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1 ethods based on biological properties (e.g., immunoaffinity).
2 n 70 (HSP70) IgG was isolated from plasma by immunoaffinity.
3 GFR protein (CD271, p75NTR) were isolated by immunoaffinity adsorption, and cultured as a monolayer f
4 m complex biological samples, without use of immunoaffinity agents.
5                                           By immunoaffinity and enzyme-linked immunosorbent assay tec
6                                        Using immunoaffinity and high-performance liquid chromatograph
7                                        After immunoaffinity and HPLC purification, MALDI/MS measured
8 f patients with pancreatic cancer, including immunoaffinity and label-free physical attribute-based c
9     Using a variety of approaches, including immunoaffinity and mass spectrometry, we identified a pr
10 f >10 mg of monomeric hOR17-4 receptor after immunoaffinity and size exclusion chromatography, with e
11 eled CCR5, which was purified using a tandem immunoaffinity and size-exclusion chromatography approac
12       Macrophage exosomes and MV isolated by immunoaffinity and sucrose cushion centrifugation were c
13                                     Using an immunoaffinity approach followed by multipoint validatio
14  (hSPC25) and human SPC24 (hSPC24), using an immunoaffinity approach.
15                                              Immunoaffinity assays are the workhorse for measuring in
16 observations demonstrate the utility of CD45 immunoaffinity-based approaches for producing highly pur
17 rochannel and also a technique for improving immunoaffinity-based circulating tumor cell (CTC) captur
18                                              Immunoaffinity-based CTC isolation has also been employe
19 vice to integrate size-based separation with immunoaffinity-based CTC isolation.
20               In the work presented here, an immunoaffinity-based LC/MS/MS assay was developed and va
21                            The assay uses an immunoaffinity-based liquid chromatography-tandem mass s
22 that is a simple and reliable alternative to immunoaffinity-based methods.
23 c monoclonal antibodies and therefore, allow immunoaffinity-based purification.
24 as isolated through binding of either tag to immunoaffinity beads and then decorated with antibodies
25 use in surface plasmon resonance (SPR)-based immunoaffinity biosensors.
26  cow's milk allergy has been performed using immunoaffinity capillary electrophoresis (IACE) coupled
27          We utilized a novel microchip-based immunoaffinity capillary electrophoresis technology to m
28                                              Immunoaffinity capture and mass spectrometry revealed as
29 say that uses sequential protein and peptide immunoaffinity capture for protein target quantitation.
30                            We established an immunoaffinity capture LC-HRMS method to quantify the in
31                 The protocol starts with the immunoaffinity capture of naturally processed MHC-peptid
32 nd AhR knockdown H358 cells was validated by immunoaffinity capture stable isotope dilution ([(15)N(5
33 on density gradient fractionation and direct immunoaffinity capture to precisely characterize the RNA
34 t-generation disulfide-linked ADCs involving immunoaffinity capture, chemical cleavage, and LC-MS/MS.
35                                    Following immunoaffinity chromatographic purification from rat liv
36                                              Immunoaffinity chromatography (IAC) was used to isolate
37 V detection, after prior matrix isolation by immunoaffinity chromatography (IAC).
38 fied ISGylated proteins from human thymus by immunoaffinity chromatography and analyzed ISG15 conjuga
39 ctrometry (MS/MS) assay that utilizes online immunoaffinity chromatography and column switching was d
40 , we isolated apo(a)-containing particles by immunoaffinity chromatography and determined the concent
41 ted complexes containing PLTP from plasma by immunoaffinity chromatography and determined their compo
42                           We performed ATP7A immunoaffinity chromatography and identified 541 protein
43 he intervention measured by using sequential immunoaffinity chromatography and liquid chromatography-
44                       Using a combination of immunoaffinity chromatography and mass spectrometry, we
45 f serpin-6 and PAP-3 in induced hemolymph by immunoaffinity chromatography and mass spectrometry.
46                                      We used immunoaffinity chromatography and mass spectroscopy to i
47 s were analyzed with mass spectrometry after immunoaffinity chromatography and peptide elution.
