ライフサイエンスコーパス: streptavidin

1 des that mimic key interactions of biotin to streptavidin.

2 rmation, and panned against the model target streptavidin.

3 form a complex that is held onto immobilized streptavidin.

4 nding to cis-divalent but not trans-divalent streptavidin.

5 n was immobilized for binding of Cy5-labeled streptavidin.

6 tinylated rhodium piano stool complex within streptavidin.

7 using gold nanoparticles (AuNPs), biotin and streptavidin.

8 rties, and strong interaction of biotin with streptavidin.

9 s M13 bacteriophage high selectivity for the streptavidin.

10 h low and high dissociation constant: biotin/streptavidin (10 fM) and HER2/HER2 antibody (0.44 +/- 0.

11 method to stepwise evolve peptide binders to streptavidin, a protein studied for over two decades and

12 incubated with increasing concentrations of streptavidin, achieving a limit of detection (LOD) of 5n

13 A standard biotin-streptavidin affinity model was tested using the MGNT ar

14 scribe a hybridization assay based on biotin-streptavidin affinity using lanthanide-labeled reporter

15 of the labeled extracts, trypsin digestion, streptavidin-affinity purification of peptides containin

16 specific binding affinity of the NCs toward streptavidin after incorporation.

17 Streptavidin-alkaline phosphatase was then conjugated to

18 These forms of streptavidin allow this key hub to be used with a new le

19 Results show that filling the MGNT with streptavidin altered the effective refractive index of t

20 oxyphenyl-functionalized SPCEs modified with streptavidin and a sandwich type immunoassay was impleme

21 es to pretargeting, strategies predicated on streptavidin and biotin, bispecific antibodies, compleme

22 a 2 x 2 junction array, functionalized with streptavidin and biotinylated antibodies specific for Es

23 onto a gold surface, covalent attachment of streptavidin and further immobilization of the biotinyla

24 Specifically, the competitive binding of streptavidin and goat anti-biotin for biotin-conjugated

25 ding silica nanoparticles (SNPs) coated with streptavidin and gold nanoparticles (AuNPs).

26 The bioassay sensor was then built up with streptavidin and subsequent biotinylated antibody.

27 wo different ligand-receptor systems (biotin/streptavidin and TNF-alpha) over a wide range of concent

28 age libraries to the N- or C-termini of core streptavidin and used them to setup phage-free noncompet

29 DNA anchors we attached a spherical protein (streptavidin) and a rod-shaped DNA (47bp) to a quartz cr

30 ntional fluorescently labeled antibodies and streptavidin, and fluorescent proteins.

31 ed by the covalent attachment of antibodies, streptavidin, and oligonucleotides and the binding and b

32 quantified using phycoerythrin (PE)-labeled streptavidin, and the fluorescence was analyzed in a Lum

33 followed by the layer-by-layer deposition of streptavidin, and then biotynilated capture probes.

34 of labeled biomolecules such as antibodies, streptavidin, and tubulin proteins and showed that stabl

35 tionalized by coating with polyethyleneimine-streptavidin-anti-Escherichia coli antibodies to improve

36 roscopy (MA/SERS), which utilizes a Fe3O4@Ag@streptavidin@anti-IgG nanocomposite with strong magnetic

37 enter of microcoils with functionalized anti-streptavidin antibody.

38 HA) amplification coupling with programmable streptavidin aptamer (SA-aptamer).

39 e oxidase, DNA/hydrogen peroxide, and biotin/streptavidin, are measured by the paper-based micro-calo

40 and analogues, with their strong binding to streptavidin, are used in many clinical laboratory tests

41 for doing this involved using membrane-bound streptavidin as a biomarker for the charge on the membra

42 a new desthiobiotin surface, using wild-type streptavidin as a robust bridge between the chip and the

43 nstrated by paper-printed tests and a biotin-streptavidin assay on a plastic substrate.

