ライフサイエンスコーパス: fM

1 sDNA-T concentration over the range from 1.0 fM to 1.0nM, with a detection limit of 0.47 fM, can be o

2 the t-ssDNA concentration in a range of 1.0 fM to 10 nM under optimized conditions.

3 eprotonated prior to Zn(II) binding, the 1.0 fM Zn(II)-GGG Kd value reflects a Zn(II) complexation re

4 tration of the target miRNA ranging from 2.0 fM to 8.0 pM, and the detection limit was 0.6 fM.

5 0 fM to 2.0 pM with a detection limit of 2.0 fM.

6 ing (~435 fold) the detection limit from 3.0 fM (without NSs labeling) to 6.9 aM (with NSs labeling).

7 ation of target DNA in a wide range from 5.0 fM to 1.0 pM.

8 iling can be performed label-freely from 5.0 fM to 2.0 pM with a detection limit of 2.0 fM.

9 Assay linear range was from 50.0 fM to 1.0 nM, with a limit of detection of 1.72 fM.

10 se concentrations ranged from 0.76 fM to 6.0 fM showed that cluster number has a linear relationship

11 ing its detection at a concentration of 0.01 fM, five orders of magnitude lower than that detectable

12 Low concentrations of melatonin (0.01 fM-1 PM) inhibited forskolin (100 microM)-stimulated cAM

13 e with the detection limit estimated as 0.03 fM (S/N=3.0) and 0.08 fM (S/N=3.0) for 20-mer ssDNA and

14 OD of 1300 bacteria per 50 muL sample (0.042 fM).

15 an average limit of detection (LOD) of 0.07 fM, or 2100 DNA molecules per 50 muL sample.

16 OD of 1100 bacteria per 25 muL sample (0.074 fM), and (b) water from the Charles River, with an LOD o

17 imit estimated as 0.03 fM (S/N=3.0) and 0.08 fM (S/N=3.0) for 20-mer ssDNA and for dsDNA (PCR product

18 at subfemtomolar levels ( approximately 0.08 fM).

19 ient of 0.999, a detection limit between 0.1 fM and 0.5 fM, and a linear dynamic range of over 500-fo

20 (ssDNA) concentrations in the range from 0.1 fM to 0.1 nM with a low detection limit of 62.41 aM, and

21 ch, the detection limit of miRNA-122 was 0.1 fM via direct readout, with a wide detection range from

22 Melatonin (0.1 fM-1 nM) inhibited forskolin-induced cAMP formation in a

23 +) (Site I K(a)=1.3 fM(-1), Site II K(a)=1.1 fM(-1)), in conjunction with reversible direct Cu(+) tra

24 lue for ANG with the deletion variant is 1.1 fM, only 2-fold higher than with WT RI.

25 cid complexes were determined to be 15 +/- 1 fM and 33 +/- 8 fM, respectively.

26 hese values for k(1) and k(-1), was 15 +/- 1 fM.

27 otein, reaching a detection limit of 4 +/- 1 fM in buffer and 10 +/- 2 fM in 10-fold diluted nasophar

28 n of the enzyme inhibitor, which is around 1 fM.

29 The Scano-miR system was able to detect 1 fM concentrations of miRNA in serum with single nucleoti

30 ors were able to detect glycoproteins from 1 fM (Con A), 10 fM (Ricinus communis agglutinin (RCA), or

31 reases upon hybridization (signal on) from 1 fM to 1 nM of target miRNA.

32 monstrates a very wide dynamic range (from 1 fM to 1 nM).

33 /- 2.1% for target DNA concentrations from 1 fM to 10 fM, while a capacitance increase was observed w

34 20s and exhibits a large linear range from 1 fM to 10 pM, with a limit of detection (LOD) of 152.93 a

35 n of 0.37 fM and a wide dynamic range from 1 fM to 100 nM along with clear distinction from mismatche

36 nin (Ang) with extraordinary affinity (Ki <1 fM).

37 to detect ssDNA down to a concentration of 1 fM in a volume of 25 muL (25 zeptomoles).

38 complementary strands at concentrations of 1 fM, 1 pM, and 1 microM, both separately and sequentially

39 tude and provided detection limits down to 1 fM (28.5 fg/mL).

40 ted within the dynamic range from 10 aM to 1 fM and detect as low as 2 aM of miR-122 ( approximately

41 235, 419, and 1613 nucleotides at 1 pM to 1 fM and found that the LOD decreased as DNA length increa

42 early discriminated and detection limit to 1 fM range is observed.

