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1 chia coli and then purified by metal chelate affinity chromatography.
2 erexpressed protein by immobilized metal ion affinity chromatography.
3 otein (CabP) in S. pneumoniae using c-di-AMP affinity chromatography.
4 was purified by nickel-nitrilotriacetic acid affinity chromatography.
5  cells and purified by immobilized metal ion affinity chromatography.
6     The enzyme was purified using cobalt ion affinity chromatography.
7 ed immunoprecipitation and immobilized metal affinity chromatography.
8 lated from crude cell membrane fractions via affinity chromatography.
9 he detergent Fos-choline-12, and purified by affinity chromatography.
10 teases can be exploited for highly selective affinity chromatography.
11 coli and purified to homogeneity by means of affinity chromatography.
12 per motif transcription factor, by G-box DNA affinity chromatography.
13 ied by nickel-nitrilotriacetic acid (Ni-NTA) affinity chromatography.
14 f immobilized metal affinity and metal oxide affinity chromatography.
15 m a variety of species and tissue sources by affinity chromatography.
16 binant His(6)-tagged TcNr was purified by Ni affinity chromatography.
17 and easily purified from Escherichia coli by affinity chromatography.
18 glycated species can be enriched by boronate affinity chromatography.
19  tag, and the protein was purified by nickel affinity chromatography.
20 in surface labeling followed by streptavidin-affinity chromatography.
21  antibodies were removed from immune sera by affinity chromatography.
22  and mTORC2 from HEK-293 cells using FLAG-M2 affinity chromatography.
23  Neurexin1 as a receptor for LRRTM2 based on affinity chromatography.
24 endothelial Ag, in this study purified by Ab-affinity chromatography.
25 nt PrtP copurifies with PrcB-6xHis in nickel affinity chromatography.
26  purified from a bacterial host using nickel affinity chromatography.
27  chromatography and immobilized bTf antibody affinity chromatography.
28 s purified from human placental membranes by affinity chromatography.
29 rs and CUG-BP1 to the exonic silencer by RNA affinity chromatography.
30 lene glycol precipitation followed by lectin affinity chromatography.
31 g to CCPs 7-8 and 19-20 bind well in heparin-affinity chromatography.
32 lot and ELISA, and OPN was purified using Ni affinity chromatography.
33 in E. coli, and purified with Ni-NTA agarose affinity chromatography.
34 teins to aid in their purification via metal affinity chromatography.
35 rotein could be purified in a single step by affinity chromatography.
36  (DE3) and purified the enzyme by cobalt ion affinity chromatography.
37 ich might have been co-purified during metal affinity chromatography.
38 sed recombinantly in E. coli and purified by affinity chromatography.
39 estimates of dissociation constants and FcRn affinity chromatography.
40 uent pulldown experiments with biotin-avidin affinity chromatography.
41 re exploited to purify the native protein by affinity chromatography.
42 red by surface plasmon resonance and heparin affinity chromatography.
43 and purified by nickel-nitrilotriacetic acid affinity chromatography.
44 nium sulfate precipitation, ion exchange and affinity chromatography.
45 e, A1AT (Zemaira) or M-type A1AT purified by affinity chromatography.
46 sed in a heterologous system and purified by affinity chromatography.
47 ividual conformers could be isolated by bNAb affinity chromatography.
48 xpressed in Escherichia coli and purified by affinity chromatography.
49 mplex purified under anaerobic conditions by affinity chromatography.
50 PSF) as an interacting protein with Fox-3 by affinity-chromatography.
51 que that couples isotachophoresis (ITP) with affinity chromatography (AC) to achieve rapid, selective
52 dy of coupling of isotachophoresis (ITP) and affinity chromatography (AC) to effect rapid, selective
53  extract or a plant total protein extract by affinity chromatography against smGN.
