ライフサイエンスコーパス: SRM

1 SRM 1950 is the first reference material developed speci

2 SRM 1950 Metabolites in Human Plasma is intended to have

3 SRM 612 (Trace Elements in Glass) was also analyzed desp

4 SRM 972a was developed in collaboration with the Nationa

5 SRM detection provides the relative quantitation of each

6 SRM domains are then polarized by the microtubule-depend

7 SRM polarization requires F-actin but not the F-actin or

8 al certified reference materials (SRM 1568a, SRM 1570a, CRM 7503-a, BC211 and IPE-120) were analysed

9 ients undergoing active surveillance for 957 SRMs indicates that the majority grew during observation

10 The ABHD5/SRM/spermidine axis in TAMs might represent a potential

11 ns below 1500 Hz, are critical for achieving SRM in NH listeners.

12 th in mice can be prevented by an additional SRM transgene in macrophages.

13 hese methods, biologists have begun adopting SRM to address a wide range of questions in many types o

14 ation outcome was best predicted by advanced SRM stage (hazard ratio, 4.89; P<0.0001) and diabetes me

15 thione are also moderately selective against SRM.

16 promises that must be made when designing an SRM experiment.

17 ing risks of mortality, all patients with an SRM should be considered for a biopsy when the results m

18 electrophoresis than nephelometric data and SRM is unaffected by antigen excess.

19 groundwater, NIST SRM 1568b Rice Flour, and SRM 1632 bituminous coal.

20 Hg and Pb in NIST SRM 1547 peach leaves and SRM 1573a tomato leaves reference materials and three he

21 eference materials SRM 1547 Peach Leaves and SRM 1573a Tomato Leaves.

22 dard reference materials (BCR-482 Licken and SRM 1573a Tomato Leaves) and spiked real food and herb s

23 st, SRM 1650b Diesel Particulate Matter, and SRM 2975 Diesel Particulate Matter (Industrial Forklift)

24 We approach SRM from another direction: we focus on the current prac

25 Atrial SRM is identified on LGE-MRI, and extensive LGE (>/=30%

26 accessory olfactory bulb stimulation before SRM acquisition blocked long-term SRM, supporting the in

27 Patients were categorized by SRM stage (I-IV) based on the percentage of LA wall enha

28 quential analysis of fractionated eluates by SRM (SAFE-SRM), to plasma from cancer patients and disco

29 ent of these proteins in nuclear extracts by SRM permitted the reproducible quantification of 42% of

30 amples were digested by trypsin, followed by SRM detection.

31 with up to three charges, can be targeted by SRM on a triple quadrupole instrument.

32 s Proteotypic Predictor, to select candidate SRM transitions when no previous mass spectrometry evide

33 proteome and its use in selecting candidate SRM peptides to establish assays for use in determining

34 ltiplexing before nano-liquid chromatography-SRM quantification.

35 areas of almost 90% compared to conventional SRM.

36 enges are addressed to effectively correlate SRM with other microscopy techniques, including light mi

37 also discuss the application of correlative SRM to materials characterization and single-molecule re

38 Application of DD-SRM to human serum and tissue provides precise quantific

39 ed an antibody-independent deep-dive SRM (DD-SRM) approach that capitalizes on multidimensional high-

40 Thus, DD-SRM holds great promise for precisely measuring extremel

41 tein level were observed when comparing DDA, SRM and LA-ICP-MS results.

42 While the goal of well-designed SRM methods is to monitor for unique precursor-product i

43 peptides coupled to stable isotope dilution-SRM (SID-SRM).

44 Dimethyl-SRM was further examined by comparing the relative quant

45 eveals that the correlation between dimethyl-SRM and SID-SRM is within 0.3-33% variation, demonstrati

46 with selected reaction monitoring (dimethyl-SRM).

47 racy of relative quantitation using dimethyl-SRM.

48 developed an antibody-independent deep-dive SRM (DD-SRM) approach that capitalizes on multidimension

49 asurements of diagnostic product ions during SRM transitions by ratiometric comparisons with stable i

50 an Particulate Matter, SRM 1649b Urban Dust, SRM 1650b Diesel Particulate Matter, and SRM 2975 Diesel

51 m was employed and cross-validated by LC-ESI-SRM-MS/MS.

52 ssociation-selected reaction monitoring (ETD-SRM) was developed to investigate isoAsp sites in MUPs.

