ライフサイエンスコーパス: TIRFM

1 TIRFM also increased in response to Gd3+, a competitive

2 TIRFM and biotinylation assays show robust receptor- and

3 TIRFM data were confirmed in human DAT-N2A cells using b

4 TIRFM images were acquired by a cooled CCD camera in app

5 We did, however, observe a TIRFM response to epidermal growth factor (EGF).

6 his study, we report the implementation of a TIRFM-based polarization technique to detect rapid submi

7 Single-cell capacitance and TIRFM measurements of exocytosis revealed a selective su

8 Variable-angle TIRFM experiments were conducted to calibrate the coupli

9 ructed for computer-automated multiple angle-TIRFM (MA-TIRFM) using a right angle F2 glass prism (n(r

10 Furthermore, two-color TIRFM showed that Rab11a-mCherry was present in rhodopsi

11 resonance (SPR) angle for gold film enhanced TIRFM.

12 scope, the stage of which was configured for TIRFM imaging of fluorescently labeled human umbilical v

13 parameter, are automatically estimated from TIRFM image sequences, to account for both the lateral d

14 Furthermore, TIRFM showed that H(2)O(2) triggered membrane traffickin

15 We observed no increase in TRPC3-GFP TIRFM in response to the muscarinic receptor agonist met

16 sicle fusion event at the plasma membrane in TIRFM image sequences.

17 Live observation of fibrin polymerization in TIRFM by diffusive mixing of thrombin and plasma reveale

18 ocus drift compensation, a common problem in TIRFM due to the narrow excitation depth, particularly w

19 aser light, the typical excitation source in TIRFM, often creates spatial interference fringes across

20 MA-TIRFM was used to compare with nanometer z-resolution th

21 These studies establish MA-TIRFM for measurement of submicroscopic distances betwee

22 ica lens (458 mm radius, n(r) 1.463); the MA-TIRFM map accurately reproduced the lens spherical surfa

23 computer-automated multiple angle-TIRFM (MA-TIRFM) using a right angle F2 glass prism (n(r) 1.632) t

24 internal reflection fluorescence microscope (TIRFM) was constructed and tested for the highest vertic

25 internal reflection fluorescence microscope (TIRFM) was used for optical imaging of exocytosis and su

26 internal reflection fluorescence microscopy (TIRFM) achieves subdiffraction axial sectioning by confi

27 internal reflection fluorescence microscopy (TIRFM) and kinetic and thermodynamic measurements, we es

28 internal reflection fluorescence microscopy (TIRFM) and wide-field imaging of live cells to analyze t

29 internal reflection fluorescence microscopy (TIRFM) for high resolution imaging and molecular transpo

30 internal reflection fluorescence microscopy (TIRFM) from the apical side, allowed us to visualize the

31 internal reflection fluorescence microscopy (TIRFM) has joined confocal microscopy as a complementary

32 internal reflection fluorescence microscopy (TIRFM) images obtained at multiple incident angles.

33 internal reflection fluorescence microscopy (TIRFM) images the plasma membrane-cytosol interface and

34 internal reflection fluorescence microscopy (TIRFM) is becoming an increasingly common methodology to

35 nternal reflectance fluorescence microscopy (TIRFM) is reported that allows quantification of the pen

36 internal reflection fluorescence microscopy (TIRFM) is the method of choice to visualize a variety of

37 internal reflection fluorescence microscopy (TIRFM) is well suited to focus on the late steps of exoc

38 internal reflection fluorescence microscopy (TIRFM) studies suggest that some LDCVs, although being a

39 internal reflection fluorescence microscopy (TIRFM) to examine the transmission of force from the api

40 internal reflection fluorescence microscopy (TIRFM) to investigate the characteristics of the yeast h

41 internal reflection fluorescence microscopy (TIRFM) to visualize the spatial-temporal recruitment of

42 internal reflection fluorescence microscopy (TIRFM) to visualize vesicular fusion events in astrocyte

43 internal reflection fluorescence microscopy (TIRFM), combined with single particle tracking, to probe

44 internal reflection fluorescence microscopy (TIRFM), custom software-based detection, and selective p

45 internal reflection fluorescence microscopy (TIRFM), the dynamics of bovine serum albumin (BSA) and h

46 internal reflection fluorescence microscopy (TIRFM), these "molecular curtains" allow for the direct

47 internal reflection fluorescence microscopy (TIRFM), we monitored green fluorescent protein-labeled T

48 internal reflection fluorescence microscopy (TIRFM)-based assay.

49 internal reflection fluorescence microscopy (TIRFM).

50 internal reflection fluorescence microscopy (TIRFM).

51 internal reflection fluorescence microscopy (TIRFM).

52 internal reflection fluorescence microscopy (TIRFM).

53 internal reflection fluorescence microscopy (TIRFM).

54 internal reflection fluorescence microscopy (TIRFM).

55 internal reflection fluorescent microscopy (TIRFM) to image DRD2 with a superecliptic pHluorin tagge

56 is study shows that in vitro single-molecule TIRFM provides a new window into the molecular mechanism

57 The unique illumination geometry of TIRFM also enables a distinct method to create an excita

58 ine adrenal chromaffin cells using polarized TIRFM demonstrate rapid and varied submicrometer changes

59 e find that azimuthal beam spinning produces TIRFM images that more accurately portray the real fluor

60 The application of our method on 16 real TIRFM image sequences additionally revealed differences

61 ioning effect, reduces contrast, and renders TIRFM-image quantification uncertain.

62 ernal reflection fluorescence microscope (SA-TIRFM).

63 internalize particular GPCRs, we adapted the TIRFM imaging assay to simultaneously quantify the inter

64 to minimize these fringes by modulating the TIRFM field during a frame capture period; however, thes

65 Third, TIRFM enables direct observation of rare events in which

66 This TIRFM response to EGF was accompanied by increased Ba2+

67 Data presented here from real-time TIRF (TIRFM) and confocal microscopy coupled with surface biot

68 Here we present an alternative to TIRFM, termed variable-angle epifluorescence microscopy

69 Particularly in objective-type TIRFM, large deviations from the exponential intensity d

70 Here, using VA-TIRFM and FLIM-FRET, we revealed that AtHIR1 is present

71 measurement and visualization of LDCVs with TIRFM.