54              Using glutathione-S-transferase affinity chromatography, AgmU was found to interact eith
55 cific IgGs from four representative sera via affinity chromatography, allowing us to determine the co
56                                The 10.1.1 Ab-affinity chromatography also purified LFA-1, an integrin
57 ication as well as tandem size exclusion and affinity chromatography analyses provided the first bioc
58  specifically interacts with DnaA protein by affinity chromatography and a solid phase binding assay,
59 nrich the modified peptides by avidin-biotin affinity chromatography and analyze them by nanoRP-UPLC-
60 ng Fab/Rev complex was purified by metal ion affinity chromatography and characterized by analytical
61 rs, secreted into culture media, purified by affinity chromatography and characterized by biolayer in
62 n, as demonstrated by 1) binding assays (DNA affinity chromatography and ChIP) showing specific IGF-I
63                                          DNA affinity chromatography and chromatin immunoprecipitatio
64 associate with human DNA polymerase delta by affinity chromatography and coimmunoprecipitation assays
65 nteraction assays of recombinant kinases and affinity chromatography and competition affinity assays.
66                                              Affinity chromatography and cross-linking experiments sh
67   To study resin fouling in situ, we coupled affinity chromatography and Fourier transform infrared (
68 essed in E. coli, purified by Ni-NTA agarose affinity chromatography and functionally characterized i
69 y by anion exchange chromatography, His-Trap affinity chromatography and gel filtration.
70                              Moreover, using affinity chromatography and gel shift assays, we demonst
71                              Here, employing affinity chromatography and glycerol gradient centrifuga
72 e-catecholic adducts, that were separated by affinity chromatography and high performance liquid chro
73 he crosslinking activity was purified by RNA affinity chromatography and identified as nucleolin by m
74                      By using phosphoprotein affinity chromatography and immunoblot analyses, we show
75                                      Heparin affinity chromatography and intrinsic fluorescence kinet
76            To address this question, we used affinity chromatography and isoelectric focusing to frac
77 enient purification by immobilized metal-ion affinity chromatography and labeling with [(99m)Tc(CO)3]
78 hese common alleles, we used oligonucleotide affinity chromatography and liquid chromatography-mass s
79                                  Here, using affinity chromatography and mass spectrometry experiment
80                                          DNA affinity chromatography and mass spectrometry identified
81                                              Affinity chromatography and mass spectrometry identified
82                                      We used affinity chromatography and mass spectrometry to discove
83                                        Using affinity chromatography and mass spectrometry we identif
84                                        Using affinity chromatography and mass spectrometry we reveale
85                                    Using RNA-affinity chromatography and mass spectrometry, we furthe
86                           By combining siRNA affinity chromatography and mass spectrometry, we have i
87                                        Using affinity chromatography and mass spectrometry, we identi
88                                        Using affinity chromatography and mass spectrometry, we identi
89                                        Using affinity chromatography and mass spectrometry, we identi
90                              Here, employing affinity chromatography and mass spectrometry, we identi
91                                              Affinity chromatography and proteomics analysis using KS
92 Using a combination of immunohistochemistry, affinity chromatography and proteomics, we identified th
93  in human plasma were confirmed by employing affinity chromatography and proteomics.
94 c binding proteins were identified by Zn(2+)-affinity chromatography and proteomics.
95 ralogs, whose composition we corroborated by affinity chromatography and proximity labeling mass spec
96                                        Using affinity chromatography and split-Yellow Fluorescent Pro
97 -enriched fractions, using immobilized metal affinity chromatography and tandem mass spectrometry.
98                            Immobilized metal affinity chromatography and titanium dioxide chromatogra
99 Yersinia pseudotuberculosis were purified by affinity chromatography and used as immunogens to determ
100 3 proteins were not detected in the RNP, but affinity chromatography and yeast two-hybrid experiments
101 r derivatized to IMAC (immobilized metal ion affinity chromatography) and is investigated by loading
102 hia coli, purified in a one-step fashion via affinity chromatography, and activity as well as specifi
103 e enzyme-linked immunosorbent assay (ELISA), affinity chromatography, and bio-layer interferometry (B
104 expression, purified using immobilized metal affinity chromatography, and characterized for T cell bi
105 a pastoris, purified the proteins via tandem affinity chromatography, and determined MDR3-specific AT
106 ecipitation and nickel-nitrilotriacetic acid affinity chromatography, and further supported by co-loc
107 bsence of denaturation and fixation, heparin-affinity chromatography, and high-resolution LC-MS/MS, a
108 munoaffinity purification, immobilized metal affinity chromatography, and nanoflow liquid chromatogra
109 vels in Escherichia coli, purified by nickel affinity chromatography, and partially characterized.
