ライフサイエンスコーパス: double staining

1 lymphocytes were proliferating (assessed by double staining).

2 sed in flow cytometry and immunofluorescence double staining.

3 l apoptosis was assessed by MUC5AC and TUNEL double staining.

4 Apoptosis was quantified using double staining.

5 Finally, double-staining analyses showed that the majority of p53

6 Double staining and confocal microscopic analysis reveal

7 ta of ERG and IL-6 using immunohistochemical double staining and correlated the read-out with clinico

8 In a double staining approach, we simultaneously measured OSN

9 Double staining confirmed that both the conformation-spe

10 Immunohistochemistry and double staining confirmed the expression of FcRn recepto

11 Immunofluorescence double staining demonstrates that the Na(+)-K(+)-Cl(-) c

12 Immuno-double-staining experiments in Saccharomyces cerevisiae

13 Histochemical analysis (double staining for alkaline phosphatase and dipeptidyl

14 Double staining for cardiomyocytes with alpha sarcomeric

15 Double staining for CAS and Ki-67 revealed co-expression

16 Double staining for Dmp1 and Ki67 revealed that these tw

17 s confirmed by using confocal microscopy and double staining for glial fibrillary acidic protein (GFA

18 Double staining for host macrophages and SPIO particles

19 Double staining for Luxol fast blue and Bielshowsky was

20 Double staining for oxytocin or vasopressin neurons reve

21 pression in synaptic terminals was tested by double staining for palladin and gamma-aminobutyric acid

22 characteristically is punctate, we performed double staining for palladin and the presynaptic marker

23 irect evidence for apoptosis was obtained by double staining for terminal deoxynucleotide transferase

24 ting capability of Combo NP was evaluated by double staining for TUNEL and alpha-SMA at various time

25 Double-staining for CD83 and CD4 revealed that mDCs asso

26 ormation of daughter cells was visible after double-staining for Ki67 and ZO-1.

27 excised, and immunofluorescence single- and double-staining for multiple markers was performed for e

28 e renal sympathetic pathways were located by double-staining for the neuronal isoform of nitric oxide

29 We used double staining histochemistry to investigate the relati

30 Double staining IHC showed that axonal terminals of both

31 Double staining immunoassays that used anti-MERS-CoV ant

32 rons in the area of the AH are identified by double-staining immunocytochemistry and laser scanning c

33 Double staining immunofluorescence was used to label uPA

34 By double staining immunofluorescence we showed that IL-6 i

35 Double-staining immunofluorescence studies showed coloca

36 intracellular localization of ICP0, we used double-staining immunofluorescence tests to examine the

37 Double staining immunohistochemistry was also used to in

38 Double staining immunohistochemistry was employed to eva

39 Double-staining immunohistochemistry showed CXCL9 co-loc

40 le blood and lesional morphea skin, and used double-staining immunohistochemistry to determine the cu

41 The double staining in the flatmounted retinas demonstrated

42 idian Otx (Hroth) and a Hox gene (HrHox1) by double-staining in situ hybridizations indicate that the

43 TUNEL), hematoxylin, and immunohistochemical double staining methods.

44 y bromodeoxyuridine (BrdU) incorporation and double staining of BrdU with nestin, Tuj1, or the neuron

45 ophages were evaluated by immunofluorescence double staining of CD68 and H1R on human skin sections.

46 colocalized with ganglioside GM1 as seen by double staining of fixed cells.

47 Double staining of insulin and non-beta cell hormones in

48 abeled cones in the retina were confirmed by double staining of mouse retina sections with the anti-R

49 Double staining of native eve protein and transgene mRNA

50 CD71/RNA double staining of reticulocytes enriched from adult per

51 Double staining of transgenic mouse brain sections with

52 y fundus fluorescein angiography, histology, double-staining of FITC-dextran perfusion and elastin im

53 Double-staining of neurons in the PVN for AVP and OT sho

54 artifacts and interferences, and developed a double-staining procedure that allows visualization and

55 Using double-staining protocols, we detected activated NF-kapp

56 Double staining revealed that these cells were distinct

57 BrdU-beta-galactosidase double-staining revealed an inverse correlation between

58 Double staining showed co-localization of Gal-3 with OX-

59 ted from the leading half of the cell, where double staining showed myosin II was present.

60 Double staining showed that activated macrophages/microg

61 In situ hybridization and immunochemistry double staining showed that miR-365 was expressed in neu

62 Immunohistochemistry double staining showed that proteasome 20S-alpha4 and -a

63 Double staining showed that suppression of c-fos express

64 ile n847 immunofluorescence and Thioflavin-S double-staining showed that a subset of n847-labeled neu

65 udies of intracellular Zn2+ accumulation and double staining studies (using SMI-32 and anti-glutamate

66 Double staining studies using the neuronal marker NeuN i

67 leus caudalis (Vc), exhibited FluoroGold/Fos double staining, suggesting the activation of the trigem

68 bral arteries of the pig was investigated by double-staining techniques using combined immunofluoresc

69 clonal epithelial cells was investigated by double staining to K12 and K10 keratins.

70 P antibody IP-positive sera was confirmed by double staining using antifibrillarin monoclonal antibod

71 and ecmB genes of Dictyostelium by enzymatic double staining using beta-galactosidase and beta-glucur

72 Double staining using in situ hybridization and immunocy

73 Virtually no double staining was found for NR1 and calcitonin gene-re

74 Using double staining, we were able to show that a great major

75 under standard fixation conditions, allowing double staining when used in conjunction with other repo

76 confocal and widefield microscopy using the double staining with alpha-tubulin and centrin antibodie

77 aspect of the inner nuclear layer, which, by double staining with anti-beta-galactosidase and anti-ca

78 Double staining with anti-Cre antibody and anti-M- or an

79 ir sites of incorporation were visualized by double staining with anti-MYC, antibodies to myofibrilla

80 Double staining with antibodies directed against the neu

81 Double staining with antibodies specific for the neural

82 -RNAP antibody-positive sera was examined by double staining with antifibrillarin antibodies to evalu

83 Double staining with cell-specific markers revealed that

84 Double staining with cytochrome c immunohistochemistry a

85 Double staining with phospho-ERK1/2 and neuron-specific

86 gmentation was also observed after CIBT, and double staining with XRCC1 immunohistochemistry and term

87 n of graft derived cells was demonstrated by double-staining with neuron-specific beta-tubulin antibo