44 A towards a small peptide substrate carrying streptavidin at its distal end was also investigated to

45 We also show accumulation of model analyte (streptavidin at nanomolar concentration in nanoliter eff

46 The limiting step at present is binding of streptavidin at the end of DNA to biotin on capture bead

47 res of native-like cations of serum albumin, streptavidin, avidin, and alcohol dehydrogenase were pro

48 in-protein systems: biotin-avidin and biotin-streptavidin, barstar-dibarnase and Z domain-immunoglobu

49 f biotinylation sites identified compared to streptavidin-based enrichment of proteins.

50 re optionally sheared, affinity-purified via streptavidin bead immobilization, and subjected to tradi

51 and biotinylated proteins are enriched with streptavidin beads and identified by mass spectrometry.

52 and tagged RNA is biotinylated, captured on streptavidin beads and sequenced.

53 magnitude higher than previous results using streptavidin beads and the limit of detection (LOD) impr

54 2-aminoethyl methanethiosulfonate-biotin and streptavidin beads to determine their aqueous-accessibil

55 NA cross-linked to proteins were captured on streptavidin beads.

56 A complexes are then labeled with an enzyme (streptavidin-beta-galactosidase), and single enzymes ass

57 croring sensor was investigated using biotin-streptavidin binding as a model system.

58 labeled streptavidin is used to quantify the streptavidin binding capacity of each mesh type through

59 lent streptavidins enabled us to uncover how streptavidin binding depends on the nature of the biotin

60 ptide Strep-tag II in a manner comparable to streptavidin binding to biotin.

61 body-epithelial cell surface-binding, biotin-streptavidin binding, and the topologically enhanced cel

62 plemental biotin ingestion may affect biotin-streptavidin binding, leading to potential clinical misi

63 within or immediately after a 38-amino acid streptavidin-binding peptide (SBP) that is appended to t

64 ld-type AR tagged at its N terminus with the streptavidin-binding peptide epitope (streptavidin-bindi

65 says using truncated kinesin-1 motors with a streptavidin-binding peptide tag that can attach to stre

66 th the streptavidin-binding peptide epitope (streptavidin-binding peptide-tagged wild-type androgen r

67 ted to the highly specific bacterial protein streptavidin binds to biotinylated macromolecules like p

68 Strep-Tactin, an engineered form of streptavidin, binds avidly to the genetically encoded pe

69 material arrays to biosensing using standard streptavidin-biotin affinity model.

70 conjugated via biotinylated glycan (through streptavidin-biotin affinity) followed by linkage of hem

71 Both streptavidin-biotin and SATA/SMCC conjugation chemistrie

72 Although streptavidin-biotin binding affinity is described as the

73 Using a streptavidin-biotin binding system, we show that the det

74 to colloidal particles of different sizes by streptavidin-biotin bonds.

75 ike receptor-9 ligand-loaded particles using streptavidin-biotin cross-linking.

76 e complex immunoassays, including the use of streptavidin-biotin detection strategies.

77 bioreceptor layer was formed using a common streptavidin-biotin immobilization strategy and employed

78 and QD, and the high binding affinity of the streptavidin-biotin interaction, we achieved multiplexed

79 ce of MT minus ends labeled with dsDNA via a streptavidin-biotin interaction.

80 ntibody, or streptavidin: the high-stability streptavidin-biotin linkage improved sensitivity by an o

81 oated substrates and a strong but reversible streptavidin-biotin linkage to PEG-coated AFM tips enhan

82 ide probes were conjugated onto the UCPs via streptavidin-biotin linkage.

83 lymer that was attached to a surface through streptavidin-biotin linkage.

84 nal RIT (directly radiolabeled antibody) and streptavidin-biotin pretargeted RIT (PRIT) directed agai

85 in the limit-of-detection, the inclusion of streptavidin-biotin simplifies the development of simila

86 43, 75, and 292 for the IgG-antibody assay, streptavidin-biotin system, and covalently attached BSA,

87 rter to its target organelle, relying on the streptavidin-biotin system.