110 tagenesis, coupled with splicing assays, RNA-affinity chromatography, and protein overexpression, and
111 erum IgGs were subjected to standard antigen-affinity chromatography, and resulting elution, wash, an
112 riched by detergent phase separation, lectin affinity chromatography, and SDS-PAGE.
113                          CPO was purified by affinity chromatography, and the purified enzyme was abl
114 purified from seeds, were separated by metal affinity chromatography, and their properties (GTPase ac
115 s like enzyme-linked immunosorbent assay and affinity chromatography are commercially available for t
116  native gel electrophoresis, traditional and affinity chromatography assays and surface plasmon reson
117     When AUG3 was enriched from seedlings by affinity chromatography, AUG1 was detected by immunoblot
118 ly(dimethylsiloxane) (PDMS), implements cell-affinity chromatography based on the selective cell-capt
119   Two fractions of transferrin, separated by affinity chromatography based on their binding or not to
120 arose bead-based microfluidic device for the affinity chromatography-based capture and detection of R
121     A simple, cheap, and highly reproducible affinity chromatography-based method has been developed
122                                  Here, using affinity chromatography, bioinformatics analyses, NAD sy
123                             In addition, MAb affinity chromatography can be expensive, the necessary
124 emonstrated for the first time how anti-IgG4 affinity chromatography can be used to prepare physiolog
125 easured using three primary assays (boronate-affinity chromatography, capillary isoelectric focusing
126 atographic phase to create cellular membrane affinity chromatography (CMAC) columns, CMAC(1321N1) and
127 ationary phase to form two cellular membrane affinity chromatography (CMAC) columns, CMAC(hOCT1(G465R
128 ey specifically interact, as demonstrated by affinity chromatography, co-immunoprecipitation, biosens
129                                        Using affinity chromatography, coimmunoprecipitation, retaggin
130 irst time, the implementation of a Protein-A affinity chromatography column as the first dimension ((
131 i-CD14, or anti-CD19 antibodies were used as affinity chromatography columns to separate target blood
132 gh reconditioning power of protein G'e-based affinity chromatography columns.
133 ins from human U2OS osteosarcoma cells using affinity chromatography coupled to mass spectrometry emp
134                                        Using affinity chromatography coupled to multidimensional prot
135 we describe the use of peptide aptamer-based affinity chromatography coupled with mass spectrometry t
136                                 Using ligand-affinity chromatography coupled with mass spectrometry,
137                    Toward this goal, we used affinity chromatography coupled with proteomics technolo
138 tor (NF) 90 and NF45, as demonstrated by DNA affinity chromatography coupled with tandem mass spectro
139           With the detergent assisted lectin affinity chromatography (DALAC), a total of 1491 protein
140 xample, to fluorescent tags or 'handles' for affinity chromatography--directly on complex molecular s
141 ifications of carbon; potential uses include affinity chromatography, DNA sequencing technologies, bi
142 ied a set of V-genes heavily enriched in the affinity chromatography elution, constituting the serum
143   Tryptic phosphopeptides (immobilized metal affinity chromatography-enriched) were identified and qu
144                                              Affinity chromatography experiments identified the prima
145                                      We used affinity chromatography experiments to uncover specific
146                                     Finally, affinity chromatography experiments using peptides corre
147                                              Affinity-chromatography experiments revealed that the ly
148 d by gel-shift assay and affinity by frontal affinity chromatography (FAC).
149 2D) analytical system consisting of boronate-affinity chromatography followed by CIEF.
150                                              Affinity chromatography followed by mass spectrometry an
151 ing partners for CaBP5 were identified using affinity chromatography followed by mass spectrometry an
152 d a comprehensive set of Drosophila Rabs for affinity chromatography followed by mass spectrometry to
153 ocedure that combines membrane flotation and affinity chromatography for the purification of autophag
154 igned a metal-directed immobilized metal ion affinity chromatography for the sequential enrichment of
155 '-UTR) binding proteins were purified by RNA affinity chromatography from cytosolic fractions of TNF-
156  The recombinant human Hsp72 was purified by affinity chromatography from insect cells, and purity wa
157 een isolated by origin sequence-specific DNA affinity chromatography from total chloroplast proteins.
