ライフサイエンスコーパス: filter paper

1 ng cells were then liquid-dried on strips of filter paper.

2 otting 50-mul aliquots of whole blood on 903 filter paper.

3 hylsiloxane; PDMS) dissolved in hexanes onto filter paper.

4 se, bacterial microcrystalline cellulose and filter paper.

5 ght was controlled by shading a leaflet with filter paper.

6 could reach the target digestion of 4.5% on filter paper.

7 coating the encapsulated enzyme on cellulose filter paper.

8 t may affect the spreading of blood onto the filter paper.

9 r microscopic examination and blood spots on filter paper.

10 duals by ELISA using eluted dried blood from filter paper.

11 nd heat transfer of patterned wax paper onto filter paper.

12 TFN (65.71%) filter papers compared to W-903 filter paper.

13 ding a coloured compound on the surface of a filter paper.

14 assay was created by use of wax printing on filter paper.

15 pot test/diffuse reflectance spectroscopy on filter-paper.

16 ultifold towels, and Whatman numbers 1 and 3 filter papers.

17 of nucleotides in the case of DEAE cellulose filter papers.

18 HIV-1 DNA in infant blood samples stored on filter papers.

19 s were used instead of more common adsorbent filter papers.

20 tinent, as judged by random urine leakage on filter paper (4-fold higher spotting, P<0.01; 2.5-fold h

21 fficiency (100%) compared to W-903 and A-226 filter papers (91.7%) and appeared more sensitive in det

22 monitor BP disease activity using a piece of filter paper, a wax-printer, and NC16A antigens.

23 68, and this enzyme showed slightly improved filter paper activity and binding to BMCC but otherwise

24 effect of microcystins (MCs) on earthworms, filter paper acute toxicity test, avoidance test and a 1

25 (SERS) substrate platform based on a common filter paper adsorbed with plasmonic nanostructures that

26 luated two additional commercially available filter papers, Ahlstrom grade 226 (A-226) and Munktell T

27 quoted precisely 20 microL serum per spot on filter paper, air-dried the spots, and placed them in ai

28 Filter paper, although used in epidemics, needs evaluati

29 x 10(-6) to 1 x 10(-5) for a second type of filter paper, an effect not observed for materials teste

30 lectrode consists on platinum sputtered on a filter paper and a Nafion membrane to immobilize the enz

31 in very small volumes of blood collected on filter paper and can be applied to large-scale studies.

32 rom 1 x 10(-6) to 5 x 10(-6) for one type of filter paper and from 1 x 10(-6) to 1 x 10(-5) for a sec

33 ify HIV-1 gag DNA from blood spot samples on filter paper and from corresponding viably frozen mononu

34 assay, pieces of conjunctiva were placed on filter paper and incubated for 15 to 120 minutes, with o

35 his assay, with adsorption of whole blood to filter paper and no specimen processing, provides a prac

36 ), hydrolysates are filtered through ashless filter paper and pH values are adjusted with hydrochlori

37 chitosan and alginate polyelectrolytes onto filter paper and physically entrapping the tyrosinase en

38 gest that transport and storage of plasma on filter paper and quantification of HD p24 Ag may be a re

39 or faecal contamination, can be collected on filter paper and stored for many months frozen or lyophi

40 ples (n = 71) that were spotted and dried on filter paper and stored frozen (2 d).

41 PBMCs were filtered onto glass-fiber filter paper and the radioactivity was determined by sci

42 by PCR; and (iii) compression of the swab on filter paper and, after DNA concentration, testing by PC

43 thods (freezing, lyophilising, blotting onto filter paper); and freeze-thaw cycles.

44 pecimens of whole blood and plasma stored on filter paper, and of plasma stored in tubes, was compare

45 O-1 adsorbed readily on the glass microfiber filter paper, and prolonged the interaction between DNA

46 Saliva was collected using small strips of filter paper, and virus was detected using a real-time q

47 noculum size, microbial permeability through filter papers, and ability to exclude vaginal epithelial

48 Dried blood spot (DBS) samples on filter paper are surging in popularity as a sampling and

49 VL) testing and HIVDR genotyping using W-903 filter paper as a comparison group.

50 ture for office practice based on the use of filter paper as a solid-phase dilution device.

51 tivity using the blood sample deposited onto filter paper as the assay medium, by predepositing N-bio

52 rent reliable bioanalytical procedures using filter paper as well as novel volumetric microsampling t

53 ant further investigation of A-226 and M-TFN filter papers as specimen collection devices for HIVDR m

54 IgM FEIA is a potential alternative to other filter paper assay for toxoplasma-specific IgM currently

55 of wild-type adult or cord blood dried onto filter paper at levels significantly higher than that me

56 We have developed a filter paper-based nucleic acid assay, which is able to

57 The filter-paper-based sensing strips could provide reproduc

58 opment of a novel, inexpensive, and portable filter-paper-based strip biosensor for the detection of

59 In conclusion, a filter-paper-based strip biosensor was developed that al

60 ts of tests using paired reconstituted dried filter paper blood spot (DBS) samples to assess the feas

61 survey, haemoglobin density was measured and filter paper blood spots were collected to determine age

62 nsitive than currently used PCR methods from filter paper blood spots.

