ライフサイエンスコーパス: standard curve

1 .5--> 527.5 transition of IS to generate the standard curve.

2 hence the isoform ratio by reference to the standard curve.

3 o be 33 and 39% ON, respectively, by using a standard curve.

4 y reproducing the colorimetry-obtained ELISA standard curve.

5 tration is determined without the need for a standard curve.

6 red and non-linear, resulting in an unusable standard curve.

7 ted to quantify sample concentration using a standard curve.

8 unknown samples could be extrapolated from a standard curve.

9 plification are correlated by an exponential standard curve.

10 entration was calculated from an appropriate standard curve.

11 is time frame also improved linearity of the standard curve.

12 d analyte, as an internal standard against a standard curve.

13 gene usually by relating the PCR signal to a standard curve.

14 of each protein isoform by reference to the standard curves.

15 -739), and IS peptides were used to generate standard curves.

16 results may be obtained without the need for standard curves.

17 ked-in proteins of known amounts to generate standard curves.

18 hich led to a desired transition pH based on standard curves.

19 specific RPL19 primers were used to generate standard curves.

20 ful for quantification based on promastigote standard curves.

21 es were converted to concentrations by using standard curves.

22 itation can be achieved without reference to standard curves.

23 encies of plasmid and cellular environmental standard curves (98 and 100%, respectively) allowed obta

24 A standard curve, and (iv) external (13)C PA standard curve, all agreed within 1 digit in the same or

25 d on back-calculated adduct masses from five standard curves analyzed over a four-week period.

26 In a set of experiments in which the standard curve and algorithm were used to analyze and qu

27 antiserum shifted the double antibody assay standard curve and altered estimates of assay specificit

28 al relative quantification using an internal standard curve and need for calibrant diluent, and takes

29 etection, we were able to generate an in-gel standard curve and quantitate total disulfide contents w

30 ential decay equation best fit the universal standard curve and strain-specific curves (R2 of 0.96 an

31 Pork DNA standard curves and cycle threshold (Ct) values were use

32 ope one-point calibration, (iii) external PA standard curve, and (iv) external (13)C PA standard curv

33 t methods (absolute standard curve, relative standard curve, and comparative C(T)) and show them to b

34 he universal standard curve, each subgroup's standard curve, and strain-specific curves were +/-0.87,

35 ally adequate sample numbers, an appropriate standard curve, and the inherent quantitative capacity o

36 rect assay can be corrected for by using the standard curve appropriately.

37 Standard curves are linear over a 10(3)-fold concentrati

38 Standard curves are linear over a 100-fold concentration

39 Linear standard curves are reported for a variety of compounds

40 h fiber and by comparing results to a single standard curve based on toxin in buffer.

41 the number of GMOs has increased over time, standard-curve based simplex quantitative polymerase cha

42 Standard curves between 0.04 and 10.00 nmol curcumin wer

43 1% and accuracy between 93.8 and 107% at the standard curve concentration range.

44 from the sample absorbance and the reference standard curve constructed from the reference concentrat

45 d densitometry and threshold cycle data, the standard curve constructed from threshold cycle data had

46 3'TAMARA-labeled probe in comparison with a standard curve constructed with known copy numbers of it

47 Standard curves could be generated using absolute intens

48 measured by this method was 20 nM, with the standard curve covering a wide range (7.8-32,000 nM).

49 and recipient colonies were estimated from a standard curve created by LEW and BN bone marrow mixture

50 lied to the fillets were estimated using the standard curve data obtained from the correlation values

51 Results were quantitated by using a standard curve derived from a plasmid containing IS900.

52 abinitol concentrations were calculated from standard curves derived from pooled human serum containi

53 rtainty is a result of the highly uncertain "standard curve" developed during each test and (2) the u

54 for log(10) estimations using the universal standard curve, each subgroup's standard curve, and stra

55 yonic stem cell RNA) and measured associated standard curves, efficiency (57%), repeatability (~1 cyc

56 by comparing the mass signal integrals to a standard curve established using purified recombinant PS

57 This algorithm estimates standard curve features as well as nucleic acid concentr

58 The standard curve fitted linearly (R(2) = 0.9982) and allow

59 paper, a method for estimating n and Kd from standard curve-fitting procedures is established.

