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1 ich expressed one of the ATPases tagged with hexahistidine.
2 aining the photo-tag: 4-benzoylbenzyl-glycyl-hexahistidine.
3 uitin (Ub) monomers N-terminally tagged with hexahistidine.
4 toplasmic proteins expressing the ubiquitous hexahistidine affinity handle can be specifically attach
5                    Simultaneous display of a hexahistidine affinity tag, the MAL1 epitope and the gre
6 litated by the inclusion of a tag containing hexahistidine and a short biotinylation sequence.
7 m-affinity purification (TAP) approach using hexahistidine and BirA-specific biotinylation tags for i
8 ith a hexahistidine tag at the N terminus or hexahistidine and c-myc tags at the C terminus was able
9                         yk91g4 tagged with a hexahistidine and DLYDDDDK peptide epitope was expressed
10 using a strategy based on two affinity tags (hexahistidine and FLAG) engineered into the N terminus o
11 ing analysis was facilitated by insertion of hexahistidine and short biotinylation sequences on the d
12 eceptors extended on the amino terminus with hexahistidine and the FLAG epitope, DYKDDDDK (H/F-A(2B))
13 te that was chemoselectively modified with a hexahistidine-appended peptide.
14                                              Hexahistidines are very common tags used in the affinity
15  (YARKARRQARR) at the amino-terminal end and hexahistidine at the carboxy-terminal end to generate CP
16 ) expression of a f310 fusion construct with hexahistidine at the N-terminus of the coding region all
17                         Likewise, pro-sigmaK-hexahistidine chimeras demonstrated that the N-terminal
18 ce (SPR) sensor surface of recombinant human hexahistidine cyclophilin A (His-CypA) is described.
19 alkaline phosphatase was not affected by the hexahistidine epitope tag.
20                                              Hexahistidine epitope tags were used to create aggregati
21                           Both enzymes had a hexahistidine extension at the carboxy-terminal end, use
22  gamma2 subunit containing an amino-terminal hexahistidine-FLAG affinity tag (gamma2HF).
23                                          The hexahistidine-FLAG sequence does not hinder the function
24  immobilized on a FLAG antibody column via a hexahistidine-FLAG-tagged gamma2 subunit, gamma2HF.
25 roduce either the native protein (DapE) or a hexahistidine fusion protein (DapE-His(6)).
26                        We purified FabD as a hexahistidine fusion protein (H6-FabD) and ACP in its na
27 hanced the endocytosis of AcGFP by 150-fold (hexahistidine fusion protein) or 600-fold (decahistidine
28 onsible for this interaction, we constructed hexahistidine fusion proteins from different regions of
29 a and IHFbeta were expressed and purified as hexahistidine fusion proteins, and using electrophoretic
30 d in and purified from E. coli as N-terminal hexahistidine fusion proteins.
31 rio parahaemolyticus, tagged with C-terminal hexahistidine, has been purified to apparent homogeneity
32       Toward this end, we have constructed a hexahistidine (hexa-His)-tagged terminase holoenzyme as
33  Zn(2+) ions binds tightly but reversibly to hexahistidine (His(6)) motifs on surface-exposed protein
34 onal screen utilizes the frequently employed hexahistidine (His(6)) tag as a reporter, and measures i
35                                          The hexahistidine (His(6))/nickel(II)-nitrilotriacetic acid
36  JVZ-007 was initially produced with a c-myc-hexahistidine (his) tag allowing purification and detect
37 over-expressed and purified as an N-terminal hexahistidine ((His)6) tagged fusion containing one zinc
38 its tagged with either hemagglutinin (HA) or hexahistidine (His6) epitopes at the C-terminus.
39                    Here we describe a double-hexahistidine (His6) tag sequence, comprising two hexahi
40 (H)H fragment was equipped with a C-terminal hexahistidine (His6) tether to facilitate the assembly o
41 y fusing the protein with one of eight tags: hexahistidine (His6), thioredoxin (Trx), small ubiquitin
42                                 The purified hexahistidine (His6)-tagged Pseudomonas aeruginosa RhlI
43 mB1 products monitored by anti-MtmB and anti-hexahistidine immunoblotting.