63 m influx can be measured by application of a filter paper blotter saturated with a 45Ca-labeled buffe

64 All mutant enzymes with lower activity on filter paper, BMCC, and SC had lower processivity.

65 er by cell wall extension or by weakening of filter paper but hardly affected binding to whole cell w

66 pecific adsorption of a range of proteins to filter paper by at least 1 order of magnitude without si

67 routinely collected from newborn babies onto filter paper called Guthrie cards and used to screen for

68 in very small volumes of blood collected on filter paper cards and can be applied to large-scale epi

69 ble for at least 147 days when stored on DBS filter paper cards at room temperature in the dark.

70 The filter paper changed color based on concentration of glu

71 lative humidity sensor was developed using a filter paper coated with nanoparticles, which could easi

72 inent genotyping information: oral fluid and filter paper collection methods.

73 vities for A-266 (71.54%) and M-TFN (65.71%) filter papers compared to W-903 filter paper.

74 RNA values from filter paper, corrected for the hematocrit, gave results

75 h plasma and whole-blood specimens stored on filter paper correlated with plasma HIV-1 RNA levels (Sp

76 by a solid salt-saturated filament material (filter paper, cotton textile).

77 of whole blood extraction conditions on DBS filter paper cut-outs was first achieved to maximize rec

78 The sensitivity and specificity of the filter paper dilution system for detection of high-count

79 teriuria (<10(4) CFU/ml) was detected by the filter paper dilution system in five of nine specimens (

80 In addition, the filter paper dilution system was able to detect gram-neg

81 The filter paper dilution system was compared to the standar

82 isms in urine specimens were excluded by the filter paper dilution system.

83 thetized and alkali burns created with 10-mm filter paper discs (1 N NaOH for 2 minutes).

84 is methodology consists on the use of precut filter paper discs where large amounts of sample can be

85 uid specimens that have been inoculated on a filter paper disk and placed on agar growth medium.

86 udy a new test, the AmpC disk test, based on filter paper disks impregnated with EDTA, was found to b

87 The recovery of cocaine from Teflon wool, filter paper, drug-fortified hair, and drug user hair wa

88 The DNA remained bound to the filter paper during PCR amplification.

89 Collection on filter paper followed by quantitative PCR could be usefu

90 The storage of specimens on filter paper for 2 weeks at 37 degrees C, 24 degrees C,

91 t decrease after storage of the standards on filter paper for 3 months at room temperature or after i

92 In parallel, blood samples were collected on filter paper for polymerase chain reaction (PCR) analyse

93 erformed similarly to DBS collected on W-903 filter paper for quantitative VL analysis and HIVDR dete

94 The immobilization potential of filter papers for DHBV was examined, and the highest yie

95 hyl cellulose (CMC), swollen cellulose (SC), filter paper (FP), and bacterial microcrystalline cellul

96 Blood samples were collected on filter papers from 1981 to 1984 and from 1987 to 1989 fr

97 than 9400 blood specimens were collected in filter papers from all inhabitants at baseline and then

98 pe 1 (HIV-1) DNA in whole blood collected on filter paper (FTA Card) was evaluated.

99 PCR after DNA extraction from filter paper had a sensitivity similar to that of conven

100 DBS collected on M-TFN filter paper had the highest genotyping efficiency (100%

101 osed for 6 days to 0.2 mug/cm(2) of CL-20 on filter paper, half of which were allowed to recover in a

102 Collection of serum and blood samples on filter paper has been used to screen for metabolic disor

103 The use of blood samples stored on filter paper has many advantages for the detection of pe

104 logy, bloodspot sampling by fingerstick onto filter paper has many advantages, including ease and low

105 plasma samples that are spotted and dried on filter paper have been shown to provide reliable and acc

106 Dried blood spots (DBS) collected onto filter paper have eased the difficulty of blood collecti

107 e to insoluble reducing sugar produced after filter paper hydrolysis by E4-90, E4-68, E4-74, and E4-5

108 ophilic optical pH indicator) are printed on filter paper in the absence of any plasticizer and/or ad

109 better understanding of reagent stability on filter paper is critical for proper device use and its l

110 The filter paper is maintained in a small circular heated ov

111 Currently, Whatman 903 (W-903) filter paper is the only filter paper that has been used

112 ysis, but blood from a fingerstick placed on filter paper (known as dried blood spots (DBS)) is more

113 ghest sensitivity is achieved by testing the filter paper lysate in quadruplicate.