43 Detection sensitivity of up to 1 fM was demonstrated for the Raman labels chosen to clear

44 Sensor hybridization responses to 1 fM, 1 pM, and 1 microM complementary strand were nearly

45 ion sensitivity in sandwich assays down to 1 fM--a three-order-of-magnitude improvement over most rep

46 itivity allowed us to detect unprecedented 1 fM Hg ions in 20 min in field samples treated by simple

47 Detection of SNPs down to 0.10 fM is realized by measuring the conductance of the nanog

48 o detect glycoproteins from 1 fM (Con A), 10 fM (Ricinus communis agglutinin (RCA), or 100 fM (SNA) w

49 tection limit is investigated to be 1 and 10 fM for miR-204 and miR-210, respectively.

50 n with high potency: the EC(50) is around 10 fM.

51 Target DNA fragments at 10 fM concentration (approximately 6 x 10(5) molecules) wer

52 for this novel assay was determined to be 10 fM.

53 ine and a detection limit was found to be 10 fM/L (S/N=3).

54 in GABA(A)-mediated inhibition at between 10 fM and 10 nM, a response normally associated with benzod

55 as biphasic, being dose dependent between 10 fM and the peak effect at 10 pM, and inversely related t

56 gher-specificity and attained femtomolar (10 fM) sensitivity.

57 mic range spanning 6 orders of magnitude (10 fM-1 nM) with a limit of detection of less than 10 attom

58 bodies, we establish a detection limit of 10 fM for the protein IL-2, 150 times more sensitive than t

59 A detection limit of 10 fM in a 50-microL sample volume was achieved within 30 m

60 ets can be detected at a concentration of 10 fM on a single chip.

61 osited gold layer, the detection limit of 10 fM R6G solution concentration with uniform SERS effect a

62 nteractions were quantified in a range of 10 fM to 100nM.

63 voltammetry enabled a detection limit of 10 fM to be reached with good reproducibility.

64 tect unmodified DNA at a concentration of 10 fM.

65 led DNA targets with a detection limit of 10 fM.

66 RU34347 (10 fM-10 nM) produced an increase in GABA(A)-mediated inhib

67 y showed excellent detection sensitivity (10 fM) and specificity and was demonstrated for quantitativ

68 ssociation constant: biotin/streptavidin (10 fM) and HER2/HER2 antibody (0.44 +/- 0.07nM), respective

69 With this assay, detection limits down to 10 fM and 1 pM were achieved for proteins and target DNA, r

70 t insulin with limit of detection down to 10 fM in both buffer solution and diluted human serum witho

71 or target DNA concentrations from 1 fM to 10 fM, while a capacitance increase was observed when H5 ta

72 mixture of analytes ranging from 1 nM to 10 fM.

73 ction, lowers the detection limit down to 10 fM.

74 3 nucleotide oligomers detectable down to 10 fM.

75 orders of magnitude, from approximately 100 fM to 100 nM.

76 BP (FRB.rapamycin+FKBP, Kd approximately 100 fM; FKBP.rapamycin+FRB, Kd = 12 nM).

77 cted at initial concentrations as low as 100 fM by using a combination of field-amplified injection a

78 NA sequences at concentrations as low as 100 fM in 500 muL.

79 It permits detection of as low as 100 fM trigger oligonucleotide in under 10 min total assay t

80 gets present at concentrations as low as 100 fM using the two-color assay.

81 ere detected at concentrations as low as 100 fM, corresponding to <1 muL of perfluorocarbon per liter

82 dic peptides at concentrations as low as 100 fM.

83 e to enable human CDK2 to be detected at 100 fM or 5 pg/mL, well within the clinically relevant range

84 evels of circulating TF, whole blood (+/-100 fM added TF) was tested under static and flow conditions

85 We demonstrate that we can detect 100 fM dual-labeled DNA diluted in 1 microM unlabeled DNA, w

86 stimulated with a high (100 muM) or low (100 fM) dose of cognate antigen.

87 limits were demonstrated down to nearly 100 fM, which may be low enough to identify certain genetic

88 We demonstrated detection of trace of 100 fM Alexa Fluor 488 (signal-to-noise ratio of 11) with a

89 10 successive, 1-microL applications of 100 fM IgE.

90 After 5 minutes, the addition of 100 fM TF to whole blood had negligible effect under static

91 eotides (nt) and a limit of detection of 100 fM with a dynamic range of 5 decades.

