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1 racking the surface flow of apically applied microbeads).
2 plysia cell adhesion molecule (apCAM)-coated microbead.
3  Ndc80 complex, combined on the surface of a microbead.
4  many personal care products contain plastic microbeads.
5  gradient or with anti-TOM22-conjugated iron microbeads.
6 o form a hairpin structure and conjugated on microbeads.
7 tination of aptamer coated magnetic nano- or microbeads.
8 boflavin, amino acids and peptides from whey microbeads.
9 fic oligonucleotide probes bound to magnetic microbeads.
10 n or direct force application using magnetic microbeads.
11 gle-cell genomic DNA onto the coencapsulated microbeads.
12  not compromised by the low concentration of microbeads.
13 d by magnetic bead sorting via EPCAM labeled microbeads.
14 d in solution or immobilized on paramagnetic microbeads.
15  the flow path and holds ~300 5 mum-diameter microbeads.
16 s into multivalent complexes using protein A microbeads.
17 ices (cGMP)-grade anti-biotin immunomagnetic microbeads.
18 forces transmitted via spot-labeled magnetic microbeads.
19  trapping and mixing of solid-phase affinity microbeads.
20 cture for supporting antibody-functionalized microbeads.
21 polyacrylamide gel embedded with fluorescent microbeads.
22 D31)- and ICAM2 (also known as CD102)-coated microbeads.
23 tetramethylrhodamine, TMR) and attachment to microbeads.
24 ort, and detect individual superparamagnetic microbeads.
25  on resolving the trajectories of individual microbeads.
26 acrylamide substrates containing fluorescent microbeads.
27                              The immobilized microbeads (10-20 mum) are considerably larger than the
28   This paper focuses on encoding polystyrene microbeads, 10-100 microm in diameter, with a luminescen
29 ting process has been characterized by using microbeads (10microm diameter) resulting in a single bea
30 ed for single-cell analysis using Wnt-coated microbeads (12-18 h of live imaging) and to create a Wnt
31 ions of riboflavin were obtained in 'loaded' microbeads (361 mg/L) compared to riboflavin added to th
32 ents (ATL: 22.9%: MED: 14.7% PAC: 20.2%) and microbeads (4.8%; PAC only; to our knowledge the first i
33 FM probes with an attached N-cadherin-coated microbead (5 mum) induced a progressive clustering of N-
34                                     TentaGel microbeads (90 mum) were spatially segregated into outer
35                                     TentaGel microbeads (90 mum) were spatially segregated into outer
36                             As the volume of microbeads added to the solution was increased, the upta
37                                      Passive microbead affinity for WT and SPARC-null ECM did not dif
38                                          The microbeads allowed mapping of flow patterns and velociti
39 ric (FC) XM, and seven had DSA detectable by microbead analysis only.
40 nd reproducible functionalization of encoded microbeads and a high stability of DNA probes in cell-fr
41 e-coded mixture of multiple affinity-capture microbeads and an inertial microfluidic particle sorter
42 al tracking of collisions between insulating microbeads and an ultramicroelectrode surface are correl
43                            Using fluorescent microbeads and antihepsin treatment, we demonstrated tha
44  innate immunity by clearance of fluorescent microbeads and bacterial particles.
45 n and encapsulation of primer functionalized microbeads and cells.
46 el pad array units for the immobilization of microbeads and each gel pad array is surrounded with a P
47 tro in response to anti-CD3-anti-CD28-coated microbeads and IL-2.
48 intracameral injection of 35 mum polystyrene microbeads and measured common pathogenic outcomes in th
49 haracterizing the antibacterial copper-doped microbeads and monoliths (CuBs and CuMs), their antibact
50  The device was used to separate polystyrene microbeads and PC-3 human prostate cancer cells with 94.
51 ded in different density solutions, CsCl for microbeads and Percoll for cells.
