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1 Untagged, recombinant C2A was double-labeled with 13C and 15N, and triple-resonance NM

2 Furthermore, pyknotic O4+ OLs were double-labeled with 4-HNE.

3 test this hypothesis, sartorius muscles were double labeled with a fluorescent dye, 4-(4-diethylamino

4 Agarose-embedded sections were double labeled with a panel of antibodies.

5 eled cells at the hilar/CA3 border also were double-labeled with a neuronal marker (NeuN).

6 ot in the MICG, and some of these cells were double labeled with an antiserum to the glial protein S-

7 emistry of the skin showed CD1a-positive DCs double-labeled with an antibody against DV envelope glyc

8 , ii) single-stained with anti-APP, and iii) double-labeled with anti-APP and AT8.

9 veola-sized vesicular profiles that could be double-labeled with anti-dystrophin and anti-cav-3 antib

10 readily identified in the aorta and could be double labeled with antibodies to CD11c and antigen-pres

11 cal glia/fibroblasts in primary culture were double labeled with antibodies to glial fibrillary acidi

12 rgic nature of the TH-i cells, sections were double-labeled with antibodies to dopamine transporter (

13 When mouse retina were double labeled with B16 and anti-alpha-actinin, B16 was

14 rols (n=5), c-Fos-positive cells and neurons double-labeled with c-Fos and beta-endorphin, enkephalin

15 Moreover, neurons double-labeled with c-Fos and choline acetyltransferase

16 on (n=5), c-Fos immunoreactivity and neurons double-labeled with c-Fos and either enkephalin or 5-HT

17 Moreover, neurons double-labeled with c-Fos and enkephalin in the rVLM wer

18 More neurons double-labeled with c-Fos and nitric oxide synthase (NOS

19 ulation), c-Fos immunoreactivity and neurons double-labeled with c-Fos, an immediate early gene and t

20 ocessed, and frozen; 80-nm cryosections were double labeled with combinations of CCR5, CXCR4, and CD4

21 demonstrated that nearly all TH-i cells were double-labeled with DAT, suggesting that they contain th

22 P2X5 receptors double labeled with differentiated fetal keratinocytes t

23 The retinas were double labeled with either anti-vimentin and anti-long/m

24 clei, hypothalamic, and forebrain areas were double labeled with FG and Fos, the results suggest that

25 % of the remaining Rbpms-positive cells were double-labeled with FG.

26 -HT-immunoreactive (5-HT-ir) cells were also double-labeled with FG.

27 Brains were double labeled with fluorescence in situ hybridization o

28 The IL1beta-IR cells double-labeled with glial fibrillary acidic protein (GFA

29 ically characterized auditory neurons can be double-labeled with HRP and Fos after iontophoretic inje

30 pale and thick stripes; 10-27% of cells were double labeled, with most located in interpatches.

31 The percentage of GnRH neurons that double-labeled with NMDA-R1 was 2% in prepubertal rats a

32 tures that in the human VZ/SVZ, cells can be double labeled with RG markers and calretinin (CalR) and

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