92 al system, with a low detection limit of 100 fM, which is approximately 5 orders of magnitude lower t

93 M (Ricinus communis agglutinin (RCA), or 100 fM (SNA) with a linear range spanning 6 (SNA), 7 (RCA),

94 ntration of model target miRNA-21 in the 100 fM to 25.0 pM range.

95 10,000 ssDNA molecules corresponding to 100 fM thrombin in solution) by a subsequent surface RNA tra

96 of eight transistors--is achieved with a 100-fM sensitivity, on par with optical DNA microarrays and

97 probes; the insulin detection limit was 128 fM with a dynamic range of over 4 orders of magnitude in

98 idly and reliably detected up to 1 pg/mL (13 fM) concentration on PNA electrode but, as expected, yie

99 ter Hg(0) concentrations ( approximately 130 fM) observed in the Pacific intertropical convergence zo

100 imated at 100%, the limit of detection is 15 fM.

101 unambiguously detectable up to 10 pg/mL (150 fM) on PNA and SNA electrodes, respectively.

102 Sea and found low concentrations (39 +/- 16 fM) above the halocline and high concentrations in anoxi

103 35.4 nl assay volume) for target DNA and 16 fM (338 molecules) for target RNA after 1h on-chip hybri

104 with LOD values of 650 fM (160 amol) and 190 fM (50 amol) for the event-specific and the taxon-specif

105 n limit of 4 +/- 1 fM in buffer and 10 +/- 2 fM in 10-fold diluted nasopharyngeal swabs, which is com

106 he device is able to selectively detect 36.2 fM of EGFR in the total protein solution of 0.1 ng/ml ex

107 t the amperometric detection of glucose at 2 fM concentration in a physiological buffer solution at 1

108 coma cells are also sensitive to fM-GAi; (2) fM-GAi drugs only display inhibitory activity against HG

109 The detection limit is ca. 20 fM, corresponding to 6pgL(-1) diclofenac, which is compe

110 tokine interleukin-2 concentrations from <20 fM to >200 pM were demonstrated, surpassing the conventi

111 cannot exceed and is probably lower than 20 fM.

112 blood at a concentration as low as 16 to 20 fM results in pronounced acceleration of clot formation.

113 The affinity for [125I]MgTX is 100-200 fM in either Jurkat or CHO/K(V)1.3 membranes, and the re

114 cids, with limits of detection as low as 200 fM, were achieved using a capillary format with a total

115 wed a lower limit of detection (LLOD) of 200 fM and 460 fM respectively.

116 0.40 fM and a dynamic range from 1.0 to 200 fM.

117 st detection limit (DL) of 0.5 pg mL(-1) (25 fM) for IL-6 in 10 microL of calf serum.

118 ith a detection limit of 2.5 microg/mL (1.25 fM) by adopting well-designed DNA probes.

119 concentration detection limits of 270 +/- 25 fM and mass detection limits of 150 +/- 15 zmol for Chro

120 nsor provided a very low detection limit (25 fM, 0.25 attomol in 10muL sample) for miRNA-21 without a

121 he case of SPR-PI, the detection limit of 25 fM for nanoparticle-enhanced SPR-PI is approximately 20

122 eously detected at concentrations down to 25 fM using a three-sequence hybridization format that empl

123 Parathion concentrations as low as 4.26 fM are easily detected.

124 ation, with a limit of detection down to 260 fM (260 x 10(-15) M), two orders of magnitude higher tha

125 highest known engineered affinity (K(d)=270 fM) to its high affinity wild-type (K(d)=700 pM) through

126 e a limit of detection (LOD) of 10 fg/ml (28 fM) and are able to detect catalytic activity of thrombi

127 0.16 to 1.20 pM with a detection limit of 28 fM.

128 on binds AP with a calculated K(d) of </=290 fM.

129 l of ferrocene with a detection limit of 0.3 fM.

130 The lowest sensitivity corresponds to 1.3 fM in a 75 microL sample.

131 ty of these sites for Cu(+) (Site I K(a)=1.3 fM(-1), Site II K(a)=1.1 fM(-1)), in conjunction with re

132 values were calculated and found to be 26.3 fM and 62.04 m degrees , respectively, for the immobiliz

133 ith a relatively low detection limit of 84.3 fM.

134 of prostate specific antigen in buffer and 3 fM in 10% serum.

135 st limit of detection (LOD) at 100 fg/mL (~3 fM) of f-PSA in PBS solutions.