52 ty) of previously well-characterized polymer microbeads and subsequently applied to determine the den
53 tly, the frequency of collisions between the microbeads and the electrode is not compromised by the l
54 e nature of the interactions between flowing microbeads and their influence on electrochemical proces
55 containing PDMS in the form of both precured microbeads and uncured liquid precursor, dispersed in wa
56 reptavidin-coated polyvinyltoluene (PVT) SPA microbeads and using [(125)I]IGF-1 as the endogenous lig
57        Finally, using anti-TCR-Vbeta8-coated microbeads and Vbeta8(-) Tregs, we show that TCR stimula
58 sition delivered approximately 16 times more microbeads and yielded approximately 20% more bacteria k
59  fluorescent microspheres, quantum dot-based microbeads, and fluorescent nano rods, some of which cur
60 rmed cylindrical plugs, preformed injectable microbeads, and hydrogel precursor, injected and polymer
61 eating with chemical lysis buffer and silica microbeads are employed for DNA extraction from clinical
62                                          The microbeads are fabricated by adsorbing fluoresceinamine
63                                     The PDMS microbeads are held together in thixotropic granular pas
64 c powder-containing enzyme-carrying alginate microbeads are immobilized on the surface of an electrol
65                        Fluorescently encoded microbeads are subsequently functionalized by lesion-con
66 gle-use polymer chip platform where magnetic microbeads are used as solid support to transport the DN
67                                    When whey microbeads are used as sorbents, they show excellent pot
68                                              Microbeads are used to track fluid flow over microband e
69                                         Whey microbeads are well suited to act as sorbents for encaps
70                                     Magnetic microbeads are widely used in biotechnology and biomedic
71 ngle cells, along with primer-functionalized microbeads, are randomly compartmentalized in the drople
72 ment of single human leukocyte antigen (HLA) microbead array assays allows characterization of host a
73 ol for common biolabs to customize their own microbead array for multi-analyte immunoassays.
74 development of more versatile and economical microbead array-based multiplex serological test panels
75  compared with that of a trapped polystyrene microbead as a function of the applied acoustic pressure
76 we describe the use of colloidal polystyrene microbeads as a sacrificial template to create a nanofib
77 ling circle amplification (RCA) and magnetic microbeads as a signal enhancement method.
78  improved by employing seven-element-encoded microbeads as a standard.
79 tical algorithm, which employs metal-encoded microbeads as an internal standard to correct the data f
80 oth PCV2 and PRRSV were used to validate the microbead assay (MBA) in comparison with the "gold stand
81 -specific antibody responses measured by the microbead assay were comparable to those of the standard
82 posttransplant DSA peaking at MFI >2000 U on microbead assay, rejection did not occur.
83 c antibody (DSA) level of more than 500 in a microbead assay.
84 tokines by immunohistochemistry, RT-PCR, and microbead assays.
85 lant, DSA levels were monitored closely with microbead assays.
86 uction of gold nanoparticles coated magnetic microbeads (Au NPs-MBs), which were prepared through a n
87 netics of blood flow recovery that resembled microbead-based blood flowmetry and laser Doppler blood
88 abeling sequences, and finally detected with microbead-based FFD assays.
89 infection status and a multiplex fluorescent microbead-based immunoassay and/or enzyme-linked immunoa
90 ere quantified using comprehensive multiplex microbead-based immunoassays for 46 immune mediators.
91 y chip for high-throughput and multi-analyte microbead-based immunoassays.
92  brain cells were measured simultaneously in microbead-based immunoassays.
93 ne mediators were quantified using multiplex microbead-based immunoassays.
94                       The approach employs a microbead-based protocol for the processes of affinity s
95 n-stained sputum smears were used to conduct microbead-based spoligotyping and assess genotypic resis
96 ust and inexpensive electrochemical magnetic microbeads-based biosensor (EMBIA) platform for PoC sero
97                                          The microbeads-based microfluidic platform is fully automate
98 ffects, and limited diffusion lengths in the microbead bed.
99 er cells with 94.7 and 1.2% of the cells and microbeads being deflected, respectively.
100 ectrophoresis, we used silica or polystyrene microbeads between 3-6 mum in diameter and packed them i
101                                       Silica microbead bioreactors (0.5 microm diameter) coated with
102  libraries are constructed on the surface of microbeads by ligating dsDNA fragments onto growing, sur
103 lavin loss, a second approach to 'load' whey microbeads by soaking in riboflavin was assessed.