53 to selected reaction monitoring experiments (SRM) as it may result in a gain in selectivity in detect

54 fort highlights the development of the first SRM for reduced nicotine and reduced tobacco-specific ni

55 For SRM 2975, large increases (>100%) are also observed for

56 For SRM inhibition, MFP is synergistic with nitrite and chlo

57 tions, composting may be a viable method for SRM disposal.

58 e that experimental conditions optimized for SRM 955c (caprine blood) are not valid for human blood s

59 of establishing precursor-product pairs for SRM.

60 Selecting the best peptides for SRM analysis to ensure that protein- or gene-specific in

61 s in Frozen Human Serum as a replacement for SRM 972, which is no longer available.

62 ple is more than 3 times lower than that for SRM 955c.

63 Radical nephrectomy for SRMs should only be reserved for patients who possess a

64 Partial nephrectomy (PN) for SRMs is the standard treatment that should be offered to

65 This novel 3D fluorescence-free SRM technique was successfully applied to resolve the po

66 presents the first of its kind for a gaseous SRM developed by NIST.

67 ncertainties specified to date for a gaseous SRM produced by NIST.

68 ensitivity obtained from ablation of a glass SRM.

69 n of the crater size when ablating the glass SRM.

70 r the highly selected reaction monitoring (H-SRM) mode, the detection limit of O(2)-edT, N(3)-edT, an

71 thmias (failed ablations) occurred at higher SRM stages with 28 of 133 (21.0%) in stage I, 40 of 140

72 The linear range of HILIC-SRM was slightly less ( approximately 3 orders of magnit

73 The performance was compared with two IA SRM methods which were recently validated for individual

74 ndard selected reaction monitoring assay (ID-SRM).

75 ved to be equivalent to the gold-standard ID-SRM in terms of sensitivity (1-10 ppm), accuracy, and pr

76 ate within a factor of 2 when compared to ID-SRM.

77 Despite its importance, SRM is still relatively little studied.

78 actions of interest, significantly improving SRM sensitivity by approximately 5 orders of magnitude w

79 As in SRM, quantification using DIA data is based on the area

80 Averaged measurements of FA and 5-MTHF in SRM-1849a were within the certified value range.

81 ologists navigate through common pitfalls in SRM specimen preparation and optimization of image acqui

82 ecently we have made significant progress in SRM sensitivity for enabling quantification of low nanog

83 and conventional liquid chromatography (LC)-SRM (45 min gradient) showed that the long-gradient sepa

84 r multiplexing capacity than conventional LC-SRM due to an increase in average peak widths (~3-fold)

85 f magnitude when compared to conventional LC-SRM.

86 The immuno-LC-SRM assay has a limit of detection of 2 x 10(4) CFU/mL i

87 omatography selected reaction monitoring (LC-SRM) analyses of low-abundance peptides spiked into a hi

88 omatography-selected reaction monitoring (LC-SRM) approach that we demonstrate is capable of quantita

89 While the performance of LC-SRM applied to samples from various bodily fluids, parti

90 Due to these properties, LC-SRM has the potential to become the foundation for bioma

91 metry using selected reaction monitoring (LC/SRM-MS) holds great promise for targeted protein analysi

92 efficient strategy to develop an optimal LC/SRM-MS method.

93 oupled with selected reaction monitoring (LG-SRM) for targeted protein quantification.

94 Direct comparison of LG-SRM (5 h gradient) and conventional liquid chromatograph

95 of >0.99 was observed for the results of LG-SRM and enzyme-linked immunosorbent assay (ELISA) measur

96 Further enhancement of LG-SRM sensitivity was achieved by applying front-end IgY14

97 Besides improved sensitivity, LG-SRM potentially offers much higher multiplexing capacity

98 The LG-SRM detection of seven out of eight endogenous plasma pr

99 Therefore, LG-SRM holds great potential for bridging the gap between g

100 nt selection of target fractions via on-line SRM monitoring of internal standards, and fraction multi

101 st that the proposed oxygen and LLL12 loaded SRMs provide a promising drug delivery strategy for more

102 which hurdles still need to be taken to make SRM a robust and more accurate method for sFLC measureme

103 vide a basis for solar radiation management (SRM) geoengineering.