136 its of detection [LODs] ranging from 1 to 30 fM) and high specificity (distinguishing miRNAs with a s

137 ation just above the CAC ranged from 5 to 30 fM.

138 N concentration within the range of 0.01-300 fM.

139 y and specificity to tau ( approximately 300 fM) and synuclein ( approximately 300 pM) fibrils.

140 and multiplexing capabilities, detecting 326-fM concentrations of SERS nanoparticles and unmixing 10

141 the limit of detection (LOD) was 5 pg/mL (33 fM), 1,000 times better than that of ELISA.

142 hibitor of AChE, TZ2PIQ-A6 with a K(d) of 33 fM, did not distinguish between the active and OP-inhibi

143 tight (bovine Kd = 0.69 fM; human Kd = 0.34 fM).

144 ic range of EV concentration ranging from 35 fM to 35 pM, which matches the typical range of EV conce

145 ay achieved a limit of detection (LOD) of 35 fM and signals were detectable with analyte concentratio

146 the limit of detection was approximately 350 fM at the 99% confidence level.

147 is increased by a factor of >10(8), from 36 fM to >4 microM, and the selectivity factor for ANG is n

148 oncentrations in anoxic waters (1249 +/- 369 fM).

149 n of miRNA with a limit of detection of 0.37 fM and a wide dynamic range from 1 fM to 100 nM along wi

150 le detection yielded a detection limit of 39 fM (831 molecules in 35.4 nl assay volume) for target DN

151 ed 55 fM BoNT/A (1 LD50/ml) in 5 min and 0.4 fM (0.01 LD50/ml) in 5h.

152 could detect a minimum concentration of 0.4 fM DNA.

153 my at concentrations as low as 14 fg/ml (0.4 fM).

154 , the limit of detection of RNA is about 0.4 fM, which is 10 000-fold more sensitive than conventiona

155 riation (CV) across a range from nearly 27.4 fM to 1.7 pM using the described collection method.

156 of less than 10 attomoles ( approximately 4 fM).

157 ss produced a detection limit as low as 0.40 fM and a dynamic range from 1.0 to 200 fM.

158 ncentration detection limits were 520 +/- 40 fM and mass detection limits were 310 +/- 30 zmol with p

159 ) to approximately 7 pg/mL (approximately 40 fM analyte antibody concentration), and also expands the

160 were observed when as little as 40 amol (400 fM) of the desired target was present in the hybridizati

161 combination with solid-phase extraction, 400 fM digoxin was detected in 1 mL of serum.

162 ed (not extrapolated) detection limit of 400 fM, which is among the best reported for single-step ele

163 es a limit of detection of 1.2 pg mL(-1) (42 fM) PSA in 25% blood serum, which is about ten times mor

164 ogenin (Ang) and RNase A (K(D)=0.5 fM and 43 fM, respectively).

165 ited triplet state concentrations of </=0.45 fM produced by UVA and visible light irradiation of natu

166 and EHI_182030 (10 pg/mL, corresponding 453 fM) with high specificity has been achieved, employing t

167 limit of detection (LLOD) of 200 fM and 460 fM respectively.

168 fM to 1.0nM, with a detection limit of 0.47 fM, can be obtained.

169 equilibrium dissociation constant K(d) = 48 fM and slower dissociation kinetics (half-time > 5 days)

170 with angiogenin (Ang) and RNase A (K(D)=0.5 fM and 43 fM, respectively).

171 A sensitivity of 0.5 fM in 10% serum (0.1 LD50/ml serum) was attained when SN

172 99, a detection limit between 0.1 fM and 0.5 fM, and a linear dynamic range of over 500-fold.

173 s found to be linear within the range of 2.5 fM to 3.2 nM.

174 tion for this assay was determined to be 2.5 fM, and this is the first demonstration of a bar code-ty

175 Detection of concentrations as low as 5 fM proteins was obtained.

176 ngle molecules at concentrations as low as 5 fM, which is approximately a 10(3) reduction in the limi

177 The limit of quantification is ca. 5 fM.

178 of MP-Ab(2) from the SPR sensor surface is 5 fM, compared to 3-8 nM for the free antibodies.

179 red on a mAb-coated chip, a sensitivity of 5 fM (0.1LD50/ml serum) was obtained.

180 with a detection limit that corresponds to 5 fM.

181 nder optimized experimental conditions, 0.50 fM target miRNA is successfully detected.