88 we found that integrin receptors dissociate streptavidin-biotin tethered ligands in focal adhesions

89 Based on the observation of streptavidin-biotin unbinding, we also conclude that the

90 ncentrations using a standard affinity model streptavidin-biotin.

91 advantages over traditional systems such as streptavidin-biotin.

92 The association constant (KA) for streptavidin/biotin and STV-NPs/biotin interactions obse

93 promising advance toward synthetic mimics of streptavidin/biotin.

94 representative protein-ligand binding pairs (streptavidin/biotin; IgG/anti-IgG) were quantified.

95 ayer surface (SAMs) was used for immobilized streptavidin-biotinylated probes on the sensor surface f

96 also solved the structure of trans-divalent streptavidin bound to biotin-4-fluorescein, showing how

97 The model protein streptavidin bound to horseradish peroxidase (HRP) was s

98 mate focusing position and separation of the streptavidin-bound biotin, anti-biotin-bound biotin, and

99 of biotinylated capture antibodies through a streptavidin bridge.

100 MNPs coated with streptavidin can combine with biotin labeled thrombin ap

101 This biotin-streptavidin capture strategy allows hydrogen/deuterium

102 Finally, lateral flow strips with a streptavidin capture test line and an anti-antibody cont

103 ) the classical assay that works with biotin-streptavidin chemistry, (II) the rapid assay that is per

104 s were immobilized on the surface via biotin/streptavidin chemistry.

105 first demonstration that recombinant peptide-streptavidin chimeras can be used for sensitive immunode

106 A bioanalytical workflow involving streptavidin chromatography and label-free quantitative

107 ctionalized (4FB) magnetic beads rather than streptavidin coated beads with a high density of capture

108 ement of optical read-out was obtained using streptavidin coated gold-nanoparticles interacting with

109 ary anti-S.aureus aptamer was immobilized on streptavidin coated magnetic beads (MB), which serves as

110 rotocol based on biotinylated DNA probes and streptavidin coated magnetic beads we were able to selec

111 nt of a 384-well immuno-PCR method that uses streptavidin coated on a PCR plate to capture complexes

112 ich assay, which employed nanoEnhancers (NIR-streptavidin coated quantum dots) for ultrasensitive det

113 rum with a fully automated platform based on streptavidin coated tips and a biotinylated mouse anti-h

114 duct can be trapped and purified directly in streptavidin coated wells.

115 n the ECM through bioconjugation between the streptavidin-coated beads and the collagen fibers and th

116 in-3 nanomolar binding partner, was bound to streptavidin-coated donor beads.

117 usly captured bacteria, and (III) binding of streptavidin-coated gold nanoparticles to the biotinylat

118 lated anti-human EGFR Apt was immobilized on streptavidin-coated magnetic beads (MB) and served as a

119 apture of biotinylated ligation junctions on streptavidin-coated magnetic beads and PCR amplification

120 lution and thus were further integrated into streptavidin-coated magnetic beads for purification of V

121 drug and catabolites were released from the streptavidin-coated magnetic beads, separated by monolit

122 the warhead, 8-base PNA strands, biotin, and streptavidin-coated magnetic beads, we demonstrate retri

123 oximity probes was directly immobilised onto streptavidin-coated magnetic beads.

124 nd the two antibodies is then captured using streptavidin-coated magnetic microparticles and directly

125 with a biotinylated secondary antibodies and streptavidin-coated MB resulted in a limits of detection

126 rase reaction products, which immobilized on streptavidin-coated microplate, hybridized with biotinyl

127 rinted in an array format onto the bottom of streptavidin-coated microtiter wells.