48 300 gel filtration chromatography, anti-FLAG immunoaffinity chromatography and SDS/PAGE permitted pur
49                                        Using immunoaffinity chromatography and tandem mass spectromet
50 zed receptor was easily purified by one-step immunoaffinity chromatography and the purified receptor
51      In this study, we applied an integrated immunoaffinity chromatography and top-down MS approach t
52  as separated by anti-apoC-III and anti-apoE immunoaffinity chromatography and ultracentrifugation in
53 d several mutants, from transfected cells by immunoaffinity chromatography and visualized individual
54 say methods were developed for detection and immunoaffinity chromatography capture was developed for
55      PAP-serpin-3 complexes were isolated by immunoaffinity chromatography from hemolymph activated b
56 C heterocomplex was isolated and purified by immunoaffinity chromatography from insect cells co-expre
57 is mAb, isolation of the troponin complex by immunoaffinity chromatography from muscle homogenate and
58 hain, cross-linked peptides were isolated by immunoaffinity chromatography from proteolytic digests o
59 from rod outer segments of bovine retinae by immunoaffinity chromatography in octyl glucoside was rec
60                           Anion exchange and immunoaffinity chromatography indicated that the (1-->4)
61                                              Immunoaffinity chromatography is one of the most powerfu
62 s of the protein to facilitate separation by immunoaffinity chromatography of overproduced mutant enz
63 e (EEF) tripepetide to allow purification by immunoaffinity chromatography on an immobilized monoclon
64 d from the soluble fraction by a single-step immunoaffinity chromatography procedure.
65                          Finally, we discuss immunoaffinity chromatography results that suggest the e
66 uid chromatography approach with preliminary immunoaffinity chromatography sample preparation.
67 extracts by a combination of traditional and immunoaffinity chromatography steps and found that the p
68 from HeLa cell extracts using two successive immunoaffinity chromatography steps.
69 olution mass spectrometry (MS) combined with immunoaffinity chromatography to determine quantitativel
70 nt signaling, we used cell fractionation and immunoaffinity chromatography to examine the physical en
71                  In this study, we have used immunoaffinity chromatography to identify proteins that
72 o identify new vaccine targets, we have used immunoaffinity chromatography to isolate class I HLA-A*0
73  pump-generated flow to deliver reagents and immunoaffinity chromatography to isolate the antigen fro
74                                      We used immunoaffinity chromatography to isolate the naturally p
75 nds the powerful technique of gentle-release immunoaffinity chromatography to many expressed proteins
76                                      We used immunoaffinity chromatography to measure the apoA-I conc
77 control children (n = 54), we used recycling immunoaffinity chromatography to measure the neuropeptid
78 f conventional chromatography and anti-SRCAP immunoaffinity chromatography to purify a native human S
79  and HBeAg, we used these Fabs in microscale immunoaffinity chromatography to purify HBeAg from indiv
80 urified from transformed Escherichia coli by immunoaffinity chromatography using a monoclonal antibod
81  for the proteolytic activity in the medium, immunoaffinity chromatography was performed.
82                                              Immunoaffinity chromatography was used to isolate the an
83                                           By immunoaffinity chromatography we enriched LeX glycoprote
84      Using a combination of ion exchange and immunoaffinity chromatography we have purified the gener
85 lf thymus pol delta preparations isolated by immunoaffinity chromatography were investigated.
86 ern blot analyses, immunohistochemistry, and immunoaffinity chromatography were used to detect and pu
87 compartments were seen following pulldown by immunoaffinity chromatography with Rab-specific antibodi
88 roteases inhibited by these serpins, we used immunoaffinity chromatography with serpin antibodies to
89 ication procedure (size, heparin, anion, and immunoaffinity chromatography): two heat shock proteins
90       This was accomplished by using on-line immunoaffinity chromatography, a reverse-phase LC separa
91                 We used trypsin proteolysis, immunoaffinity chromatography, and tandem mass spectrome
92 e unlabeled apoB:1000 particles, isolated by immunoaffinity chromatography, contained 56 PL, 8 TAG, a
93 usly pure mSR-BI-t1, prepared by single-step immunoaffinity chromatography, mediated high affinity HD
94                                        After immunoaffinity chromatography, the ORs are ~95% pure, an
95      Using a combination of conventional and immunoaffinity chromatography, we have successfully isol
96 n of endogenous levels of (FLAG)betabeta' by immunoaffinity chromatography, which was found to have 0
97 lecules from human plasma by on-line coupled immunoaffinity chromatography-asymmetric flow field-flow
98 rated in ripe fruit by gel filtration and by immunoaffinity chromatography.
99 e that had been purified and concentrated by immunoaffinity chromatography.
100 copy after 2-dimensional electrophoresis and immunoaffinity chromatography.