158 (v)1.2 channels by CaBP5 were analyzed using affinity chromatography, gel overlay assays, and patch-c
159                                        Using affinity chromatography, HCR/F bound native synaptic ves
160  system, named High Performance Multi-Lectin Affinity Chromatography (HP-MLAC), is composed of a seri
161 e rates involves the use of high-performance affinity chromatography (HPAC) and estimates of band-bro
162 ons with these particles by high-performance affinity chromatography (HPAC).
163  cow's milk (n=25) by a previously validated affinity chromatography-HPLC method.
164                 FA was also quantified by an affinity chromatography-HPLC method.
165                                              Affinity chromatography identified 74 ZMP-binding protei
166  Ligands were purified by size exclusion and affinity chromatography, identified by proteomic mass sp
167 ichment by TiO2 and Ti(4+)-immobilized metal affinity chromatography (IMAC) by a single operator.
168 t as has been reported for immobilized metal affinity chromatography (IMAC) columns.
169 C) employing gallium-based immobilized metal affinity chromatography (IMAC) in conjunction with titan
170 etry-compatible, iron(III)-immobilized metal affinity chromatography (IMAC) methods that use either n
171 ng phosphopeptides include immobilized metal affinity chromatography (IMAC) or titanium dioxide (TiO2
172  through complexation with immobilized metal affinity chromatography (IMAC) resin.
173 e sequential Ga(3+)-Fe(3+)-immobilized metal affinity chromatography (IMAC) strategy displayed a 1.5-
174                    Second, immobilized metal affinity chromatography (IMAC) takes advantage of phosph
175                        Immobilized metal-ion affinity chromatography (IMAC) used to purify recombinan
176         On the other hand, immobilized metal affinity chromatography (IMAC) was used to quantify thes
177                        Immobilized metal ion affinity chromatography (IMAC) with nickel-NTA was used
178 hosphopeptides through immobilized metal ion affinity chromatography (IMAC), followed by enrichment o
179 ied in a single step using Immobilized Metal Affinity Chromatography (IMAC), in-solution trypsin dige
180 5-/- embryos, using an Immobilized Metal-Ion Affinity Chromatography (IMAC), which specifically binds
181  TRAIL was accomplished by immobilized metal affinity chromatography (IMAC), which was followed by tr
182 ptides were isolated using immobilized metal affinity chromatography (IMAC).
183 ed by protective antibodies, we selected, by affinity chromatography, immunoglobulins against immobil
184                                              Affinity chromatography, immunoprecipitation, enzyme-lin
185                           Analysis by lectin-affinity chromatography in conjunction with gas chromato
186                                        Using affinity chromatography in conjunction with tandem mass
187 +/- 0.4 muM) and close to that determined by affinity chromatography in the literature (6 +/- 3 muM).
188 n, we developed an approach that uses lectin affinity chromatography, ion-exchange chromatography, hy
189                            Cellular membrane affinity chromatography is a technique that is based on
190        Cell separation based on microfluidic affinity chromatography is a widely used methodology in
191                                       Lectin affinity chromatography (LAC) has evolved as a powerful
192                                           In affinity chromatography, lengsin also bound the equivale
193 ibody and protein A with in-line multilectin affinity chromatography (M-LAC) which consists of three
194 rboxyl terminus of AbgB and subsequent metal affinity chromatography (MAC).
195 ules, which can be further purified by metal affinity chromatography (MAC).
196               DNA binding assays, liquid and affinity chromatography, MALDI-MS analysis, and de novo
197 ure in each candidate small molecule enables affinity chromatography-mass spectrometry, which produce
198 protein conjugates formed were identified by affinity chromatography-mass spectrometry.
199 IBA) column as a viable small-molecule-based affinity chromatography method for antibody purification
200                     Here we describe a novel affinity chromatography method that utilizes the NBS as
201                                        A new affinity chromatography method was developed by modifyin
202 tion with titanium dioxide-based metal oxide affinity chromatography (MOAC).
