ライフサイエンスコーパス: immuno-electron microscopy

1 nassociated with coated pits, as assessed by immuno-electron microscopy.

2 d all three motor proteins, as determined by immuno-electron microscopy.

3 py and stained isolated flagellar ribbons by immuno-electron microscopy.

4 of the yeast alpha-factor receptor Ste2p by immuno-electron microscopy.

5 immunofluorescence, protease protection and immuno-electron microscopy.

6 radiatum of adult rat hippocampus, by using immuno-electron microscopy after chemical fixation.

7 Using live cell imaging and immuno-electron microscopy analyses of tobacco epidermal

8 ikingly, ultrastructural analyses, including immuno-electron microscopy and electron microscopic tomo

9 Here we use immuno-electron microscopy and electron tomography to sh

10 ultrastructural distribution by quantitative immuno-electron microscopy and its biochemical interacti

11 Immuno-electron microscopy and quantitative spatial mapp

12 Immuno-electron microscopy and super-resolution imaging

13 Using immuno-electron microscopy as well as a recently develop

14 Immuno-electron microscopy confirmed the presence of gK

15 Immuno-electron microscopy demonstrated that MAb 8E7 rea

16 mitochondrial fractions in combination with immuno-electron microscopy demonstrates that Arg II is c

17 Immuno-electron microscopy demonstrates that these spots

18 Immuno-electron microscopy demonstrates that Vilya is a

19 eltavph1 mutant as shown by Western blot and immuno-electron microscopy, despite a complete lack of l

20 Western blots and immuno-electron microscopy detected a few copies of gp13

21 We used immuno-electron microscopy (EM) to locate KAHRP in these

22 Together with immuno-electron microscopy experiments that indicated AC

23 In immuno-electron microscopy experiments these compartment

24 ved megakaryocytes (MKs) by conventional and immuno-electron microscopy from Vps33b(fl/fl)-ER(T2) mic

25 Immunofluorescence and immuno-electron microscopy have been used to test the hy

26 Localization by immuno-electron microscopy illustrates a unique pattern

27 e serotonergic cells may exert, we have used immuno-electron microscopy in this study to examine the

28 tein distribution (by immunofluorescence and immuno-electron microscopy), including codistribution wi

29 in possesses four transmembrane domains, and immuno-electron microscopy localizes the endogenous prot

30 With immuno-electron microscopy methods, these capsids were s

31 escence histochemistry, confocal microscopy, immuno-electron microscopy, molecular biology, and cell

32 Double-label immuno-electron microscopy of hypothalamic sections labe

33 Immuno-electron microscopy of infected cells indicated t

34 Immuno-electron microscopy of leaf tissue and western an

35 Immunofluorescence and immuno-electron microscopy reveal that ODA10 in flagella

36 Immunofluorescence and immuno-electron microscopy revealed LmAQP1 to be localiz

37 ytes maintained an active TCA cycle, whereas immuno-electron microscopy revealed that fine astrocytic

38 In addition, immuno-electron microscopy revealed that tau-positive fi

39 Immuno-electron microscopy reveals that the latter are d

40 Immuno-electron microscopy showed that OGT is localized

41 Immuno-electron microscopy showed that Rab27b was associ

42 oducing cells organized into islet clusters; immuno-electron microscopy showed typical insulin-contai

43 Furthermore, immuno-electron microscopy studies confirm that IRS-1 an

44 in localizing specific cellular proteins by immuno-electron microscopy techniques limits application

45 Here, we show by immuno-electron microscopy that AP-3 is associated with

46 dy was to determine by means of quantitative immuno-electron microscopy the expression of PGC-1alpha

47 The goal of the present study is to use Iba1 immuno-electron microscopy to elucidate the fine structu

48 Here, we used quantitative immuno-electron microscopy to examine the possibility th

49 We employed immuno-electron microscopy to investigate the ultrastruc

50 Thus, in this study, dual immuno-electron microscopy was performed to determine wh

51 Immuno-electron microscopy was performed using mouse car

52 Using pre-embedding immuno-electron microscopy, we found human synaptophysin

53 born neurons of the mouse dentate gyrus with immuno-electron microscopy, we found output synapses tha

54 pecific ablation, whole cell patch-clamp and immuno-electron microscopy, we found that NAc inputs syn

55 Using immuno-electron microscopy, we observed Ab deposits equa

56 protein immunoreactive inclusions, which by immuno-electron microscopy were confined to paired helic