ライフサイエンスコーパス: double staining

1 lymphocytes were proliferating (assessed by double staining).

2 idization, and immunocytochemical single and double staining.

3 sed in flow cytometry and immunofluorescence double staining.

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

5 Apoptosis was quantified using double staining.

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

7 Double staining and confocal microscopic analysis reveal

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

9 In a double staining approach, we simultaneously measured OSN

10 Double staining confirmed that both the conformation-spe

11 Immunohistochemistry and double staining confirmed the expression of FcRn recepto

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

13 Immuno-double-staining experiments in Saccharomyces cerevisiae

14 Histochemical analysis (double staining for alkaline phosphatase and dipeptidyl

15 Double staining for cardiomyocytes with alpha sarcomeric

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

17 Double staining for Dmp1 and Ki67 revealed that these tw

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

19 Double staining for host macrophages and SPIO particles

20 Double staining for Luxol fast blue and Bielshowsky was

21 Double staining for oxytocin or vasopressin neurons reve

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

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

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

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

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

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

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

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

30 Immunofluorescence double-staining further confirmed a notable reduction in

31 We used double staining histochemistry to investigate the relati

32 Double staining IHC showed that axonal terminals of both

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

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

35 Double staining immunofluorescence was used to label uPA

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

37 Double-staining immunofluorescence studies showed coloca

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

39 Double staining immunohistochemistry was also used to in

40 Double staining immunohistochemistry was employed to eva

41 Double-staining immunohistochemistry showed CXCL9 co-loc

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

43 The double staining in the flatmounted retinas demonstrated

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

45 Significantly, ex vivo double staining indicated that compound 37 detected Abet

46 Immunofluorescence double-staining, ligand binding, and Scatchard plot anal

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

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

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

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

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

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

53 Double staining of native eve protein and transgene mRNA

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

55 Anterograde double staining of the antennal afferents revealed that

56 Double staining of transgenic mouse brain sections with

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

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

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

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

61 Double staining revealed that these cells were distinct

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

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

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

65 Double staining showed that activated macrophages/microg

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

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

68 Double staining showed that suppression of c-fos express

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

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

71 Double staining studies using the neuronal marker NeuN i

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

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

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

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

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

77 Double staining using in situ hybridization and immunocy

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

79 Flow cytometry based-Annexin V-FITC/PI double-staining was used to further quantify cellular vi

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

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

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

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

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

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

86 Double staining with antibodies directed against the neu

87 Double staining with antibodies specific for the neural

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

89 Double staining with cell-specific markers revealed that

90 Double staining with cytochrome c immunohistochemistry a

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

92 Subsequent analyses using double staining with specific cell markers noted the enr

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

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