stably transformed BY2 cells indicate
26 We optimize
immunolabelling of tail epidermal wholemounts to allow s
27 In each patient,
immunolabelling of the neuromuscular junction for rapsyn
28 In aged rats,
immunolabelling patterns and the density of immunogold p
29 we show that by using specific intracellular
immunolabelling protocols, FACS separation of interphase
30 ia expressed intimin, and of those that did,
immunolabelling revealed a uniform distribution of intim
31 Double
immunolabelling revealed numerous GLP-1-IR nerve fibers
32 Immunolabelling revealed reduced density of sensory (CGR
33 Critically,
immunolabelling shows the dynamics of these presynaptic
34 Immunolabelling studies demonstrated that the immediate
35 Immunolabelling studies revealed qualitatively normal di
36 In double-
immunolabelling studies, histamine fibres were found in
37 tor (M(3)AChR) and lysosomes was examined by
immunolabelling techniques.
38 brain changes or abnormal alpha-dystroglycan
immunolabelling,
unlinked to any reported CMD loci.
39 Immunolabelling was also evident beneath the plasma memb
40 prelimbic cortex (area 32), a gradient of CN
immunolabelling was found in the somata and processes of
41 GluA2
immunolabelling was stronger in MCs than in BCs.
42 Intercalated disk morphology and connexin 43
immunolabelling were not different in hypertrophy.
43 Highest levels of
immunolabelling were observed in the anterior, amygdalo-
44 ese terminals to Renshaw cells, we used dual
immunolabelling with antibodies against gephyrin or calb
45 Immunolabelling with antibodies against Sm proteins show
46 Double
immunolabelling with CRH antiserum revealed that CART in
47 Retrograde labelling and dual
immunolabelling with nNOS revealed that those AT1R-immun
48 eport on the expression of this new protein:
immunolabelling with the antibody (designated NCL-hamlet