ライフサイエンスコーパス: cryostat

1 ractical, for instance for samples held in a cryostat.

2 ins were rapidly frozen and sectioned with a cryostat.

3 rneas and six human corneas with a microtome-cryostat.

4 An N(2)-cooled cryostat allows for NMR isotherm measurements at both ro

5 ll increments of NO were introduced into the cryostat and the following reactions were monitored by t

6 Cryostat and vibratome vertical sections and wholemount

7 The tissue is then sectioned using a cryostat before being dissected using an LM instrument.

8 Cryostat biopsy specimens from 27 long-term recipients b

9 of peroxo Delta 9D at 4.2 K in the Mossbauer cryostat caused the release of O(2) and the reappearance

10 digitally and thickness was determined from cryostat cross sections.

11 Furthermore, using cryostat-cut sections of I. ricinus, we show that both a

12 mount fixed tissue onto the chuck inside the cryostat during cryosectioning.

13 e counted in 5-microm sections obtained with cryostat from each harvested heart.

14 m specimens were quick frozen, then cut by a cryostat into 30-micron-thick sections.

15 pid movement of a large optically accessible cryostat is used in combination with nanosecond time-res

16 reated with H2O2 or aflatoxin B1 and then to cryostat liver sections of rats treated with aflatoxin B

17 Genomic DNA isolated from a panel of cryostat microdissected metastatic prostate adenocarcino

18 ermine the level of COX deficiency in serial cryostat muscle sections (mean age, 42.6 years; range, 3

19 lar associations of dystrophin with actin in cryostat muscle tissue sections by combining resonance e

20 sically retained by simple filtration in the cryostat of the DNP polarizer, and a pure hyperpolarized

21 ed stillborn to 85 years, were fresh frozen, cryostat sectioned, and prepared for indirect immunofluo

22 ge, 6 months to 67 years) were fresh frozen, cryostat sectioned, and prepared for indirect immunofluo

23 Immunolabeling of cryostat-sectioned eyes harvested from Abca4(-/-) mice r

24 Cryostat-sectioned tissue revealed extensive GluR 5/6/7-

25 emoved and activity was measured, lungs were cryostat-sectioned to detect the presence of ICAM-1 by i

26 Immunocytochemistry was performed on cryostat sections (14 microm) of caudal brainstem, using

27 (-IR) axons in the female rat bladder, using cryostat sections and whole wall thickness preparations.

28 cortical neurites grew robustly on neonatal cryostat sections but only sparsely on sections from adu

29 Moreover, cryostat sections can also be subjected to various treat

30 mined br radioligand binding analysis and in cryostat sections derived from normal liver and hepatoma

31 ocytes and E-cadherin on epithelial cells in cryostat sections from 34 diagnostic biopsy specimens an

32 r cortex were plated onto various regions of cryostat sections from developing and adult hamster brai

33 Labeled MSCs were observed in 5-mum cryostat sections from each harvested heart.

34 Cryostat sections from monkey brain and spinal cord were

35 Ten 30-microm cryostat sections from the macula (foveal and perifoveal

36 , we performed immunohistological studies on cryostat sections obtained from 26 breast cancer biopsie

37 njugated secondary antibody was performed on cryostat sections of 90 renal transplant biopsies, inclu

38 n both single AV nodal cells in vitro and in cryostat sections of AV nodal tissue in situ.

39 Cryostat sections of brains obtained from rats immediate

40 lls were examined by immunohistochemistry in cryostat sections of bronchial/nasal biopsies obtained f

41 uorescence (IF) for desmosomal components on cryostat sections of fresh epithelia was supported by im

42 Cryostat sections of fresh nonfixed corneas were obtaine

43 Cryostat sections of frontal cortex and subcortical whit

44 d IV activities were demonstrated in unfixed cryostat sections of gingival tissue from chronic period

45 Cryostat sections of heart and lung were prepared for in

46 l medium, neurons were cultured onto unfixed cryostat sections of mature rat CNS tissue.

47 and bind selectively to endothelial cells in cryostat sections of mouse tissues.

48 Cryostat sections of nasal/bronchial biopsies obtained f

49 rom degradation by exogenous gelatinase B in cryostat sections of nerve in vitro.

50 otein extracts in immunoblot analysis and to cryostat sections of ocular tissues in immunofluorescenc

51 focal microscopy of rat cardiac myocytes and cryostat sections of rat left ventricle papillary muscle

52 in wholemounts of urothelium or detrusor or cryostat sections of the bladder.

53 Cryostat sections of the developing brain provide a usef

54 ed using 125I-PP receptor autoradiography on cryostat sections of the entire brain cut in three plane

55 table polypeptides and their distribution in cryostat sections of the limbocorneal area were investig

56 stry were employed on paraformaldehyde-fixed cryostat sections of the pigeon eye and surrounding orbi

57 Cryostat sections of the rat hippocampus were used as ti

58 sing cells was established by immunostaining cryostat sections of the retina with antibodies against

59 Previous studies have depended on cryostat sections of tissues selected grossly.

60 Mice were injected with 125I-estrogen and cryostat sections thaw mounted onto emulsion-coated slid

61 C4d staining of cryostat sections was done by a sensitive three-layer im

62 te outgrowth from cortical explants onto the cryostat sections was visualized with a fluorescent vita

63 rain, spinal cord, and eyes were frozen, and cryostat sections were collected on slides, hybridized w

64 Five-micrometer-thick cryostat sections were cut and in situ hybridization was

65 Five-micrometer cryostat sections were cut, and in situ hybridization wa

66 Serial 50 microm cryostat sections were obtained throughout the medulla,

67 Serial 50 microm cryostat sections were obtained throughout the rostral h

68 Consecutive cryostat sections were prepared from eyes at different s

69 Whole mounts and cryostat sections were prepared from the central nervous

70 Cryostat sections were probed with antibodies directed a

71 Cryostat sections were stained for interleukin (IL)-12 o

72 ival times ranging from 10 hours to 28 days, cryostat sections were stained for routine histology and

73 Cryostat sections were taken and labeled in vitro by one

74 Corneal thickness was determined from cryostat sections, and mRNA expression was measured by r

75 was used to detect class II MHC proteins on cryostat sections, followed by computer-assisted image a

76 ction of microRNA (miRNA) and they often use cryostat sections, signal amplification and hybridizatio

77 between B16-F1 and B16-F10 melanoma cells in cryostat sections.

78 , Cx 32, Cx 43, and Cx 50 were used to stain cryostat sections.

79 fornica and Tritonia diomedea was studied in cryostat sections.

80 eat-sensitive guidance cues preserved in the cryostat sections.

81 mated using image analysis of serial coronal cryostat sections.

82 0(6) in ultra-clean nanotube resonators at a cryostat temperature of 30 mK, where we define Q as the

83 gn and construction of a novel liquid helium cryostat that accommodates variable-sized quartz tubes/c

84 Cryostat tissue sections of fixed rhesus monkey ciliary,

85 t neuropil and glia were microdissected from cryostat tissue sections of histologically severely affe

86 Cryostat tissue sections of the lids were stained by imm

87 ections of medulla from female rats cut on a cryostat were incubated with five concentrations of (125