104 Spatial release from masking (SRM) occurs when spatial separation between a signal and

105 ffect known as spatial release from masking (SRM).

106 PURPOSE OF REVIEW: Small renal masses (SRMs) are frequently encountered due to the ubiquitous u

107 : Management options for small renal masses (SRMs) include excision, ablation, and active surveillanc

108 ptions for patients with small renal masses (SRMs).

109 y analysing the standard reference material (SRM 1577 b).

110 y analyzing the standard reference material (SRM 1640a) and spiked real samples.

111 ST) new protein standard reference material (SRM 8671) is becoming the benchmark molecule against whi

112 a bovine blood standard reference material (SRM 966, Level 2).

113 Standard Reference Material (SRM) 1649b Urban Dust was characterized; 34 organic acid

114 constitute NIST Standard Reference Material (SRM) 1720 Northern Continental Air, were certified by NI

115 and Technology Standard Reference Material (SRM) 1950, "Metabolites in Frozen Human Plasma", against

116 total sulfur in Standard Reference Material (SRM) 2682c Subbituminous Coal (nominal mass fraction 0.5

117 ) has developed Standard Reference Material (SRM) 972a Vitamin D Metabolites in Frozen Human Serum as

118 tion of a glass standard reference material (SRM) and the Al layer as reference, the deviations betwe

119 tobacco filler Standard Reference Material (SRM) has been issued by the National Institute of Standa

120 has developed a Standard Reference Material (SRM) to support technology development in metabolomics r

121 s in house dust standard reference material (SRM).

122 in a house dust standard reference material, SRM 2585, demonstrating their environmental relevance.

123 and Pb in NIST standard reference materials SRM 1547 Peach Leaves and SRM 1573a Tomato Leaves.

124 alidated using certified reference materials SRM 1570A (spinach leaves) with satisfactory and compati

125 Several certified reference materials (SRM 1568a, SRM 1570a, CRM 7503-a, BC211 and IPE-120) wer

126 NIST Standard Reference Materials (SRM) 3257 Catechin Calibration Solutions and 3255 Camell

127 omium from the standard reference materials (SRM) candidate NIST 2700 and NIST 2701.

128 ns of disposing of specified risk materials (SRM) or animal mortalities potentially infected with pri

129 dry whole air standard reference materials (SRMs 1720 and 1721) and the NIST Traceable Reference Mat

130 four powdered standard reference materials (SRMs) fused in lithium borate glasses: two sediments as

131 pheres as NIST standard reference materials (SRMs).

132 udy were SRM 1648a Urban Particulate Matter, SRM 1649b Urban Dust, SRM 1650b Diesel Particulate Matte

133 , randomly distributed sterol-rich membrane (SRM) domains form at the plasma membrane, independent of

134 bute to long-term social recognition memory (SRM) formation.

135 Social recognition memory (SRM) is crucial for reproduction, forming social groups,

136 hought to mediate social recognition memory (SRM).

137 d LLL12 in stimuli responsive microdroplets (SRMs) by a gas-driven coaxial flow focusing (CFF) proces

138 reservoirs, sulfate reducing microorganisms (SRM) produce hydrogen sulfide which is toxic, explosive,

139 respiratory sulfate reducing microorganisms (SRM), and no study has systematically and quantitatively

140 cal Raman spectroscopy (SRS) and microscopy (SRM).

141 of super-resolution fluorescence microscopy (SRM) opened an unprecedented vista into nanoscopic lengt

142 y using optical super-resolution microscopy (SRM) and combinatorial labeling.

143 Final, 3D super-resolution microscopy (SRM) images were obtained by resolving 3D coordinates an

144 The rise of super-resolution microscopy (SRM) over the past decade has drastically improved the r

145 he field of superresolution (SR) microscopy (SRM).

146 Selected reaction monitoring mode (SRM) of tandem mass spectrometry was developed for analy

147 for the sulfate reduction pathway in a model SRM, we screened a panel of inorganic oxyanions.

148 used the fugacity-based small-region model (SRM) to calculate predicted environmental concentrations

149 This novel spectral resonance modulator (SRM) shows great potential in an ultrafast compressive s

150 s method using selected reaction monitoring (SRM) aimed at quantitative profiling of the stoichiometr

151 MS assay using selected reaction monitoring (SRM) allows simultaneous quantitation of five molecular

152 SI MS/MS) with selected reaction monitoring (SRM) and quantitation by high mass accuracy analysis of

153 oduce a set of selected reaction monitoring (SRM) assays for the systematic measurement of 464 protei

154 ion (HRMS) and selected reaction monitoring (SRM) based mass spectrometric detection to quantify a po

155 rsor ions for selective reaction monitoring (SRM) detection.