60 A standard curve for detection of cortisol in saliva was g

61 rted for DNA methylation, but they require a standard curve for quantification or only show moderate

62 The standard curve for the drug pazopanib was falsified to m

63 ed DENV and CHIKV RNAs were used to generate standard curves for absolute quantification.

64 photoluminescence microwell imager, and the standard curves for each analyte were quantified from th

65 The standard curves for each chondroitin disaccharide showed

66 Standard curves for each isoform demonstrated good sensi

67 Standard curves for nanomolar concentrations of ADP, UDP

68 led standard peptides, to construct internal standard curves for peptides derived from key nodes in s

69 in RNA-seq experiments as well as to derive standard curves for quantifying the abundance of transcr

70 Standard curves for S1P and DHS1P are linear over wide r

71 r absolute quantification when compared to a standard curve from the same Leishmania species.

72 Standard curves from 50 to 10,000 ng/mL are generated.

73 d ([(13)C(3)]malonyl-CoA) and multiple-point standard curves from 50 to 1000pmol.

74 ion that automatically generates calibration standard curves from series of standards that can be use

75 All standard curves generate by this method had coefficients

76 of the genome copies is extrapolated from a standard curve generated from amplification of quantifie

77 applied to the tissue was determined using a standard curve generated from MALDI time-of-flight (TOF)

78 The standard curve generated from the chip consisted of two

79 the SSB yields per DNA molecule, employing a standard curve generated using DNA molecules containing

80 ns from environmental samples using absolute standard curves generated by real-time qPCR.

81 Standard curves generated for each metabolite have corre

82 Standard curves generated suggested good linear relation

83 Even standard curves generated using free 7-amino-4-methylcou

84 molar concentrations, were interpolated from standard curves generated with synthetic peptides that c

85 ract can be obtained in less than 2 h once a standard curve has been prepared for H4PteGlun.

86 including absolute quantification without a standard curve, improved precision, improved accuracy in

87 , underscore the importance of preparing the standard curve in the same matrix as the unknown sample

88 A reproducible standard curve is generated with a EC(50) of approximate

89 tissue homogenates (10 ng/g tissue), and the standard curve is linear up to 1000 ng/mL, with precisio

90 lute concentration of target sequence when a standard curve is not available.

91 receptors, but also the medium in which the standard curve is run.

92 ernal standards DA-d4 and DOPAC-d5 result in standard curve linearity for DA from 0.05-100 ng/mL (LOD

93 two methods of calculating fold increase: a standard curve method and the DeltaDelta Ct method.

94 gene copy numbers were achieved by relative standard curve methods using cloned C4 genomic DNA cover

95 Further, we conducted a series of standard curve migration assays for basal media suppleme

96 us in all samples was quantitated by using a standard curve obtained by serial dilution of an in vitr

97 After comparison with standard curves obtained by serial dilution of DNA extra

98 Standard curves obtained from 2-ml aliquots of BAL fluid

99 oreover, in an experiment directly comparing standard curves obtained from band densitometry and thre

100 Islet sizes were extrapolated from standard curves obtained using microspheres from which i

101 A standard curve of band densities was generated by using

102 ody levels were determined by reference to a standard curve of fluorescent intensity generated using

103 Based upon a TaqMan-generated standard curve of infectious WN virus, the limit of dete

104 A standard curve of Leu-enkephalin was performed in the pr

105 3.0 values of <50 copies/ml by extending the standard curve of the assay showed that these samples wi

106 By comparison with a known standard curve of tm versus log[Na+] for poly(dA) . poly

107 Standard curves of antibiotic concentration versus ECL i

108 ion, integrated ion counts were derived from standard curves of authentic compounds of phosphatidylch

109 Standard curves of neat authentic standards and spiked e

110 new method was developed for preparation of standard curves of spiked tissue homogenates, based on t

111 Standard curves of the spiked calibrants were generated

112 g SPSS V 16.0 (P < 0.05) and quantified with standard curve on GCDC acid.

113 Use of a potato starch standard curve over-estimated starch concentrations.

114 ] vs 69 [56-87]% of maximum concentration in standard curve; p=0.043; n=8 and n=6, respectively).