104                                        These microbeads can be delivered in a minimally invasive mann
105 tte technique, spherical, glassified protein microbeads can be made that allow determination of prote
106 ranching networks in which superparamagnetic microbeads can be routed along dynamically-selected path
107          We propose that MAM7-functionalized microbeads can be used as a topical treatment, to reduce
108 dhesion inhibitors consisting of polystyrene microbeads chemically coupled to a protein known as mult
109 ed at controlled densities on the surface of microbeads coated with a phospholipid mixture resembling
110  assays and flow-based adhesion assays using microbeads coated with CEA immunopurified from LS174T co
111 FLA) onto carboxylate-functionalized polymer microbeads coated with poly(2-vinylpyridine) (PVP).
112 re identified in sera of healthy males using microbeads coated with recombinant denatured HLA-E or a
113                           In our experiment, microbeads coated with streptavidin were driven to the s
114                   Fluorescence images of the microbead column revealed captured bacteria as bright sp
115 sing manufacturer's recommended antibody and microbead concentrations produced inaccurate ALPL+ vs. A
116 evice, and a suspension of superparamagnetic microbeads conjugated to DNA molecules is introduced int
117 ule ends can be reconstituted in vitro using microbeads conjugated to the budding yeast kinetochore p
118                    Injections of fluorescent microbeads conjugated with a light-sensitive chromophore
119                                              Microbeads containing endothelial cells and stromal fibr
120                             Use of spiked-in microbead controls (e.g., AssayChex Process, Control Pan
121                      Furthermore, FST-loaded microbeads decreased bone ossification in developing chi
122 spray was able to deliver significantly more microbeads deeper in the biofilm compared with diffusion
123 d hydrogels were fully degraded within 2 wk; microbead degradation was more moderate, and plugs degra
124              These results indicate that the microbead device is a low-cost tool that enhances sample
125 n techniques, enzyme-based immunoassays, and microbead diagnostics.
126  acquired videos of single beating cells, of microbead displacement during contractions, and of fluor
127  microwells filled with ion-exchange polymer microbeads doped with various organic dyes.
128 ional element for selective antibody-coated, microbead-driven, large-scale expansion.
129 d with commercially available immunomagnetic microbeads (Dynabeads((R)) anti-Salmonella), polystyrene
130 used to prepare epoxide-functionalized glass microbeads (EGBs, 500 mum in size and manipulated by twe
131     For mice, a single 1-microL injection of microbeads elicited a highly regular 30% elevation in IO
132 hnique is first applied to match the pair of microbead embedded images before and after deformation,
133 o address this issue we prepared polystyrene microbeads encoded with seven elements (yttrium, indium,
134         A proof-of-concept superparamagnetic microbead-enzyme complex was integrated with microfluidi
135                                     Magnetic microbeads exhibit rapid separation characteristics and
136  rate of 2 muL/min, as characterized through microbead experiments, while maintaining measurement acc
137 than 24,000 images of 0.5 microm fluorescent microbeads flowing within mildly inflamed postcapillary
138 o create reaction geometries that confined a microbead flux to within 200 nm of the surface under flo
139 ve the outcome by using biodegradable fibrin microbeads (FMBs) to isolate a population of mesenchymal
140 ed by acoustic streaming (h >> lambdaf), the microbeads follow vortical streamlines in a pattern char
141 geometric separation of fluorescence-labeled microbeads for a multiplex detection in k levels.
142 , we describe the use of polyethylene glycol microbeads for the coincident delivery of EC and NSC as
143     Vessels deployed from these pre-cultured microbeads formed functional connections to host vascula
144 61 mg/L) compared to riboflavin added to the microbead forming solution (48 mg/L).
145                  Riboflavin was added to the microbead forming solution however diffusional losses of
146                            The United States Microbead-Free Waters Act was signed into law in Decembe
147 to drive the movement of analyte-bound glass microbeads from an aqueous sample into an immiscible hyd
148 nly; to our knowledge the first isolation of microbeads from marine megavertebrates).
149 se an anchoring molecule composed of agarose microbeads functionalized with an Fc-binding domain.
