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1 d with immature HIV-1 particles treated with nonionic detergent.
2  sucrose density gradients and are stable in nonionic detergents.
3 The PDE4D3 form was readily solubilized with nonionic detergents.
4 ivalent ion requirements, effect of salt and nonionic detergents.
5 und proteins is performed in the presence of nonionic detergents.
6  fraction by high salt concentrations, or by nonionic detergents.
7 ssemble from a single-chain galactolipid and nonionic detergents.
8 urea or sodium dodecyl sulfate (SDS) but not nonionic detergents.
9 C-MMOH complex is perturbed by salts but not nonionic detergents.
10 ngth but is nearly unaffected by addition of nonionic detergents.
11 ions of Triton X100, Nonidet P40 and Brij-58 nonionic detergents.
12 n Stat5bA630P in cell extracts prepared with nonionic detergents.
13 egions that are resistant to extraction with nonionic detergents.
14 ies of straight chain anionic, cationic, and nonionic detergents.
15 ains can be extracted differentially by cold nonionic detergents.
16 ere readily dissociable upon the addition of nonionic detergent (0.1% Triton X-100).
17 y pure systems that contain a bile salt or a nonionic detergent, a phosphatidylcholine or a fatty aci
18 nd resistance of E-cadherin to extraction by nonionic detergents, a measure for the association of th
19               Treatment of the extracts with nonionic detergents, a membrane-altering inhibitor of fa
20 cause a fraction of DAH remains insoluble to nonionic detergent along with actin.
21                                              Nonionic detergents alter the Bax conformation to expose
22  measured by resistance to solubilization in nonionic detergent and by copatching with a raft-residen
23 be induced to deflagellate by treatment with nonionic detergent and Ca2+.
24 etermined crystal structure solubilized by a nonionic detergent and complexed with an antibody fragme
25                        The enzyme requires a nonionic detergent and divalent metal ions for activity.
26 scopic scale measured as lower solubility in nonionic detergent and in the microscopic scale evident
27 d was partially released by treatment with a nonionic detergent and reducing agent, consistent with a
28 ion of mature virions after treatment with a nonionic detergent and reducing agent.
29 fied virions occurred after treatment with a nonionic detergent and reducing agent.
30 rmined biochemically using solubilization in nonionic detergents and by confocal microscopy.
31 ter-soluble organic dyes are also soluble in nonionic detergents and can be extracted by adding salt,
32 p235 PI 5-kinase include high sensitivity to nonionic detergents and relative resistance to wortmanni
33  stable at 4 degrees C in buffers containing nonionic detergents and showed a redox midpoint potentia
34 luble molecule to one that aggregated, bound nonionic detergent, and bound to lipid vesicles, propert
35 om up to 1 ml of plasma, gently lysed with a nonionic detergent, and directly amplified.
36 ne tag was overexpressed, solubilized with a nonionic detergent, and purified by nickel affinity chro
37 teria, purified the enzyme in the absence of nonionic detergents, and assayed pregnenolone formation
38 embrane vesicles, it can be solubilized with nonionic detergents, and it shifts from 220 to 200 kDa u
39 ely co-immunoprecipitated with p59(fyn) from nonionic detergent (Brij 96) extracts of early postnatal
40                      It was solubilized in a nonionic detergent buffer, enriched by differential cent
41 hese differences, each mutant was soluble in nonionic detergent but unable to assemble into homomeric
42 ion of the Ca-ATPase into monomers using the nonionic detergent C(12)E(8) gave a pattern of phosphory
43 s (bilayer interfacial area), inclusion of a nonionic detergent (C(12)E(8)), and the presence of chol
44 mild extraction of plasma membranes with the nonionic detergent C12E8 (octaethylene glycol n-dodecyl
45           Treatment of nb/nb ghosts with the nonionic detergent C12E8 (octaethylene glycol n-dodecyl
46           We have studied the effects of the nonionic detergent C12E8 on Ca-ATPase enzymatic activity
47 ive to the presence of contaminants, such as nonionic detergents commonly found in biological samples
48 ich dissociates and loses kinase activity in nonionic detergent conditions.