101 tion and 2) size exclusion-coupled anti-SOD1 immunoaffinity chromatography.
102 ast Saccharomyces cerevisiae and purified by immunoaffinity chromatography.
103 This was demonstrated by its isolation using immunoaffinity chromatography.
104 as mAbs and used to purify antigens by using immunoaffinity chromatography.
105  biochemically purified by sedimentation and immunoaffinity chromatography.
106 38 was associated with pol delta isolated by immunoaffinity chromatography.
107 bination of C(18) solid-phase extraction and immunoaffinity chromatography.
108 homogeneity in two steps by ion-exchange and immunoaffinity chromatography.
109 ns by conventional liquid chromatography and immunoaffinity chromatography.
110  by both standard biochemical techniques and immunoaffinity chromatography.
111 rom a pronase digest of Fap1 and purified by immunoaffinity chromatography.
112 orm have been purified from brain tubulin by immunoaffinity chromatography.
113 to detergent extraction and were purified by immunoaffinity chromatography.
114 orylated IGFBP-1 from normal human plasma by immunoaffinity chromatography.
115 y traditional solvent extraction followed by immunoaffinity clean-up.
116                        The sensitivity using immunoaffinity cleanup was approximately 100-fold greate
117 treatment and centrifugation, followed by an immunoaffinity column (IAC) clean-up step before mass sp
118       Assay validation was performed against immunoaffinity column (IAC) tandem reversed-phase high p
119  liquid-liquid extraction, clean-up using an immunoaffinity column (IAC), and identification by rever
120 the types of antibodies that are used in the immunoaffinity column and by using an appropriate detect
121 n in bronchoalveolar lavage and an anti-SNIP immunoaffinity column binds a 70-kDa protein in U937 cel
122                                           By immunoaffinity column chromatography, we have purified t
123 trong cation-exchange chromatography and N60 immunoaffinity column chromatography.
124 fects of human Abs affinity-purified (AF) by immunoaffinity column chromotography on excitation-contr
125                                     Using an immunoaffinity column comprised of immobilized monoclona
126 munoadsorption (EIA) of anti-Gal Ab using an immunoaffinity column of a Gal type 6 oligosaccharide de
127 ter two-dimensional gel electrophoresis, and immunoaffinity column purification, N-terminal amino-aci
128 lso detected in the proteins eluted from the immunoaffinity column using serpin-6 antibody.
129              The nonretained peaks from this immunoaffinity column were passed through a series inter
130                After purification through an immunoaffinity column, AFM1 is determined by HPLC-FLD.
131                                The developed immunoaffinity column/capillary electrophoresis microdev
132 S method against sample preparation using an immunoaffinity column; the recovery and specificity were
133    Ochratoxin A analyses were performed with immunoaffinity columns and detection by high performance
134 gel filtration and associated with RNAPII on immunoaffinity columns prepared with anti-CTD antibodies
135 C instrumentation after pre-separation using immunoaffinity columns that work through a mechanism of
136 native cleanup procedures (MultiSep and IAC--immunoaffinity columns) was performed, being the advanta
137 lidated by direct comparison with commercial immunoaffinity columns.
138 using millisecond-scale extractions on small immunoaffinity columns.
139 re co-purified with GAD by specific anti-GAD immunoaffinity columns.
140 anol/water (80:20; v/v) and cleaned up using immunoaffinity columns.
141  observation, we have developed a CD45-based immunoaffinity depletion method for removing CD45-contai
142                                        After immunoaffinity depletion of the most abundant serum prot
143 y, efficiencies of protein purification with immunoaffinity depletion were determined.
144 ll reproducibility of the process, including immunoaffinity depletion, is high, with a process replic
145 ity was achieved by applying front-end IgY14 immunoaffinity depletion.
146 or optimal experimental conditions to ensure immunoaffinity-enabled cell capture.
147 me of sensitive and resistant cells using an immunoaffinity-enriched mass spectrometry method.
148 erived tryptic peptide via high-flow peptide immunoaffinity enrichment and nanoflow LC-MS/MS.