115 The average accuracy for the standard curve points in extracted human plasma was 99-1

116 A standard curve prepared for methylphenidate in urine (R(

117 enrichments were calculated by comparison to standard curves prepared from dA and [(2)H(2)]-dA.

118 Internal bovine serum albumin standard curves provided a method to assess on-chip PF2D

119 otal RNA concentrations and agrees well with standard curve qPCR.

120 quantification by SQT-DNA is as reliable as standard curve quantification for a wide range of DNA co

121 m 15 to 30% at all concentrations within the standard curve range.

122 area ratios at all concentrations within the standard curve ranges were compared.

123 data using three different methods (absolute standard curve, relative standard curve, and comparative

124 The software estimates standard curves, sample protein concentrations and their

125 The resulting standard curves showed good linearity and high sensitivi

126 For these assays, standard curves showing correlation between target conce

127 f infectious virus/reaction) and efficiency (standard curve slope = -3.66).

128 Precision values of standard curves slopes were lower than 3.4% and recovery

129 shed to be 31.25pM with the linearity of the standard curve spanned to 2500pM.

130 The qualified range of the standard curve spans 6 orders of magnitude from 2.5 x 10

131 LysA cDNA detection varied linearly across a standard curve that matched the sensitivity of quantitat

132 calculated from the regression equation of a standard curve that was generated by plotting the logari

133 nalyses of these assays use methods based on standard curves that have limitations in detecting low o

134 eiver operating characteristic (ROC) curves, standard curves that represent item recognition across d

135 rived relationship to generate a theoretical standard curve, the measured ratio of the M (monoisotopi

136 Based on a linear standard curve, the species' absorbance at 1104 cm(-1) i

137 Based on these data, a standard curve up to 2.5muM Cyt c was established.

138 inescent assay was conducted by developing a standard curve using known concentrations of PSA.

139 Standard curves using four different bacterial species g

140 ti-PS2 immunoblot signals by comparison with standard curves using radiolabeled PS1 and PS2 standards

141 A method was developed for creating standard curves using surrogate tissue sections from bla

142 Standard curves utilized both extractions from RSV cultu

143 There were negligible readings for standard curves utilizing copper in place of iron.

144 A standard curve was constructed showing a large range of

145 these fluorescence intensities, an in vitro standard curve was created based on the in vivo exposure

146 The standard curve was established from QCM-D responses and

147 A standard curve was generated and developed with TaqMan(R

148 leimide-activated bovine serum albumin and a standard curve was generated for each blot.

149 adenine was 0.02 microM (2.4 ng/ml), and the standard curve was linear up to 27.3 microM.

150 A linear standard curve was obtained between 10(1) and 10(8) DNA

151 omplex, multidimensional abundance corrected standard curves was thereby avoided.

152 The linearity of standard curves was up to 5000 pM.

153 Final standard curves were calculated for each pathogen by plo

154 Standard curves were constructed (R(2)>0.99) to allow fo

155 Standard curves were created for alginate in deionised H

156 After standard curves were developed for quantification of C1-

157 Standard curves were established by relating the MGIT ti

158 The standard curves were fitted to a quadratic regression ov

159 Full standard curves were generated for 23 different assays.

160 CFU estimations by all three standard curves were highly reproducible, regardless of

161 In fact, the raw data for the standard curves were highly scattered and non-linear, re

162 Standard curves were linear from 25 fmol to 2 pmol for p

163 Opiate standard curves were linear from the LOQ to 12500 pg/mg.

164 Standard curves were linear from the LOQ to 5000 pg/mg f

165 Standard curves were linear over a range of 0.0 to >4.5

166 Standard curves were linear over a range of 5-1000 ng fo

167 The standard curves were linear over the range from 2 ng/mL

168 400 ng/mL), good linearities (r2 > 0.99) for standard curves were obtained.

169 LightCycler Q-PCR conditions, we obtained a standard curve with a linear range (correlation coeffici

170 ed from the observed ion intensities using a standard curve with curve parameters unaffected by the p

171 lysates were then determined by generating a standard curve with defined amounts of a highly purified

172 d as a surrogate matrix for human to prepare standard curves without endogenous interference.