128 the basic sandwich type assay, performed in streptavidin-coated microtitration wells, the limit of d

129 on binding, the complex was harvested on the streptavidin-coated microwell, and subsequently the form

130 Stx binding to Pk analogues immobilized on streptavidin-coated plates was assessed by enzyme-linked

131 ling nanofiber meshes outperform traditional streptavidin-coated polystyrene plates under flow, valid

132 rategy that is enabled by the combination of streptavidin-coated quantum dot (QD) acceptors and bioti

133 the oriented immobilization of antibodies to streptavidin-coated surfaces, such that the antigen bind

134 d with the human adenosine deaminase (hADA1)-streptavidin complex and adenosine as a detection system

135 does not require dissociation of the biotin-streptavidin complex for protein retrieval.

136 Experiments with the biotin-streptavidin complex show that the predicted three-dimen

137 pported lipid bilayer via biotinylated lipid streptavidin complexes (pinning sites).

138 uding 23 assays that incorporated biotin and streptavidin components and 14 assays that did not inclu

139 nd 14 assays that did not include biotin and streptavidin components and served as negative controls.

140 against matched targets (carbonic anhydrase, streptavidin, concanavalin A) to identify desired ligand

141 beta-lactoglobulin and enolase), tetrameric (streptavidin, concanavalin A, and pyruvate kinase), and

142 tection from 10 nmol L(-1) to 320 pmol L(-1) streptavidin concentration with a much higher sensitivit

143 -ZnS core-shell nanocrystal quantum dot (QD) streptavidin conjugate donor and a Cy5 acceptor.

144 otinylated detection antibodies, fluorescent streptavidin conjugate, and wash buffer for a total volu

145 Furthermore, optical signal enhancement with streptavidin conjugated quantum dots was shown to yield

146 using secondary biotinylated antibodies and streptavidin-conjugated Au nanoparticles.

147 ction, which allows further elaboration with streptavidin-conjugated dyes or other molecules.

148 arbon electrode while is further linked to a streptavidin-conjugated HRP reporter.

149 s using biotinylated antibodies labeled with streptavidin-conjugated Pb- and Cd-based quantum dots (Q

150 et oligonucleotide followed by reaction with streptavidin-conjugated PbS QDs.

151 tramer technology and commercially available streptavidin conjugates.

152 It was found that streptavidin could inhibit the binding of goat anti-biot

153 geometry of the lipid layers, nucleation of streptavidin crystals occurred specifically on the DPN-p

154 By labelling a DNA replication fork with streptavidin (dsDNA end) and Fab (5' ssDNA) we located t

155 The model was tested with a streptavidin-dsDNA complex linked through biotin (small

156 ate the focusing behavior of Dylight labeled streptavidin (Dyl-Strep) proteins in the channel, using

157 R-Phycoerythrin (RPE) and Dylight labeled streptavidin (Dyl-Strep) were focused within a nanochann

158 mplexed with a biotinylated aptamer bound to streptavidin efficiently increased the SPR signal by com

159 These defined divalent streptavidins enabled us to uncover how streptavidin bin

160 ion that capitalizes on the high affinity of streptavidin for biotin but does not require dissociatio

161 ts, the biotinylated protein and HRP-labeled streptavidin for its detection.

162 ed a more powerful way to isolate monovalent streptavidin, for ultra-stable labeling without undesire

163 mine rates of DNA unwinding, displacement of streptavidin from biotinylated DNA, translocation on sin

164 h biotin to form a noncovalent link with the streptavidin functionalized AFM tip during the approach

165 linkers (BLs) to mediate the aggregation of streptavidin-functionalized gold nanoparticles (st-AuNPs

166 ffinity and the chemical characterization of streptavidin-functionalized gold nanoparticles (STV-NPs)

167 ed oligonucleotides) and (ii) the capture of streptavidin-functionalized gold nanoparticles to the af

168 Using a Chd1-streptavidin fusion remodeler, we found that targeting v

169 d lateral flow assay was based on the use of streptavidin gold nanoparticles for the labelling of the

170 Streptavidin has the advantage of rapid ultra-stable bin

171 ) the biotinylated detection antibody, (iii) streptavidin horseradish peroxidase, (iv) a wash buffer,

172 was then revealed by the introduction of the streptavidin-horseradish peroxidase conjugate that catal

173 SAH-CC with biotin used in conjunction with streptavidin-horseradish peroxidase.

174 er labeling the hybridized biotin-miRNA with streptavidin-HRP conjugates, amperometric detection at -

175 red biotinylated Nb or antigen was made with streptavidin-HRP.