44 ts to the green fluorescent protein (GFP) or hexahistidine in sporulating B. subtilis or in Escherich
45 ell line has been produced that incorporates hexahistidine-labeled p43 into the multisynthetase compl
46 omitans DspB protein engineered to contain a hexahistidine metal-binding site at its C terminus in Es
47   Microbial growth studies indicate that the hexahistidine motif is important for preventing microbia
48 rt that CP binds Zn(II) at this site using a hexahistidine motif, completed by His103 and His105 of t
49                                     Either a hexahistidine or a FLAG octapeptide tag was incorporated
50 the green fluorescent protein AcGFP fused to hexahistidine or decahistidine peptides (3 microM) and N
51                                              Hexahistidine peptides on the engineered MBD1 function a
52                                  The TetA(L)-hexahistidine proteoliposomes exhibit high activities of
53 istidine (His6) tag sequence, comprising two hexahistidines separated by an 11-amino acid spacer, whi
54 nding protein and a polypeptide containing a hexahistidine sequence as the N- and C-exteins, respecti
55                               Inclusion of a hexahistidine sequence permits rapid purification and se
56 binantly engineered to express an N-terminal hexahistidine sequence was expressed from a eukaryotic p
57 des an influenza hemagglutinin epitope and a hexahistidine sequence, permitting sensitive detection a
58 establish that coordination of Ni(II) at the hexahistidine site is thermodynamically preferred over Z
59 II) affinity at a biologically unprecedented hexahistidine site that forms at the S100A8/S100A9 inter
60 -length A. thaliana OEP80 with an N-terminal hexahistidine tag (alphaOEP80(1-732)).
61 h serine and the C terminus was fused with a hexahistidine tag and (ii) this protein was allowed to f
62 hypothesis, TetA(L) has been purified with a hexahistidine tag at its C terminus and reconstituted in
63          The recombinant PauR protein with a hexahistidine tag at its N terminus was purified, and sp
64 dition to the native enzyme, constructs with hexahistidine tag at the amino and carboxyl termini of e
65           Using a soluble form of BAK with a hexahistidine tag at the C terminus and a liposomal syst
66 g in a fusion of vector sequences encoding a hexahistidine tag at the carboxyl terminus.
67                      Recombinant gp65 with a hexahistidine tag at the N terminus or hexahistidine and
68 e expressed proHP14 with a carboxyl-terminal hexahistidine tag in a baculovirus/insect cell system an
69  the full-length BVDV NS5B with a C-terminal hexahistidine tag in Escherichia coli failed due to the
70 imilarly, full-length PatS with a C-terminal hexahistidine tag inhibited heterocyst formation.
71 hat recombinant, purified ICP47 containing a hexahistidine tag inhibits peptide import into microsome
72 lished using a plasmid carrying abgAB with a hexahistidine tag on the carboxyl terminus of AbgB and s
73 hip, or noncovalently bound via a C-terminal hexahistidine tag on the protein to Ni(2+)nitrilotriacet
74 e factor ectodomain via the engineering of a hexahistidine tag onto its C-terminus and its use in com
75 gs show that the catalytic properties of the hexahistidine tag should be taken into consideration whe
76                                            A hexahistidine tag was included at the amino terminus of
77             MsbA modified with an N-terminal hexahistidine tag was overexpressed, solubilized with a
78 combinant PRG B protein (r-PRG B) fused to a hexahistidine tag was purified and analyzed for structur
79 d 277 (following the COOH-terminal 271 and a hexahistidine tag).
80 s a recombinant protein (r-NTP) containing a hexahistidine tag, and refolded to the native structure
81 e human enzyme was cloned with an N-terminal hexahistidine tag, expressed, and purified from a bacter
82 mutants with C-terminal deletions fused to a hexahistidine tag, we determined that the processing sit
83 t human ACAT-1 protein bearing an N-terminal hexahistidine tag.
84 and possesses Mn2+-dependent activity with a hexahistidine tag.
85 nity chromatography using a carboxy-terminal hexahistidine tag.
86 38 MAPKalpha is facilitated by an N-terminal hexahistidine tag.
87 gth recombinant hTF containing an N-terminal hexahistidine tag.