114 Additionally, the use of common filter papers makes it a simpler and more rapid alternat

115 The filter paper material allows for transport by capillary

116 Bloodspot sampling by fingerstick onto filter paper may increase the feasibility of large-scale

117 tion of ISEs based on commercially available filter paper modified with single-walled carbon nanotube

118 An alkali injury was produced with a filter paper of 3 mm with 1 N NaOH during 40 seconds on

119 microbial concentration and ZOI, when either filter paper or corneal discs were used (R(2) > 92%).

120 DBS collected on A-226 and M-TFN filter papers performed similarly to DBS collected on W-

121 Bacterial colonies were smeared onto filter paper precut to a sharp point, then wetted with s

122 e carriage density in samples extracted from filter paper ranged from 1 to 25,000 DNA copies.

123 ifferent distribution of the analytes on the filter paper, rendering obtaining reliable quantitative

124 of DNA present in blood, dried and stored on filter paper samples.

125 PCR results with blood from filter papers showed 100% specificity (95% confidence in

126 Collection of biological fluids on clinical filter papers shows important advantages from a logistic

127 Collecting whole blood on filter paper simplifies the processing, transport, and s

128 ported by localized pH experiments, in which filter paper soaked in various buffers was applied to on

129 port prepared in the form of small (4 x 4mm) filter paper squares.

130 using immobilized glucose oxidase enzyme on filter paper strip (specific activity 1.4 U/strip) and t

131 onjunctival cells obtained by nitrocellulose filter paper stripping (impression cytology).

132 ion, conjunctival epithelium was obtained by filter paper-stripping from the bulbar temporal region f

133 CF was sampled from 6 sites per subject with filter paper strips and PGE2 levels measured using an en

134 was sampled from 12 intrasulcular sites with filter paper strips for the measurement of six types of

135 Filter paper strips soaked in solutions of the test mole

136 l surfaces of premolar and molar teeth using filter paper strips.

137 1 cellulose filter paper strips.

138 ing its sensitivity toward La(3+) on Whatman filter paper strips.

139 fresh or pretreated cells were spotted onto filter paper strips.

140 se delivery of a small volume of sample to a filter paper substrate, assisted by a flow-injection-lik

141 e activity on acid-swollen cellulose than on filter paper, suggesting that this mutation affected the

142 bacterial microcrystalline cellulose (BMCC), filter paper, swollen cellulose, and carboxymethyl cellu

143 ition, we measured ASL composition using the filter paper technique.

144 No acute toxicity was found in the filter paper test, and earthworms showed no avoidance re

145 Whatman 903 (W-903) filter paper is the only filter paper that has been used for HIV load and HIV dru

146 Whole blood was collected on filter paper that lysed cells and bound the DNA, elimina

147 However, in synergistic assays on filter paper, the addition of Cel48A to a balanced mixtu

148 By integrating the APTMS-GA complex with filter paper, the modified paper enables quantitative de

149 ially treat the opposing surfaces of a glass filter paper to enable this unique capability.

150 hene nanoplatelets (GP) suspension coated on filter paper to increase the sensitivity of the immune r

151 infection, and blood spots were collected on filter paper to test for antibodies to Chlamydia trachom

152 We compared whole blood dried on filter paper to the standard assay with frozen cell-free

153 was extensively used for the modification of filter papers to develop paper based analytical devices.

154 on nanotubes ink) is applied on conventional filter papers to turn them into conductive papers, which

155 ry materials, such as disposable pipet tips, filter paper, tooth picks, and nylon mesh.

156 ke of ozone to five materials: two cellulose filter papers, two cementitious materials, and an activa

157 The stability of p24 Ag on filter paper under conditions simulating specimen transp

158 We demonstrate that a common laboratory filter paper uniformly adsorbed with biofunctionalized p

159 0 mg proteing glucan(-1) [ approximately 6.5 filter paper units (FPU)], revealing that the enduring f

160 and glucose oxidase were coimmobilized onto filter paper using a silanization procedure.

161 reconstituted antibodies that were stored on filter paper using flow cytometry.

162 pectively) particles isolated from cellulose filter papers via acid digestion were characterised and

163 cificity of the HD p24 Ag assay of plasma on filter paper was 100%, the specificity was diminished in

164 line and eosin at pH 7.5 in Tris; a piece of filter paper was used as a solid support and solid fluor

165 y was similar when plasma and whole blood on filter paper were contrasted to the real-time RT-PCR ass

166 Pieces of filter papers were coated with starch-iodine solution le

167 Whatman filter papers were used not only as support for electrod

168 Four MFCs were prepared on a T-shaped filter paper which was eventually folded three times to

169 (bias = -0.028 +/- 0.186 log(10) copies/ml) filter papers, while qualitative VL analysis for virolog

170 hilic reagent zones were defined by printing filter paper with a hydrophobic paper sizing agent using

171 The donor and acceptor layers are made of filter paper with a printed pattern.