156 ort the use of selected reaction monitoring (SRM) for tracking proteolysis induced by human apoptotic

157 time-triggered selected reaction monitoring (SRM) in positive electrospray ionization (ESI) mode.

158 methylation by selected reaction monitoring (SRM) is one of the current quantitative methods.

159 5, and PLF4 by selected reaction monitoring (SRM) liquid chromatography (LC)-MS/MS.

160 that utilizing selected reaction monitoring (SRM) mass spectrometry allows researchers to confirm pro

161 f principle, a selected reaction monitoring (SRM) mass spectrometry-based methodology was applied to

162 AC approach to selected reaction monitoring (SRM) mass spectrometry.

163 ometry (MS) in Selected Reaction Monitoring (SRM) mode is proposed for in-depth characterisation of m

164 re detected in selected reaction monitoring (SRM) mode, and transition m/z 874.3 --> 778.3 was used f

165 roid esters in selected reaction monitoring (SRM) mode, for the first time in ASAP.

166 d MS using the selected reaction monitoring (SRM) mode.

167 (SIM) mode and selected reaction monitoring (SRM) mode.

168 n SPROX using selective reaction monitoring (SRM) on a triple quadrupole mass spectrometer (QQQ-MS).

169 he upcoming LC-selected reaction monitoring (SRM) technique which combines high technical accuracy wi

170 erences in the selected reaction monitoring (SRM) transition of the signature peptide due to the incr

171 ing different selective reaction monitoring (SRM) transitions or adding more labeling positions.

172 Similarly to selected reaction monitoring (SRM), peptides can be quantified from DIA data using tar

173 is the use of selected reaction monitoring (SRM), where the areas under the curve (AUCs) of peptides

174 performed by selective reaction monitoring (SRM), while the presence of a product ion at m/z 355, sp

175 ere describe a selected reaction monitoring (SRM)-based approach for the discovery and validation of

176 We applied selected reaction monitoring (SRM)-based proteomics, profiling 43 proteins in serum pr

177 rt an extended selected reaction monitoring (SRM)-based strategy to reproducibly and quantitatively m

178 tion (DDA) and selected reaction monitoring (SRM).

179 uantitation by selected reaction monitoring (SRM).

180 as achieved by selected reaction monitoring (SRM).

181 termination by selected reaction monitoring (SRM).

182 teomics (e.g., selected reaction monitoring, SRM) is emerging as an attractive alternative to immunoa

183 ometric method selected reaction monitoring, SRM.

184 on state within its Slimb-recognition motif (SRM).

185 A novel LC/MS/MS SRM-based method has been developed to detect and quanti

186 l protein identification technology (MudPIT)-SRM, taking advantage of the robust online strong cation

187 Applying the MudPIT-SRM approach to profile abundant plasma proteins, we dem

188 The MudPIT-SRM method is relatively facile to conduct and offers pe

189 NIST SRM 1515 Apple leaves and GBW-07605 Tea certified refere

190 ce materials (SLRS-4 Riverine water and NIST SRM 1515 Apple leaves).

191 sis of LGC 6010 Hard drinking water and NIST SRM 1573a Tomato leaves standard reference materials.

192 rformance using pooled human plasma and NIST SRM 1950 samples.

193 and improving extraction of Cr(VI) from NIST SRM 2701, a standard COPR-contaminated soil.

194 -611) low level bromide in groundwater, NIST SRM 1568b Rice Flour, and SRM 1632 bituminous coal.

195 e determination of As, Cd, Hg and Pb in NIST SRM 1547 peach leaves and SRM 1573a tomato leaves refere

196 s of the APC and the reference material NIST SRM 1632d were compared to data in the literature.

197 ternational standard reference material NIST SRM 977 (delta(81)BrSMOB = -0.65 +/- 1.1 per thousand, 1

198 rice flour standard reference material (NIST SRM 1568a).