150 n <30 s using bead lane modules inside which microbeads functionalized with capture antibodies (cAbs)
151                              In this method, microbeads functionalized with multiple forward primers
152 e show that topical application of polymeric microbeads functionalized with the adhesin MAM7 to a bur
153 loped an in vitro actin assembly assay using microbeads functionalized with the nucleation promoting
154 arker) and anti-CD34 (EPC marker) conjugated-microbeads had the highest sensitivity and specificity f
155    RBCs were trapped directly (i.e., without microbead handles) in the dual optical tweezers where th
156 taneously pack multiple channels with silica microbeads having different sizes and surface properties
157                             On both RBCs and microbeads, human CD47 potently inhibits phagocytosis as
158 cking velocimetry (PTV) or by processing the microbead images by particle image velocimetry (PIV) sof
159 of four automated immunoassays (BioPlex 2200 microbead immunoassay [MBIA], Liaison chemiluminescence
160 scence immunoassay [CIA]); (2) Bioplex 2200 (microbead immunoassay); (3) fluorescent treponemal antib
161 mmunoassays, chemiluminescence immunoassays, microbead immunoassays) over another based on published
162  serum samples of H7N9 patients by multiplex-microbead immunoassays.
163 ed stored sera with HLA bound to polystyrene microbeads in a retrospective analysis of heart recipien
164       Velocities were determined by tracking microbeads in a solution containing electroactive potass
165 e microplastics, the bill banned all plastic microbeads in selected cosmetic products.
166 nts revealed fractionation of nanobeads from microbeads in the optimized device with high sorting eff
167 y to image cultured cells and membrane-bound microbeads in twelve independently-focusing channels sim
168 or cells together with primer functionalized microbeads in uniform PCR mix droplets.
169 nzymatic mineralization occur on polystyrene microbeads in water-in-oil emulsions, yielding synthetic
170 ered and microencapsulated human stem cells (MicroBeads) in the mouse eye, and to study the impact of
171                  Estimates using fluorescent microbeads indicated approximately 7,000 C1C2-binding si
172        The authors used tonometry to measure microbead-induced IOP elevations.
173 he same mice appears to be normal based on a microbeads-induced glaucoma model.
174 onducted within previous continuum models of microbead infiltration into tumour spheroids as they rel
175                                              Microbead-injected eyes showed reduced optokinetic track
176                                      Using a microbead injection technique to chronically raise IOP f
177      The AC loss began 4 weeks after initial microbead injection, corresponding to the time course of
178 iltering, this method discriminates the used microbeads into k levels and thereby introduces a geomet
179 ted unilaterally by injection of polystyrene microbeads into the anterior chamber to occlude aqueous
180 the final protein concentration of the solid microbead is controlled, and ranges from 700 to 1150 mg/
181                     Light focusing through a microbead leads to the formation of a photonic nanojet f
182 r transplantation, in 8 of 10 cases when the microbead level of DSA had median fluorescence intensity
183 dissociated hippocampal neurons we show that microbeads loaded with CASPR2, but not with a deletion m
184                                         Whey microbeads manufactured using a cold-set gelation proces
185 gen evolution reaction and superparamagnetic microbeads (MBs) as pre-concentration/purification platf
186  horseradish peroxidase (HRP)] onto magnetic microbeads (MBs) used as solid supports and amperometric
187 rsible capacity than conventional mesocarbon microbead (MCMB) powder.
188 lithiation of surface-fluorinated mesocarbon microbeads (MCMB-F) anodes.
189 sing ion selectivity of hydrogel-infiltrated microbead membranes.
190 ntibody (TPA) levels were measured using the microbead method in 44 presensitized patients who had re
191 intensity (MFI) >2000 U, in 6 of 10 when the microbead MFI >4000 U.
192                        In 8 of 10 cases, the microbead MFI at the time of resolution was greater than
193  Here we demonstrate for the first time that microbeads (microBs) can be used as contrast agents to t
194 he detection of single molecules in magnetic microbead microwell array formats revolutionized the dev
195  likely be reduced by further optimizing the microbead mixing.
196 s (MNBs); (2) optical imaging using magnetic microbeads (MMBs).
197 to 2 weeks of IOP elevation generated by the microbead model.
198 s has mainly been characterized by following microbead motion by optical microscopy either by particl
199 e use of neutravidin-functionalized magnetic microbeads (NA-MBs) modified with a biotinylated-anti-ds
200                                        Thus, microbead occlusion in a non-human primate with a visual
201 ibitor BIRB 796 in three models of glaucoma (microbead occlusion in rat and squirrel monkey and the g
202 tion and slows degeneration in the inducible microbead occlusion model of glaucoma in rat.
203                          Here we applied the microbead occlusion model of glaucoma to different trans
204 elevating the intraocular pressure (IOP) via microbead occlusion of ocular fluid outflow in mice.