149 inase ubiquitination using ubiquitin remnant immunoaffinity enrichment and quantitative mass spectrom
150                                              Immunoaffinity enrichment coupled with quantitative mass
151              Mass spectrometry combined with immunoaffinity enrichment detects protein microheterogen
152                                              Immunoaffinity enrichment of peptides coupled with analy
153 e methods to characterize the performance of immunoaffinity enrichment of peptides up to multiplex le
154  tryptic digestion of PAPs in suspension, an immunoaffinity enrichment of peptides, and LC-MS/MS-base
155 DAMTS-13 substrate (vWFh) was performed with immunoaffinity enrichment of the reaction substrate and
156   The assay combines magnetic bead-based NGF immunoaffinity enrichment using a non-neutralizing polyc
157        MALDImmunoassays-methods that combine immunoaffinity enrichment with matrix-assisted laser des
158 gh-resolution mass spectrometry coupled with immunoaffinity enrichment, we identified 47 lysine-acety
159 alytes and solutions to carry out integrated immunoaffinity extraction and electrophoretic separation
160                       A new method, based on immunoaffinity extraction coupled with liquid chromatogr
161                                              Immunoaffinity extraction integrated with matrix-assiste
162 nd by performing computer simulations of the immunoaffinity extraction of these drugs.
163                                By optimizing immunoaffinity extraction using monoclonal antibodies co
164 whole spot was dissolved prior to cleanup by immunoaffinity extraction, tryptic digest, and preconcen
165 agments were isolated from plasma samples by immunoaffinity extraction.
166                            The use of a dual immunoaffinity fluorescent (IAF) tag permitted this proc
167 mated using the VICAM AflaTest and OchraTest immunoaffinity fluorometric method in a total of 50 meat
168                           Application of the immunoaffinity fluorometric method is an accurate, safe
169                  The novel BoNT demonstrated immunoaffinity for anti-A monoclonal antibodies but did
170 s strain behaved as a typical BoNT/B, having immunoaffinity for anti-B monoclonal antibodies and clea
171 rofiltration into a microfluidic device with immunoaffinity for enhanced capture efficiency of CTCs.
172 from the liver was measured with a sensitive immunoaffinity/gas chromatography/high-resolution mass s
173 is presented, which involves coextraction by immunoaffinity (IA) beads and codetermination by selecte
174 pectrometry (LC/MS/MS) typically utilizes an immunoaffinity (IA) enrichment step such as immunoprecip
175                                              Immunoaffinity (IA) LC-MS/MS pharmacokinetic (PK) assays
176  assay was developed utilizing two different immunoaffinity (IA) reagents.
177 or the CTC-based cancer prognosis, relies on immunoaffinity interactions between CTCs and antibodies
178 chromatography/mass spectrometry analysis of immunoaffinity isolates of hippocampal neurons, that RAR
179                  In the present study, GLT-1 immunoaffinity isolates were prepared from rat cortex us
180 lial cell line with C muridarum, followed by immunoaffinity isolation and sequencing of MHC class I-
181                                   Rab5-based immunoaffinity isolation of IL-1beta-stimulated early en
182 ion of a pronase digestion step prior to the immunoaffinity LC-MS/MS allowed for measuring not only f
183              A highly specific and sensitive immunoaffinity LC-MS/MS assay for quantification of huma
184                                           An immunoaffinity LC-MS/MS assay has been developed to quan
185           This work provides precedence that immunoaffinity LC-MS/MS can effectively be used to measu
186 tadiene for 90 days, using a newly developed immunoaffinity liquid chromatography tandem mass spectro
187                                        Using immunoaffinity liquid chromatography-mass spectrometry,
188                                           An immunoaffinity liquid chromatography-tandem mass spectro
189                    This article describes an immunoaffinity liquid chromatography-tandem mass spectro
190                                           An immunoaffinity liquid chromatography-tandem mass spectro
191               We describe a novel, sensitive immunoaffinity liquid chromatography-tandem mass spectro
192                                     Using an immunoaffinity mass spectrometry approach, a whole famil
193                  Sera were adsorbed on a Gal immunoaffinity matrix, and tested for SLA haplotype spec
194                                     Using an immunoaffinity method, we purified an MDM2-associated pr
195 intestinal lipoproteins were separated by an immunoaffinity method.