203                                   Using FcRn affinity chromatography, molecular dynamics simulation,
204 , enzymatic assays, fluorescence microscopy, affinity chromatography, MS, and FRET analyses, we ident
205                                           Ni affinity chromatography of a mixture of E. coli (His)(6)
206 odextrin (beta-CD) is extremely effective in affinity chromatography of prenylated proteins.
207    All steps including immobilized metal ion affinity chromatography of protein on cobalt-loaded bead
208               Arginine-glycine-aspartic acid affinity chromatography of proteins from the ungerminate
209                                     By IL-34 affinity chromatography of solubilized mouse brain membr
210 ase-specific COMP fragments were isolated by affinity chromatography of synovial fluids from patients
211                                        Con A affinity chromatography of the Df extract revealed that
212                                 Here we used affinity chromatography of tumor cell extracts to identi
213 ctin was purified from the coelomic fluid by affinity chromatography on a GlcNAc-derivatized column a
214 ilized broad-spectrum kinase inhibitors, (3) affinity chromatography on immobilized (R)-roscovitine a
215    Using ammonium sulphate precipitation and affinity chromatography on pepstatin-A agarose bed the a
216        IgG was isolated from serum/plasma by affinity chromatography on Protein G.
217 ted proteins in the male genital tract using affinity chromatography on PSG2, an anti-sulfotyrosine m
218 lin from serum, involving PEG precipitation, affinity chromatography on Sepharose derivatized with ac
219         Purification of tumor homogenates by affinity chromatography on these peptides and subsequent
220 n this paper, an open-tubular capillary cell affinity chromatography (OT-CAC) method to enrich and se
221 tion system with open-tubular capillary cell affinity chromatography (OT-CAC), although any separatio
222            Compared to immobilized metal-ion affinity chromatography, PRISM provided approximately 10
223 ahistidines are very common tags used in the affinity chromatography purification of recombinant prot
224 ruct was further pursued for optimisation of affinity chromatography purification.
225 dem Mass Spectrometry (LC-MS/MS) analysis of affinity chromatography purified antigens resulted in id
226 f heterologously expressed and metal-chelate-affinity chromatography-purified ZmEXPB6 on growth-reduc
227 industrial scale, replacing fouled Protein A affinity chromatography resin accounts for a large propo
228 r device requires only microliter volumes of affinity chromatography resin-a condition that maximizes
229 B was coated onto an IMAC (immobilized metal affinity chromatography) resin and successfully bound Co
230 is by similarity search, protein arrays, and affinity chromatography revealed four native ligand-rece
231 itochondrial membrane of T. brucei by tandem affinity chromatography revealed that TbTim17 associates
232 dem affinity purification vector followed by affinity chromatography, SDS-PAGE, and identification of
233 can be improved by application of a combined affinity chromatography shotgun immunoproteomic approach
234                                          CaM-affinity chromatography showed that CaM binding to KCa3.
235                                              Affinity chromatography showed that the CendR peptides b
236                                              Affinity chromatography showed the binding of the TonB C
237 tial elution protocol from immobilized metal affinity chromatography (SIMAC) employing gallium-based
238   Overexpressed SHI was purified by a single affinity chromatography step using the Strep-tag II, and
239 eptide affinity just as antibodies, using an affinity chromatography strategy.
240  Optical methods include fluorescent frontal affinity chromatography, surface plasmon resonance metho
241 otein in mycobacterial species, and by using affinity chromatography techniques, we identify specific
242 urified from seabuckthorn seeds using chitin-affinity chromatography that showed antifreeze property
243                                        Using affinity chromatography, the authors identified Munc18-1
244 enrichment by Ub-affinity and nickel chelate-affinity chromatography, the ubiquitylated proteins were
245                                    Using RNA affinity chromatography, three members of the heterogene
246 an alpha(2)beta(2)gamma(2) hexamer by nickel affinity chromatography through a "His(6)" affinity tag
247  capillary isoelectric focusing and boronate affinity chromatography to assess the formation and diss
248 m BsAbs that were purified through protein A affinity chromatography to demonstrate industrial applic
249 phosphopeptide enrichment materials based on affinity chromatography to either immobilized metals (IM
250 etry-based workflow that incorporates lectin affinity chromatography to enrich for proteins that carr
251 on of titanium dioxide and immobilized metal affinity chromatography to enrich phosphopeptides, we ex
252 ded protein was then re-isolated by means of affinity chromatography to identify and quantify the cap
253                     We subsequently used RNA affinity chromatography to identify Mbnl1 as a splicing
254                   In this study, we used RNA affinity chromatography to identify trans factors that b
255                                 We have used affinity chromatography to isolate these antibodies and
256                       Here, we used gelsolin affinity chromatography to purify actin from fission yea
257 ecombinant hSMVT in Pichia pastoris and used affinity chromatography to purify the detergent-solubili
258 geneous RNCs are isolated by combining metal affinity chromatography (to isolate ribosome-bound speci
259        Moreover, the chip could function as "affinity chromatography" to identify bioactive phytochem
260 peptide, was purified to near homogeneity by affinity chromatography under native conditions.