176 n-labeled terminal of the probe bound to the streptavidin immobilized on the lateral flow test strip,

177 ect the presence of less than a femtomole of streptavidin in 10 muL of sample using fluorescence imag

178 The focusing position of streptavidin in electrophoretic-electroosmotic focusing

179 e-labeled amplicons, and fluorophore-labeled streptavidin in order to study the functionality and dis

180 ly be used to determine the concentration of streptavidin in solution at pM concentrations.

181 odel multivalent molecule, biotinylated anti-streptavidin, in PBS.

182 ersible decoration of DNA origami tiles with streptavidin, including revealing an encrypted Morse cod

183 ti-IL-17A catch antibodies, which via biotin-streptavidin interaction are bound to the biotinylated s

184 t a method based on the high affinity biotin-streptavidin interaction that allows selective capture o

185 argeting of tumors through the strong biotin-streptavidin interaction.

186 conjugated to the MMC surface through biotin-streptavidin interactions.

187 and conjugated to magnetic beads via biotin-streptavidin interactions.

188 nylated lectins were linked together through streptavidin interactions.

189 limit of detection for anti-DNP antibody and streptavidin is 1.2x10(-10) g/ml (0.55 pM) and 2.3x10(-1

190 The capture of biotin by streptavidin is an inspiration for supramolecular chemis

191 Streptavidin is one of the most important hubs for molec

192 Fluorescently labeled streptavidin is used to quantify the streptavidin bindin

193 t of the biotin-tagged tryptic peptides with streptavidin; (iv) liquid chromatography-tandem MS (LC-M

194 We have engineered streptavidin labelled Europium doped fluorescent silica

195 immobilized on polypyrrole matrix via biotin/streptavidin layer.

196 roach stage before the rupture of the biotin-streptavidin link.

197 vidin-binding peptide tag that can attach to streptavidin-loaded, supported lipid bilayers.

198 products by lambda-exonuclease digestion and streptavidin magnetic bead isolation.

199 ed and detected by the GMR sensor by linking streptavidin magnetic nanoparticles (MNPs) to the sensor

200 nvolving a sandwich hybridization assay onto streptavidin-magnetic beads (Strep-MBs), hybridization c

201 First, the streptavidin-magnetic nanobeads (MBs) were functionalize

202 Streptavidin-magnetic nanoparticles (streptavidin-MNPs)

203 ated cells, DNA end-labeling with biotin and streptavidin-mediated chemiluminescent detection of the

204 wide variety of molecules including dextran, streptavidin, microspheres, and lentivirus particles.

205 Streptavidin-magnetic nanoparticles (streptavidin-MNPs) are premixed with LAMP reagents inclu

206 Moreover, streptavidin mobility could be modulated.

207 d on the glassy carbon electrode (GCE) using streptavidin modified-gold nanoparticles/thiolated graph

208 enhanced Raman spectroscopy (MA-SERS) using streptavidin-modified magnetic nanoparticles (MNP@Strep)

209 As a platform for isolation process, streptavidin-modified MPs, which were conjugated via bio

210 , and finally allows the immobilization of a streptavidin-modified ruthenium-based ECL label via reac

211 the display of two to four Pk analogues per streptavidin molecule.

212 oups, enabling the molecule to be labeled by streptavidin molecules at these sites.