196 of 180 ms between the sample and an anti-BSA immunoaffinity microcolumn and provided a signal within
197                                              Immunoaffinity monolith pretreatment columns have been c
198                                 Here, we use immunoaffinity phosphopeptide isolation coupled with mas
199       Finally, we combine this approach with immunoaffinity phosphotyrosine enrichment, enabling the
200 we demonstrate using a combination of online immunoaffinity-postconcentration-mass spectrometry in co
201 ic target for HSV-1 infection, and a protein immunoaffinity procedure, we enriched fully glycosylated
202                          These two different immunoaffinity procedures yielded very similar sets of p
203 , we used a discovery platform consisting of immunoaffinity profiling coupled to mass spectrometry th
204 tive phosphorylation of STAT5 and applied an immunoaffinity profiling strategy to identify tyrosine-p
205 can be recognized by specific antibodies for immunoaffinity purification (IAP) and subsequent identif
206                                        Using immunoaffinity purification (IP)-mass spectrometry (MS),
207 elles containing TrkB isolated from brain by immunoaffinity purification also contain dynein with IC-
208 eract with Kir2 channels, as demonstrated by immunoaffinity purification and affinity chromatography
209     Specificity of antibody was confirmed by immunoaffinity purification and immunoabsorption.
210                                              Immunoaffinity purification and mass spectrometry reveal
211                                        Using immunoaffinity purification and mass spectrometry we sho
212                                        Using immunoaffinity purification and mass spectroscopy, we id
213                                Here, we used immunoaffinity purification and quantitative mass spectr
214 loyed proteomic screening by phosphotyrosine immunoaffinity purification and tandem mass spectrometry
215 the A17 membrane protein was demonstrated by immunoaffinity purification and Western blot analysis.
216        Herein, we have developed and used an immunoaffinity purification assay to isolate endogenous
217                                        Using immunoaffinity purification coupled with liquid chromato
218                                        Using immunoaffinity purification followed by mass spectrometr
219 um freudenreichii subsp. shermanii and after immunoaffinity purification in extracts of cereal matric
220 pecific recognition of PEGylated species, an immunoaffinity purification method (IAP) using anti-PEG
221         One of these antibodies was used for immunoaffinity purification of a protein that was identi
222                      Furthermore, the simple immunoaffinity purification of ABCB6 to near homogeneity
223                                              Immunoaffinity purification of AtMC1-containing complexe
224 d the exomic sequences of eight tumors after immunoaffinity purification of cancer cells.
225 rategy that incorporates rapid and efficient immunoaffinity purification of Complex I followed by dif
226 tity of proteins analyzed by LC-MS following immunoaffinity purification of IsoLG-modified proteins.
227 -denaturing conditions has made possible the immunoaffinity purification of labile, multisubunit enzy
228      The key steps in this approach involved immunoaffinity purification of Myl3 from serum followed
229                                              Immunoaffinity purification of polyribosomes (polysomes)
230 dividual serpin-1 isoforms in plasma we used immunoaffinity purification of serpin-1 isoforms from M.
231            Cell lysis, DNA fragmentation and immunoaffinity purification of the desired protein will
232  we established that tcTPC allowed stringent immunoaffinity purification of the gamma-secretase compl
233 ed from the infected cells were subjected to immunoaffinity purification of the tagged proteins by ad
234                                              Immunoaffinity purification of this protein and microseq
235 at represent 3 Bcr-Abl fusion types by using immunoaffinity purification of tyrosine phosphopeptides
236 d signaling intermediates were identified by immunoaffinity purification of tyrosine-phosphorylated p
237 undertaken by two independent approaches: 1) immunoaffinity purification on a mAb raised to condition
238  of 8-oxo-dGuo observed were confirmed by an immunoaffinity purification stable isotope dilution ([(1
239                   Our microdevices couple an immunoaffinity purification step with rapid microchip el
240 ibody-induced hearing loss, we used antibody immunoaffinity purification to isolate the IESCA, which
241                                        In an immunoaffinity purification using anti-HDAC3, transcript
242                                        Using immunoaffinity purification we show that hMUS81 or hMMS4
243 cted human embryonal kidney (HEK) 293 cells, immunoaffinity purification, and mass spectrometry combi
244 d characterized by rate-zonal sedimentation, immunoaffinity purification, electron microscopy, and th
245                     Through a combination of immunoaffinity purification, immobilized metal affinity
246 n tested for immunofluorescence staining and immunoaffinity purification, leading to putative identif
247 means of a bottom-up analytical approach via immunoaffinity purification, tryptic digestion, and subs
248                                        Using immunoaffinity purification, we isolated ribosomal prote
249 RF-NH(2)) by mass spectrometry combined with immunoaffinity purification.
250 in to the DRM-H fragments is confirmed by co-immunoaffinity purification.