182 magnitude by direct molecule counting; a 50 fM dual-labeled model sample can be detected with 99.5%

183 pecific detection of as little as 5 amol (50 fM in 100 muL) of target DNA.

184 er than surrounding areas ( approximately 50 fM).

185 Proteins with concentrations as low as 50 fM were detectable with 30 min of preconcentration time.

186 M and a detected concentration as low as 50 fM.

187 ling was observed when two bismuth atoms (50 fM radiolabeled antibody) were initially bound onto the

188 and had a limit of detection (LOD) of ca. 50 fM (equivalent to single molecule detection).

189 n optimized to offer a detection limit of 50 fM (0.2 amol) DNA target.

190 At present, the sensitivity limit of 50 fM is determined by the encounter rate of the labeled an

191 e quantitation of two DNA targets down to 50 fM level.

192 vity of single molecule detection down to 50 fM.

193 antification down to a level of 0.5% and 500 fM duplex DNA.

194 In contrast, femtomolar GABA (500 fM) directed a subset of GAD- vz neurons to migrate.

195 e to femtomolar concentrations of miRNA (500 fM), has a three-log linear dynamic range and is capable

196 of human thrombin at a concentration of 500 fM; the appropriate thrombin aptamer for the sandwich as

197 ection of thrombin and factor Xa at only 500 fM concentration.

198 FI-SPR provides a detection level (< or =54 fM) 2-3 orders of magnitude lower than other SPR devices

199 was toxin serotype-specific and detected 55 fM BoNT/A (1 LD50/ml) in 5 min and 0.4 fM (0.01 LD50/ml)

200 ng/mL) or 880 fmol (129 pg) for PAPR and 56 fM (9 pg/mL) or 56 zmol (9 fg) for IgG.

201 ow limit of detection (LOD) (< 5 pg/mL or 56 fM), a wide dynamic range (> 6 orders of magnitude), hig

202 the limit of detection (LOD) at 1 pg/ml (57 fM) and a linear relationship between increasing TNF-alp

203 l dissociation constant of approximately 0.6 fM.

204 M to 8.0 pM, and the detection limit was 0.6 fM.

205 The assay provides 22.6 fM sensitivity over a three log range, demonstrates mult

206 sensor demonstrates a detection limit of 6.6 fM and high selectivity when compared to other non-speci

207 f SOD1 for copper (dissociation constant = 6 fM) and the high intracellular concentrations of both SO

208 eelin displaces the high affinity (K(D) = 60 fM) binding of [(125)I]echistatin (a competitive integri

209 .1 pM to 0.10 mM) with detection limit of 60 fM.

210 lculated detection limit for this dye was 60 fM.

211 ng 365 nm excitation was determined to be 63 fM, which is 3 times lower than with the DELFIA solution

212 pM for both targets, with LOD values of 650 fM (160 amol) and 190 fM (50 amol) for the event-specifi

213 its) and an ultralow detection limit of 0.67 fM (0.012 pg/mL).

214 ound to be extremely tight (bovine Kd = 0.69 fM; human Kd = 0.34 fM).

215 M, with a detection limit of as low as 11.7 fM.

216 level by simple spectroscopic analysis (40.7 fM and 2.45fM as measured by UV-vis and dynamic light sc

217 emely high distal heme-NO affinity (K(d) ~70 fM).

218 nd a lower limit of detection of 1 pg/mL (70 fM).

219 his approach, a detection sensitivity of 700 fM (20 pg/mL) was achieved.

220 to 1.0 nM, with a limit of detection of 1.72 fM.

221 nning 7 orders of magnitude and LOD of 13.75 fM.

222 Rhodamine 6G (R6G) down to approximately 75 fM level (10(-15) molL(-1)).

223 lecules at concentrations c ranging from 750 fM (p > 90%) down to 75 aM (10(-18) molL(-1)) levels (p

224 amples whose concentrations ranged from 0.76 fM to 6.0 fM showed that cluster number has a linear rel

225 put and detects concentrations as low as 767 fM.

226 sperm can register a minimal gradient of 0.8 fM/microm and be attracted from as far away as 4.7 mm.

227 ions of 3'-MAP excited triplet states of 1.8 fM and above resulted in significant human rotavirus ina

228 with a calculated limit of detection of 22.8 fM.

229 re determined to be 15 +/- 1 fM and 33 +/- 8 fM, respectively.