213 th a central scaffold protein linked to four streptavidin molecules, each having three pMHC ligands o

214 The IL-biotin-SAM efficiently formed a full streptavidin monolayer.

215 zol-4-yl)(biotin-cap-NBD-PE) lipids and that streptavidin more effectively outcompeted the anti-bioti

216 relying on fluorophore-conjugated monomeric streptavidin (mSA) to label membrane proteins carrying a

217 how that cross-linking of biotinylated HA in streptavidin multimers or supramolecular complexes with

218 biosensing of thrombin with the use of gold-streptavidin nanoparticles (strep-AuNPs) and silver redu

219 held even when the DNA duplex is tethered to streptavidin or the mobility of the nitroxides is altere

220 e demonstrated the quantitative detection of streptavidin over a broad range of concentrations down t

221 his work, using the well-acknowledged biotin-streptavidin pair as a benchmark, we go forward in the d

222 oteins cholera toxin B subunit-Alexa 647 and streptavidin-PE/Cy5, to membranes containing different a

223 Upon hybridization, a streptavidin-peroxidase (Strep-HRP) conjugate was employ

224 e reaction with the electrochemical reporter streptavidin-peroxidase conjugate.

225 When desired, however, streptavidin plus the biotinylated bait can be completel

226 -TGF and conjugation with peroxidase-labeled streptavidin (poly-HRP-Strept) polymer.

227 alized plasmonic AuNSs substrate but against streptavidin previously conjugated to gold nanorods, the

228 detect 526 ymol of the alkaline phosphatase streptavidin probe and accurately quantify zeptomole amo

229 strains engineered for enhanced tyrosine or streptavidin production.

230 (SAM) were designed and applied for binding streptavidin, promoting affinity biosensing and enzyme a

231 ct Transistor (FBI-OFET) sensor, embedding a streptavidin protein capturing layer, capable of perform

232 ollowing PVP removal, biotinylated thiol and streptavidin protein were added to the nanostars, which

233 A biotin-streptavidin pull-down assay showed that 4,11-bis(2-amin

234 by confocal microcopy after incubation with streptavidin quantum dots.

235 y remain nearly constant upon varying the Ir/streptavidin ratio [up to 78% ee (S)-salsolidine, kcat 2

236 on of S112 reveals a marked effect of the Ir/streptavidin ratio on both the saturation kinetics as we

237 mg/mL and temperature changes in biotin and streptavidin reaction are presented to demonstrate the f

238 e (LSPR) shift-based biosensors using biotin-streptavidin recognition interaction as a proof-of-conce

239 cis- and trans-divalent streptavidins retained tetravalent streptavidin's high t

240 DeNAno were selected against streptavidin-, rituximab- and bevacizumab-coated beads.

241 -divalent streptavidins retained tetravalent streptavidin's high thermostability and low off-rate.

242 The strong interaction between streptavidin (SA) and biotin is widely utilized in biote

243 advance is made possible by incorporating a streptavidin (SA) hydrogel capture/purification element

244 RP) for catalytic colorimetric assay and for streptavidin (SA)-biotin immunoassays.

245 Streptavidin (SA)-biotin pretargeted radioimmunotherapy

246 CD38 bispecific proved equal or superior to streptavidin (SA)-biotin-based CD38-SA PRIT.

247 amples of blank ImmunoCAPs coupled to either streptavidin (SA-CAP-1 or 2) or nonallergenic maltose-bi

248 oiety (Cp* = C5Me5(-)) within homotetrameric streptavidin (Sav) (referred to as Cp*Ir(Biot-p-L)Cl] su

249 To address these questions, we study streptavidin (SAv) binding to commonly used biotinylated

250 strate that a cysteine-containing variant of streptavidin (Sav) can serve as a protein host to model

251 otinylated iridium pianostool complex within streptavidin (Sav) isoforms was selected as a model reac

252 by developing a sequence-independent biotin-streptavidin (SAv) roadblocking strategy that simplifies

253 Using biotin-streptavidin (Sav) technology, artificial copper protein

254 ntigens pretreated with different bispecific streptavidin-scFv fusion proteins.