251                                  Analysis of immunoaffinity purified (ALA)284(GLU) and (SER)289(LEU)
252      To investigate its function further, we immunoaffinity purified a bestrophin complex from RPE ly
253 LA-A*11:01 harvested from infected cells was immunoaffinity purified and acid boiled to release heavy
254                                      PSA was immunoaffinity purified from 100 to 200 ml of serum from
255 ble complex containing MLL1 and MOF has been immunoaffinity purified from a human cell line that stab
256                           Proteins were also immunoaffinity purified from brain extracts using autoan
257    UDP-N-acetylglucosamine pyrophosphorylase immunoaffinity purified from encysting and non-encysting
258 tion and by PCR analyses of epithelial cells immunoaffinity purified from primary tumors.
259                  To test this hypothesis, we immunoaffinity purified PI4KIIalpha from isotope-labeled
260 d from six independent Mediator preparations immunoaffinity purified through their Nut2 (MED10), Med2
261            Slowly sedimenting nucleoids were immunoaffinity purified using antibodies to either of tw
262 eplication, was readily recovered along with immunoaffinity-purified 3A-FLAG.
263                             The receptor was immunoaffinity-purified and formed functional InsP3- and
264                                 Furthermore, immunoaffinity-purified anti-cardiolipin antibodies from
265 cDNA corresponding to the core protein of an immunoaffinity-purified arabinogalactan protein (AGP) se
266 rone assay after immunoprecipitation or with immunoaffinity-purified argpyrimidine-alpha-crystallin i
267 ugh acantholytic activities of each of these immunoaffinity-purified AuAbs could not induce a PV-like
268                       The target antigen was immunoaffinity-purified from skeletal muscle extracts an
269 referentially over preexisting GABA by using immunoaffinity-purified GABAergic SVs.
270 was used to analyze proteins associated with immunoaffinity-purified HDL from plasma obtained from 2
271                                              Immunoaffinity-purified hsBG from transfected COS-1 cell
272 es were exposed to various concentrations of immunoaffinity-purified leukotoxin and the cytotoxicity
273                           Electroelution- or immunoaffinity-purified MTB 19-kDa lipoprotein inhibited
274                            We show here that immunoaffinity-purified native PmpD exists as an oligome
275 dicate that OCP sera, OCP IgG fractions, and immunoaffinity-purified OCP autoantibodies react with th
276 m a keratinocyte expression library by using immunoaffinity-purified OCP autoantibody, encoded the cy
277                      The OP patient sera and immunoaffinity-purified OP sera, rabbit antisera against
278                                              Immunoaffinity-purified PS contained 1.4 +/- 0.6 Zn(2+)/
279                                    Employing immunoaffinity-purified Rho from affected RHO(T4R/T4R) d
280 from the brain and lung extracts, and in the immunoaffinity-purified sample, but not in the negative
281 rylated intermediate chains were enriched on immunoaffinity-purified Trk-containing organelles.
282        This method distinguishes itself from immunoaffinity resin-based approaches since it can be sc
283 ion, giving rise to materials referred to as immunoaffinity restricted access media (IA-RAM).
284 established, but they often depend on costly immunoaffinity sample clean-up.
285 cells were purified from spleens by negative immunoaffinity selection followed by flow sorting.
286                This method demonstrates true immunoaffinity separation of structurally related compou
287    The method involved analyte enrichment by immunoaffinity separation using anti-rhEPO antibody link
288 mprised analyte extraction and enrichment by immunoaffinity separation with anti-rhEPO antibodies, du
289      Liquid-solid extraction, clean-up using immunoaffinity solid phase extraction chromatography, an
290 roduced in culture by first incorporating an immunoaffinity step using monoclonal antibodies to purif
291                    Western blot analyses and immunoaffinity studies confirmed that this protein was b
292 time considerably exceeded that of classical immunoaffinity systems.
293 taking advantage of the rhodopsin C-terminal immunoaffinity tag common to all GPCR constructs.
294 enaturing detergent digitonin and a one-step immunoaffinity technique.
295  purified the putative ATPDase from liver by immunoaffinity techniques and obtained a heavily glycosy
296  by density gradient ultracentrifugation and immunoaffinity techniques specific to apolipoprotein B-1
297 boratory to use LC/MS/MS in conjunction with immunoaffinity techniques to evaluate candidate biomarke
298 has been approached by mass spectrometry and immunoaffinity techniques.
299 ted that the prepared insulin still kept its immunoaffinity to its antibody.
300 loped a novel workflow integrating DNA-based immunoaffinity with mass spectrometry to analytically va

 
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