230 kground noise at concentrations down to 58.8 fM with an interassay reproducibility (%RSD of n = 3) <

231 f detection = 1 pg/mL, corresponding to 58.8 fM) and EHI_182030 (10 pg/mL, corresponding 453 fM) with

232 A very low detection limit of ca. 8 fM is achieved with this sensor.

233 sence of miRNA, down to a concentration of 8 fM.

234 lytical technique with detection limit of 80 fM at concentration range up to 0.1mM.

235 s of endoglin at concentrations as low as 83 fM with high detection specificity and has a three-order

236 on limit for mediated-impact voltammetry (83 fM).

237 f n = 3) < 17.2%, and in buffer down to 5.88 fM with an interassay reproducibility (% RSD, n = 3) of

238 thod enables detection of miRNAs as low as 9 fM and allows the discrimination of one base mismatched

239 res just 30 min, with a detection limit of 9 fM (0.17 amol).

240 ommercial products with a LOD (3sigma) of 90 fM.

241 ion limit for direct-impact voltammetry (900 fM), and is more than 30 times smaller than the previous

242 re successful in detecting as little as 2.94 fM of pathogen DNA, and using crude extractions of a pat

243 The limit of detection was 6.96 fM.

244 Fluorescence bursts were measured from a fM solution of DNA fragments ranging in size from 7 to 1

245 -cone signals of opposite polarity (-sM and +fM) cancel at low frequencies, but then constructively i

246 input signals of the same polarity (+sM and +fM) sum at low frequencies, but then destructively inter

247 spite their high avidity (K(d) approximately fM, lifetime approximately 4 days), immunity protein rel

248 inhibition of HGF/SF-induced uPA activity by fM-GAi is not uncommon, in that several human tumor glio

249 min activation at femtomolar concentrations (fM-GAi) in canine MDCK cells.

250 5 mug (time-independent) of dead carbon (DC, fM approximately 0).

251 imes basal uPA activity; and (3) not only do fM-GAi derivatives strongly inhibit uPA activity but the

252 Thus, we show that certain GA drugs (fM-GAi) in an HGF/SF-dependent manner block uPA-plasmin

253 its of 100 attomolar (aM) and 10 femtomolar (fM) in pure samples for two ELISA assays with low and hi

254 vity for uranyl with a Kd of 7.4 femtomolar (fM) and >10,000-fold selectivity over other metal ions.

255 This sensor allowed femtomolar (fM) detection of FAP, a detection limit well adapted and

256 nanofiber-based system realizes femtomolar (fM) sensitivity toward complementary target DNA, and dem

257 lar calcium release channel (RyR) with high (fM) potency and provides a functional link between DDH a

258 romatic, and the fast, non-opponent inputs (+fM and +fL) as achromatic, both contribute to flicker ph

259 s in culture demonstrated that extremely low fM-nM concentrations of morphine and many other bimodall

260 he analytic sensitivity extends into the low fM concentration range.

261 cy, inducing full channel openings at lower (fM) toxin concentrations whereas at higher pM concentrat

262 4 mug (time-dependent) of modern carbon (MC, fM approximately 1) and 4.1 +/- 5.5 mug (time-independen

263 d for the non-opponent luminance mechanism (+fM and +fL) may still generate spectrally opponent signa

264 at successfully detected BPA at femto molar (fM) levels, which is an improvement over prior work by a

265 ely 5 s) and ultrahigh sensitivity (1.38 muA/fM).

266 e biosensor showed a sensitivity of 0.62 muA/fM, with a response time of 14s.

267 These effects of fM-GAi drugs on the Met-activated signaling pathway occu

268 nt with pM naloxone or naltrexone (NTX) plus fM-nM morphine blocked the excitatory effects and unmask

269 From E16 onward, two concentration ranges (fM and microM) induced motility.

270 annel has fast M- and L-cone input signals (+fM and +fL), and slow, spectrally opponent cone input si

271 eadout, with a wide detection range from sub fM to nM.

272 theory, the assay could be sensitive to sub-fM analyte because beads attached via single-immune comp

273 or ultrasensitive protein detection into the fM and aM range.

274 ons, indicating that HSP90 is not likely the fM-GAi molecular target.

275 ion by three orders of magnitude towards the fM regime.

276 en Ags are present at concentrations down to fM levels, specifically bound Abs can be scored by count

277 values in cellular assays ranging from pM to fM.

278 n leiomyosarcoma cells are also sensitive to fM-GAi; (2) fM-GAi drugs only display inhibitory activit