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 split-GFP experiments loc

13 Immuno-electron microscopy and super-resolution imaging

14 we used structured illumination microscopy, immuno-electron microscopy, and mass spectrometry to est

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

16 Immuno-electron microscopy confirmed the presence of gK

17 Immunofluorescence and immuno-electron microscopy demonstrated strong targeting

18 Immuno-electron microscopy demonstrated that MAb 8E7 rea

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

20 Immuno-electron microscopy demonstrates that these spots

21 Immuno-electron microscopy demonstrates that Vilya is a

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

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

24 Immuno-electron microscopy (EM) of synaptosomes uncovere

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

26 Together with immuno-electron microscopy experiments that indicated AC

27 In immuno-electron microscopy experiments these compartment

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

29 Immuno-electron microscopy further revealed that V-type

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

31 r, here identified as collagen VI (COLVI) by immuno-electron microscopy (IEM) and mass-spectrometry.

32 Localization by immuno-electron microscopy illustrates a unique pattern

33 h electron cryo-tomography and complementary immuno-electron microscopy in mammalian cell lines.

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

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

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

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

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

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

40 Immuno-electron microscopy of infected cells indicated t

41 Immuno-electron microscopy of leaf tissue and western an

42 Immuno-electron microscopy of mouse atria showed MyBP-HL

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

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

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

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

47 Immuno-electron microscopy reveals that the latter are d

48 Immuno-electron microscopy showed that OGT is localized

49 Immuno-electron microscopy showed that Rab27b was associ

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

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

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

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

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

55 Here, we used cryo- and immuno- electron microscopy to characterise filaments th

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

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

58 We employed immuno-electron microscopy to investigate the ultrastruc

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

60 Immuno-electron microscopy was performed using mouse car

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

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

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

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

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