199 d using a certified reference material (NIST SRM 1643e) and groundwater sample analysis, indicating t

200 Technology Standard Reference Material (NIST SRM) 2779 Gulf of Mexico crude oil by GC coupled to vacu

201 lyses of certified reference materials (NIST SRM 1515 Apple leaves, IAEA 336 Lichen, GBW 07605 Tea).

202 nalysing certified reference materials; NIST SRM 1515 Apple leaves, IAEA-336 Lichen and GBW-07605 Tea

203 o that of the bone mineral component of NIST SRM 1486 (bone meal), as determined by powder X-ray diff

204 h a QTA, as demonstrated by analysis of NIST SRM 1643e (trace elements in water).

205 , we have performed global profiling of NIST SRM 1950, "Metabolites in Human Plasma", using GC-MS, LC

206 the certified values in the analysis of NIST SRM 955c (Caprine Blood) Level 3 and the certified human

207 he assay for standard reference plasma (NIST SRM 1950) were 107% and 6.7%, respectively.

208 ully applied to different food samples (NIST SRM 2976 mussel tissue, pepper, ginger, wheat flour, red

209 ne Premium Coal (APC) series and in the NIST SRM 1632d is presented.

210 5)Tl/(203)Tl ratio of a sample from the NIST SRM 997 Tl isotope standard in parts per 10(4)) versus 1

211 identical within experimental errors to NIST SRM 2779, demonstrating that Marlin crude is an appropri

212 n a certified reference material, viz., NIST SRM 1640a natural water, which was found to be in good a

213 species concentrations for levels 2 and 4 of SRM 955c are reported here for the first time.

214 roposed method was evaluated by analysing of SRM Apple Leaves 1515 certified reference material.

215 y of the method was evaluated by analysis of SRM 1573a with good agreement compared to the certified

216 e method was investigated by the analysis of SRM and the recovery of analytes from various spiked foo

217 the multiplexed, quantitative attributes of SRM.

218 ts of mass spectrometers that are capable of SRM.

219 er, play major roles in the consolidation of SRM, but these roles are different in each structure vis

220 s in both structures in the consolidation of SRM.

221 To test the effectiveness of SRM mass spectrometry in determining protein abundance i

222 w opportunities in the fast-growing field of SRM.

223 MFP remains a potent inhibitor of SRM growing by fermentation, and MFP is tolerated by nit

224 identify potent and selective inhibitors of SRM, quantitatively ranked the selectivity and potency o

225 erence material, three of the four levels of SRM 972a are composed of unmodified human serum.

226 ely evaluated the selectivity and potency of SRM inhibitors.

227 The plasma used in the preparation of SRM 1950 was collected from both male and female donors,

228 of reviews on the fundamental principles of SRM and the remarkable achievements made with these meth

229 s that may compromise the reproducibility of SRM data.

230 irectional hearing, but the possible role of SRM, or whether such specializations exhibit limitations

231 Here we expand the scope of SRM to photoactivated localization microscopy (PALM) ima

232 These results demonstrate the utility of SRM-based targeted proteomics to guide the identificatio

233 Histological validation of SRM was performed comparing LGE-MRI with surgical biopsy

234 Extirpative treatment of SRMs may be associated with worse outcomes, particularly

235 odified from those utilized for the previous SRM, and all three approaches now incorporate chromatogr

236 The PRISM-SRM quantification of protein phosphorylation illustrate

237 rate that the CFF process is able to produce SRMs with uniform size distribution, large oxygen loadin

238 left atrial (LA) wall structural remodeling (SRM) and stratify patients who are likely or not to bene

239 nalysis of fractionated eluates by SRM (SAFE-SRM), to plasma from cancer patients and discovered two

240 ved for the other diesel particulate sample, SRM 1650b.

241 rtified Reference Materials (marine sediment SRM 1944, fish tissue 1947, and loamy soil CRM 962-50) a

242 MFP) was not known previously as a selective SRM inhibitor, but has promising characteristics includi

243 caused by the digestion and a less selective SRM transition of the signature peptide as compared to u

244 s) in the standard reference material serum (SRM 1958, NIST).

245 We identified several SRM selective inhibitors including selenate, selenite, t

246 In samples with high levels of sFLC, SRM data was more consistent with serum protein electrop

247 the correlation between dimethyl-SRM and SID-SRM is within 0.3-33% variation, demonstrating the accur

248 coupled to stable isotope dilution-SRM (SID-SRM).