255 Similarly, streptavidin sensing shows the lowest detection of 1ngml

256 which self-assembles on gold film, afforded streptavidin sensing with surface plasmon resonance (SPR

257 By adding streptavidin-Sepharose beads to GL-biot-treated DU145 ce

258 iotinylated liposomes to surface-immobilized streptavidin show that the refractive index of the encap

259 iotin via click reaction and detected by the streptavidin-specific reporting signals.

260 to vastly extend the lifetime of a standard streptavidin SPR chip.

261 owing binding of a biotinylated antibody and streptavidin (StA) to the target cells.

262 ecific cell captures using a micro-patterned streptavidin (STR)-functionalized silicon nanowire (SiNW

263 We developed a modular RNA aptamer-streptavidin strategy, termed S1mplex, to complex CRISPR

264 ium exchange quench conditions by the biotin-streptavidin strategy.

265 e we report the solution of a selenobiotinyl-streptavidin structure using phases obtained by the anom

266 amers for malachite green (MG), spinach, and streptavidin (STV).

267 successfully fused to the C-terminus of Dead streptavidin subunits.

268 with biotin, which was used as a ligand for streptavidin (SV) detection.

269 ilized on the copolypyrrole layer via biotin-streptavidin system.

270 eterologous cargos along DNA, for example, a streptavidin tetramer.

271 we present an efficient approach to isolate streptavidin tetramers with two biotin-binding sites in

272 ptors (EGFR) using biotinylated EGF bound to streptavidin that is covalently coupled in an ordered ar

273 beads with Protein L, secondary antibody, or streptavidin: the high-stability streptavidin-biotin lin

274 When bound to streptavidin, this compound cannot cross the plasma memb

275 olved the crystal structures of cis-divalent streptavidin to 1.4A resolution and trans-divalent strep

276 avidin to 1.4A resolution and trans-divalent streptavidin to 1.6A resolution, validating the isolatio

277 sive activated SA-aptamers could capture the streptavidin to achieve enhancement and output of the de

278 However, the ability of streptavidin to bind four biotinylated molecules in a he

279 biotinylated liposomes are attached through streptavidin to biotinylated capture probes.

280 This caused the focusing position of streptavidin to migrate toward the negatively charged el

281 The binding of coexpressed streptavidin to SBP causes signal masking, whereas addit

282 ation of three tetrameric protein complexes (streptavidin, transthyretin, and hemoglobin) in the gas

283 phycoerythrin-biotin (PhycoE-Biotin) and Cy5-streptavidin trapped in the two proteoliposome populatio

284 hesized and subsequently functionalized with streptavidin (UCP-strep).

285 Rupture forces comparable to biotin:streptavidin unbinding were observed.

286 Here we combined traptavidin (a streptavidin variant maximizing biotin binding strength)

287 tegy and explaining the behavior of the Dead streptavidin variant.

288 n detecting a high molecular weight analyte (streptavidin) versus in the flow-over PSi approach.

289 Streptavidin was chosen as an initial target to establis

290 on (LOD) of the MGNT arrays for detection of streptavidin was estimated as 25nM, with a detection tim

291 inylated reporter antibody and reaction with streptavidin was selected.

292 atch crystallization screening setups, where streptavidin was used as a model protein for crystalliza

293 Horseradish peroxidase-conjugated streptavidin was used to detect the biotinylated collage

294 ffinities of biotin and desthiobiotin toward streptavidin, we demonstrate selective and reversible de

295 As a result, the H1-H2 complexes and streptavidin were attached to the sensor surface, leadin

296 In our experiment, microbeads coated with streptavidin were driven to the sensors in the center of

297 rations (4.17pM to 41.7nM) of dye-conjugated streptavidin were simultaneously infused through the sec

298 tinylated substrate that, when captured with streptavidin, were resistant to challenge with competito

299 lymers with the ability to specifically bind streptavidin while minimizing the nonspecific binding of

300 y and 4,7-dihydroxy-1,10-phenanthroline into streptavidin yields an NAD(P)H-dependent artificial tran