261 in was purified from the bacterial lysate by affinity chromatography using a biotinylated promoter re
262 ly, the hydrazide product can be enriched by affinity chromatography using aldehyde resins, thus dras
263 ding to the SOSIP.664 design and purified by affinity chromatography using broadly neutralizing antib
264 b) was separated and quantitated by boronate affinity chromatography using optimized shielding reagen
265                                              Affinity chromatography using patient-derived mAbs ident
266 phosphoethanolamine and could be purified by affinity chromatography using phosphoethanolamine-conjug
267                                        Metal affinity chromatography using polyhistidine tags is a st
268                                      Through affinity chromatography using primary neutrophil lysate,
269 change chromatographies and then purified by affinity chromatography using Sepharose-immobilized kiwi
270    To identify binding factors, we conducted affinity chromatography using the A-box element and foun
271 targets in an unbiased fashion, we performed affinity chromatography, using tandem liquid chromatogra
272 ile Cic was not identified through our A-box affinity chromatography, utilization of the same site, t
273                                              Affinity chromatography utilizing histidine tagged sV23
274                                         Weak affinity chromatography (WAC) was recently introduced as
275                                    Here, RNA affinity chromatography was used to isolate cellular pro
276           Additionally, tandem nickel-cobalt affinity chromatography was used to prepare highly purif
277 tal proteomics approach involving dye-ligand affinity chromatography, we confirm NTP binding to 47 di
278             Using HeLa cell extracts and DNA affinity chromatography, we demonstrate that RPA is pref
279                                     By using affinity chromatography, we find that Arl8-GTP binds to
280                                        Using affinity chromatography, we identified alpha- and beta-n
281                                 Using T(1)AM-affinity chromatography, we isolated this protein, and s
282          Using surface plasmon resonance and affinity chromatography, we show here that the second lu
283            Here, using a live cell assay and affinity chromatography, we show that huntingtin has a k
284  expression in yeast and purification by CaM-affinity chromatography, we show that, unlike other ACAs
285           IPR proteins isolated by I-peptide affinity chromatography were identified by proteomics as
286 glycated materials, separated using boronate affinity chromatography, were fully characterized using
287 The columns were characterized using frontal affinity chromatography with [(3)H]-epibatidine as the m
288 step method to purify native-like trimers by affinity chromatography with a trimer-specific bNAb, PGT
289 xpressed in Escherichia coli and purified by affinity chromatography with a yield of 100 mg/liter.
290 either fluorescence spectrometry or boronate affinity chromatography with detection by specific fluor
291 c acid (NMDA), was established using frontal affinity chromatography with flunitrazepam and diazepam
292 tone biotinylation, and enrichment by avidin affinity chromatography with mass spectrometry.
293                                 Here we used affinity chromatography with non-catalytic Coa and vWbp
294 in more weakly than wild-type as observed by affinity chromatography with scaffolding protein-agarose
295                                    Using RNA affinity chromatography with the 3'-untranslated region
296 that interact with this domain, we performed affinity chromatography with the recombinant intracellul
297 l antibodies by combining the selectivity of affinity chromatography with the simplicity of salt-indu
298 n of partially assembled F(O)F1 complexes by affinity chromatography with the use of mutants synthesi
299 action of CaBP4 and Unc119 was studied using affinity chromatography, yeast two-hybrid system, coimmu
300  the precursor protein, followed by negative affinity chromatography, yielded a purified peptide.

 
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