249 Furthermore, a single SRM method may include simultaneous monitoring of tens t

250 use with UV and/or tandem mass spectrometry (SRM) detection.

251 ctive reaction monitoring-mass spectrometry (SRM-MS) is sufficiently sensitive to detect latent HIV r

252 ptimized and finally a sensitive streamlined SRM based analytical method for allergens detection in i

253 Potential implications for studying SRM in hearing-impaired listeners are discussed.

254 w that the lipolytic factor ABHD5 suppresses SRM-dependent spermidine production in TAMs and potentia

255 cally, ABHD5 suppresses spermidine synthase (SRM)-dependent spermidine production in macrophages by i

256 we present can be readily adapted to target SRM in diverse environments and similar strategies could

257 lly detected and quantified using a targeted SRM workflow.

258 e mice impaired the persistence of long-term SRM but had no effect on sociability and preference for

259 on test to evaluate short-term and long-term SRM in adult Sprague-Dawley male rats (n = 38).

260 Our results indicate that long-term SRM in rats involves protein synthesis and oxytocin-depe

261 ion before SRM acquisition blocked long-term SRM, supporting the involvement of LTD in the MeA in for

262 ated rats, which are known to lack long-term SRM.

263 of LTD in the MeA in formation of long-term SRM.

264 the MeA prevented the formation of long-term SRM.

265 is crucial for the persistence of long-term SRM.SIGNIFICANCE STATEMENT Oxytocin receptors (OXTRs) ar

266 We demonstrate that SRM can be extended toward reproducible detection and qu

267 Together, these results indicate that SRM-MS is a viable method for measuring latent HIV-1 res

268 We show that SRM protein analysis is a sensitive and rapid approach t

269 We conclude that SRMs are key to cell polarization.

270 The SRM method only measured a signature peptide generated f

271 on to this trend was the loss of PsbO in the SRM analysis, which highlights the necessity of validati

272 Within 60-80 minutes, the SRM method performs microbial identification (I), antibi

273 ditions suggests that the performance of the SRM increases when worst-case conditions are replaced by

274 he approach by demonstrating that two of the SRM-identified factors, Mot3 and Azf1, are required for

275 ntermediate precision analyses show that the SRM 1950 profiling is reproducible enough to consider th

276 ng, the results presented here show that the SRM strategy developed for multibiomarker measurement pa

277 tion of a single residue (Ser293) within the SRM is critical for Slimb binding and ubiquitination.

278 n when extracted at 100 degrees C in all the SRMs studied.

279 This SRM application is illustrated by the analysis of the hu

280 This SRM has certified and reference values for the following

281 This SRM was designed to apply broadly to the field, not towa

282 Value assignment of this SRM was accomplished using a combination of three isotop

283 holds or improve localization accuracy, thus SRM does not operate in this range of spatial separation

284 First, the isotopic contribution to SRM (ICSRM) of the proposed SIL drug and SIL internal st

285 The specific contribution of the MeA to SRM formation and the specific actions of oxytocin in th

286 (ENV) and temporal fine structure (TFS), to SRM in normal-hearing (NH) human listeners.

287 y of PRM assays were compared to traditional SRM workflows on triple quadrupole instruments.

288 The measurement accuracy in two SRMs was 71-113%.

289 Unlike SRM, data acquisition is not constrained to a predetermi

290 ounds and identified previously unrecognized SRM selective inhibitors and synergistic interactions be

291 We further use SRM to visualize nm-thin yet mum-long dynamic, supramole

292 /z 404-->m/z 386) in positive ESI mode using SRM scanning.

293 th conventional lipidomic quantitation using SRM scans on a triple quadrupole (QqQ) mass analyzer, (2

294 cialization has lowered the barrier to using SRM and the awarding of the Nobel Prize has drawn attent

295 The four materials used in the study were SRM 1648a Urban Particulate Matter, SRM 1649b Urban Dust

296 ion of stable isotope labeling combined with SRM can overcome many of the current potential analytica

297 om surgical biopsy specimens correlated with SRM on LGE-MRI.

298 tion, we used 2D chromatography coupled with SRM of candidate peptides.

299 Dimethyl labeling coupled with SRM provides a fast, convenient, and cost-effective alte

300 sFLC concentrations measured with SRM were comparable to those obtained by nephelometry an