205  week period of elevated pressure induced by microbead occlusion of ocular fluid, Trpv1(-/-) accelera
206 phic imaging performance is quantified using microbeads of different dimensions, as well as by imagin
207 ed 3D fabrication techniques we integrated a microbead on an AFM cantilever thus realizing a system t
208 diffraction intensity and the density of the microbeads on the surface varied as a function of PDGF-B
209  cytometric XM, and 23 had DSA detectable by microbead only.
210 positive cases, and in two of seven (29%) of microbead-only cases at a median of 6.5 days after trans
211 d to covalently immobilize Wnt3a proteins on microbeads or a glass surface.
212 ge on ground beef, without using antibodies, microbeads or any other reagents, towards a preliminary
213 ls and mouse tumor cells were isolated using microbeads or flow cytometry and analyzed for sphere-for
214 contrary, phagocytosis of solid polyethylene microbeads or treatment with soluble clofazimine rendere
215 on of collisions between individual magnetic microbeads, present at subattomolar concentrations, and
216 using a magnetic field to preconcentrate the microbeads prior to detection in a microfluidic electroc
217 rgeted) and 7.32 um (untargeted) polystyrene microbeads produced 18-fold higher permeate concentratio
218          Microencapsulated human stem cells (MicroBeads) promise to overcome limitations inherent wit
219                               Therefore, the Microbead Quantum-dots Detection System (MQDS) was devel
220              For rats, a single injection of microbeads raised IOP by 21% to 34%, depending on volume
221 netic separation process with antibody-bound microbeads, rapid and complete separation of specific ta
222  GFP-marked cells encapsulated in subretinal MicroBeads remained viable over a period of up to 4 mont
223 ECL signal, generated by thousands of carbon microbeads remotely addressed via bipolar electrochemist
224 ported in vivo VEGF release profile from the microbeads resulted in highly vascularized s.c. tissue c
225                                The 3% pectin microbeads resulted the best compromise between spherici
226                  CD15 cells were depleted by microbead separation.
227 o form a narrow channel with the polystyrene microbeads serving as spacers.
228  permeability measurements using fluorescent microbeads show that high-risk mucus was more permeable
229                           After 52weeks, the microbeads showed a total-astaxanthin retention of 94.1+
230 0 microg/ml) +/- CHC and unmodified alginate microbeads showed low responses.
231                                     Cellular microbeads showed vascularization potential comparable t
232           Moreover, by using spatial encoded microbeads, simultaneous detection of both hCG and PSA o
233 rogeneous phase by immobilization on polymer microbead solid supports.
234 ssay evaluating C3d deposition on HLA-coated microbeads spiked with alloantibodies.
235 ugh hybridization onto streptavidin-magnetic microbeads (Strep-MBs) modified with a complementary DNA
236 plete evaporation, we infiltrated the porous microbead structure with a positively or negatively char
237 advantageous characteristics of pre-cultured microbeads, such as volume preservation and vascular net
238 ly of different tag combinations onto SiO(2) microbead supports via biotin-avidin binding.
239 and sensitive quantification of aldehydes on microbead surfaces.
240 magnetic field acting on a superparamagnetic microbead suspended in an active medium.
241 sentation of engineered cell-secreted ECM on microbeads suspended in alginate hydrogels would promote
242            RSI was validated using a plastic microbead suspension (poly(methyl methacrylate) (5-27 mu
243      25 cytokines were measured by multiplex microbead system (Invitrogen, UK) on a Luminex platform.