88                                 A C-terminal hexahistidine-tag (C-His) was ligated to the alpha-isofo
89           In this study, the lipA gene and a hexahistidine tagged lipA construct (LipA-His) were over
90                                  Recombinant hexahistidine tagged MmDjC7 (25 kDa) was efficiently exp
91 us solution by electrostatic coupling of the hexahistidine tagged OPH (His6-OPH) and poly(ethylene gl
92 bacterial expression system for a C-terminal hexahistidine tagged version of the native enzyme, which
93                                          The hexahistidine-tagged AcrD protein was purified and recon
94                                              Hexahistidine-tagged alpha and beta apo-subunits were ex
95 garose column was dependent on expression of hexahistidine-tagged alpha(i) and resulted in purificati
96 eterotrimeric G proteins were expressed with hexahistidine-tagged alpha(i) in insect cells, a heterot
97 to the medium can block lysis by a T protein hexahistidine-tagged at its C-terminus, suggesting that
98                                  Recombinant hexahistidine-tagged bovine A1 adenosine receptors were
99 Ni(2+)-NTA modified lipid capable of binding hexahistidine-tagged Cdc42.
100 displacement from inside-out vesicles by the hexahistidine-tagged cytoplasmic domain of band 3, cdb3-
101 an plasminogen was expressed in E. coli as a hexahistidine-tagged fusion protein and chromatographica
102 ssed and purified from Escherichia coli as a hexahistidine-tagged fusion protein.
103 ytic site, have been expressed as individual hexahistidine-tagged fusion proteins in the baculovirus
104 ds displaying chelated nickel bound purified hexahistidine-tagged G protein heterotrimers and, subseq
105 e-tagged green fluorescent protein (GFP) and hexahistidine-tagged G proteins.
106 r could be assembled with partially purified hexahistidine-tagged gamma(2) in vitro to form a functio
107 derivatized to carry chelated nickel to bind hexahistidine-tagged green fluorescent protein (GFP) and
108                  In this study, a C-terminal hexahistidine-tagged helicase domain of the HCV NS3 prot
109                                Recombinant N-hexahistidine-tagged HepK (H6HepK), the cytoplasmic port
110 in, we purified and characterized C-terminal hexahistidine-tagged human CLN2p/tripeptidyl-peptidase I
111 ted the suitability of applying C-terminally hexahistidine-tagged interleukin-12 (IL-12) alpha- and b
112 ic acid (NTA)-coordinated metals avidly bind hexahistidine-tagged macromolecules, including peptides
113                                            A hexahistidine-tagged Methanosarcina barkeri mtmB1 gene,
114                 The crystal structure of the hexahistidine-tagged mouse recombinant catalytic subunit
115                                An N-terminal hexahistidine-tagged MutL was constructed which was acti
116 es were isolated from PS120 cells expressing hexahistidine-tagged NHERF-1 and NHE3 using nickel-NTA-a
117             Gel shift analysis with purified hexahistidine-tagged or native NanR detected three retar
118                          Purification of the hexahistidine-tagged PrnB yields homogeneous protein tha
119 ophic yeast Pichia pastoris and purified the hexahistidine-tagged protein by immobilized metal affini
120                 TviC, purified as C-terminal hexahistidine-tagged protein, shows UDP-GlcNAcA 4-epimer
121 l describes a method for capture of secreted hexahistidine-tagged proteins using expanded-bed adsorpt
122 ilotriacetic acid lipid analog that can bind hexahistidine-tagged proteins, BAK oligomers were formed
123 -five site-specific mutants were produced as hexahistidine-tagged proteins, purified, and examined fo
124 that could be used as a general protocol for hexahistidine-tagged proteins.
125 cetate ligand was immobilized for binding of hexahistidine-tagged red-fluorescing TagRFP, while an ap
126                                     Purified hexahistidine-tagged RpoD migrates at approximately 70 k
127 y plates were used for purifying recombinant hexahistidine-tagged Triticum aestivum (wheat) chlorophy
128 nditions to capture proteins conjugated with hexahistidine-tagged ubiquitin.
129                                            A hexahistidine-tagged variant of dsc19CfaE formed soluble
130 (called aasS) encodes a protein of 60 kDa, a hexahistidine-tagged version of which was readily expres
131                                          The hexahistidine-tagged-packaging proteins were purified to
132                                        Using hexahistidine tags placed at the respective ends of the
133 ides a simple approach to exposing concealed hexahistidine tags while retaining native noncovalent pr
134  both with and without sequences encoding 3'-hexahistidine tags.
135 e was fused to the amino terminus, and (3) a hexahistidine tail was added to the carboxyl terminus.
136                         The FLAG epitope and hexahistidine tail were added to facilitate purification
137 inding protein (PBP) tagged by an N-terminal hexahistidine tail which was immobilized onto Co(2+)-tet

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