244                   To test this hypothesis, a microbead system was utilized to measure relative L-sele
245         Here, we developed cell-laden fibrin microbeads that can be pre-cultured to form primitive va
246 ynthesis conditions were optimized to obtain microbeads that were uniform in size and generated stron
247        When either fragment was coupled to a microbead, the force it could transduce from a shortenin
248 uidic channels with silica nanoparticles and microbeads, thereby indirectly producing functional nano
249 the density and compressibility of cells and microbeads; these being the two central material propert
250 noparticles (SPIONs) with mesoporous CaCO(3) microbeads to a magneto-fluorescent bead platform that c
251 mplemented with ssDNA aptamer functionalized microbeads to address the specific capturing of thrombin
252  covalently immobilised on superparamagnetic microbeads to allow the isolation of BBI from soy whey m
253 valuate the strategy of using self-assembled microbeads to build a robust and tunable membrane for fr
254  this efficiently, stLFR uses the surface of microbeads to create millions of miniaturized barcoding
255 ned by replacing the bacteria by polystyrene microbeads to demonstrate the internalization of the lig
256 video microscopy, we tracked selectin-coated microbeads to detect the formation frequency of adhesive
257 ion of DNA-based fluorescent chemosensors on microbeads to differentiate eight toxic metal ions in wa
258  (digital diffraction diagnosis) system uses microbeads to generate unique diffraction patterns which
259                  Finally, utilizing magnetic microbeads to mechanically stimulate mechanically-inhibi
260 al techniques rely on nanometric tracking of microbeads to obtain quantitative information about the
261 ere, we report the utilization of dielectric microbeads to significantly enhance the photon upconvers
262 latter recombinant protein could also couple microbeads to the ends of shortening microtubules and us
263 vection from the spheroid surface, by adding microbeads to the surface of tumour spheroids and observ
264 s of microscale particles, such as cells and microbeads, to biofunctional surfaces is difficult becau
265                                              Microbead trajectories show a systematic deviation towar
266                     The dynamics of magnetic microbead transport by domain walls has been well studie
267  of a depolymerizing MT and can couple it to microbead transport in vitro.
268       It consists of monomeric avidin-coated microbeads trapped in a pipette tip and has been used fo
269              The fluidic system used a novel microbead-trapping flow cell to capture antibody-coupled
270                        Detection of a single microbead was successfully demonstrated using a capacita
271 -the-spot packing of antibody-functionalized microbeads was completed in <20 s followed by autonomous
272  peptides of varying hydrophobicities by the microbeads was examined.
273 ch the binding to rhSHBG-coated paramagnetic microbeads was inhibited by any other binding (designer)
274                     Intraocular injection of microbeads was made in mouse eyes to elevate intraocular
275                     Riboflavin uptake by the microbeads was shown to be via a partition process.
276                   Long-term stability of the microbeads was studied for 6 months taking into account
277 grade tracer, red (RFB) or green (GFB) latex microbeads, was injected into the gustatory PBN under el
278 tributions of noninteracting and interacting microbeads, we observed that tether bond formation rates
279 dingly, 1 mum half-gold and half-fluorescent microbeads were conjugated with 200 nm nanobeads through
280        Fluorescent E. coli bound to magnetic microbeads were driven through the microfluidic device u
281 ed for Thy-1 expression using immunomagnetic microbeads were enriched from 5.2%-87.2% Thy-1(+).
282  only in the grease that the much publicised microbeads were found.
283                                              MicroBeads were implanted into the subretinal space of S
284 r scale by passive microrheology techniques: microbeads were injected in jellyfish ECM and their Brow
285 esia, up to 2 muL of fluorescent or magnetic microbeads were injected intracamerally into the mouse e
286  green (GFB) and red (RFB) fluorescent latex microbeads were injected iontophoretically or by pressur
287                                   Blank whey microbeads were placed in solutions of the compounds.
288                                        While microbeads were present in the host sediment matrix, the
289                           In this study whey microbeads were used to encapsulate riboflavin using 2 m
290  multi-use immunosensor, disposable magnetic microbeads were used to immobilize biomarker-recognition
291 of the resolution enhancement induced by the microbead, which sheds light into the many contradictory
292  amplification factor of 250000 and magnetic microbeads, which are mobile solid-phase supports for th
293 ARC-null mice were injected with fluorescent microbeads, which were also passively exposed to freshly
294                                              Microbeads with a diameter of 20 mum are first functiona
295               We demonstrate manipulation of microbeads with diameters from 1.5 to 10 um and Jurkat c
296 d particles were performed using polystyrene microbeads with different sizes to demonstrate rapid (<1
297 fficiently trap a large number of individual microbeads with enriched exosomes at the single-particle
298 thelial progenitor cells (EPCs) by combining microbeads with fluorescence quantum dots (Q-dots) coupl
299 approach was used to obtain calcium-alginate microbeads with high polyphenol content and good morphol
300                               Porous agarose microbeads, with high surface to volume ratios and high
301 he microfluidic chip contained packed silica microbeads zones to filter and enrich the norovirus infe

 
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