49 of mannose 6-phosphate or octyl glucoside, a nonionic detergent containing a sugar group, to cocultur
50 viral cores from particles treated with mild nonionic detergent; cores were isolated by sedimentation
51   When fresh erythrocytes are solubilized by nonionic detergent, CR1 partitions to the cytoskeleton f
52  Examination of virions after treatment with nonionic detergent demonstrated that: (i) in extracellul
53 column eluate after displacement of SDS with nonionic detergent, demonstrated by gel filtration and c
54                            It was found that nonionic detergents did not dissociate the polymers, but
55                                          The nonionic detergent, digitonin, and the anionic detergent
56                    A unique combination of a nonionic detergent dodecyl-beta-d-maltopyranoside (DDM)
57 oli and solubilized from cell lysates in the nonionic detergent, dodecyl maltoside.
58      In addition, we establish with both the nonionic detergent dodecylmaltoside and the anionic dete
59                                          The nonionic detergent dodecylmaltoside solubilized function
60 ssed in Sf9 insect cells and stabilized with nonionic detergents during purification.
61 The receptors are resistant to extraction by nonionic detergent even after latrunculin A treatment.
62 brain, it was immunoaffinity-purified from a nonionic detergent extract of washed mouse brain membran
63        Lipid rafts were isolated after cold, nonionic detergent extraction of cells and gradient cent
64                                              Nonionic detergent extraction of cultured epithelial cel
65 urified virions and was largely resistant to nonionic detergent extraction, suggesting a location wit
66 supported monolayers and remains bound after nonionic detergent extraction.
67 oimmunoprecipitates with beta1-integrin from nonionic detergent extracts and colocalizes with vinculi
68                                           In nonionic detergent extracts from MDCK II cells, the tigh
69 gh the extraction of the outer membrane with nonionic detergent followed by ion-exchange chromatograp
70 e-exposure to 4-nonylphenol (4-NP), a common nonionic detergent found in sewage sludge amended soils.
71 ng monospecific anti-IAP100 antibodies and a nonionic detergent-generated chloroplast lysate gave the
72                            In the absence of nonionic detergents, gp140 of the KNH1144 genotype, term
73                                     However, nonionic detergents have been shown to cause signal supp
74 ucrose gradients nor decreased solubility in nonionic detergents-hence it does not promote lipid raft
75 ents or heat but are relatively resistant to nonionic detergents, high salt concentrations, or exposu
76 mplification buffer (vLAB) prepared with the nonionic detergent IGEPAL enables qualitative detection
77 nant by treating the stock suspension with a nonionic detergent, Igepal CA-630.
78 dylinositol 4-kinase (PI 4-K) (stimulated by nonionic detergent, inhibited by adenosine, inhibited by
79 sulted in elevated FAK.Cas complex levels in nonionic detergent-insoluble fractions, indicating incre
80 s, we analyzed whether they partitioned into nonionic detergent-insoluble glycolipid-enriched membran
81 e chain oxidation is observed for TBP when a nonionic detergent is present.
82 ightly membrane bound, and its inhibition by nonionic detergents is described.
83                A detailed list of compatible nonionic detergents is included, along with a protocol f
84 s stimulated to a much greater extent by the nonionic detergent lauryldimethylamine oxide (LDAO) than
85           Additionally, the incorporation of nonionic detergents like poly(ethylene oxide) (PEO) and
86 r to the fidelity when using IN derived from nonionic detergent lysates of HIV-1 virions.
87 he SC-TR assay is compatible with the use of nonionic detergents, making it more versatile than other
88 ganic dyes that uses a reagent composed of a nonionic detergent mixed with an alcohol is described.
89 ively modulating TATA box binding by TBP and nonionic detergent modulating the interdomain interactio
90                                          The nonionic detergent n-dodecyl-beta-D-maltopyranoside is c
91 sozyme treatment and solubilization with the nonionic detergent n-dodecyl-beta-d-maltoside, which pre
92 synaptosomal and microsomal membranes by the nonionic detergent n-octyl- beta-glucopyranoside; the so
93 etergent sodium dodecyl sulfate (SDS) or the nonionic detergent n-octyl-beta-D-glucopyranoside (betaO
94 ted membranes and membranes treated with the nonionic detergent n-octyl-beta-d-glucopyranoside, sugge
95  protein was monodisperse and dimeric in the nonionic detergent n-octyl-beta-D-glucopyranoside.
96  by extracting pig brain microsomes with the nonionic detergent Nonidet P-40 and purified approximate
97 is strongly promoted by molybdate and by the nonionic detergent Nonidet P-40.
98                                    Next, the nonionic detergent, Nonidet P-40, was used to extract th
99       Treatment of intact organisms with the nonionic detergent NP-40 resulted in dissolution of the
100    It was extracted from the membrane by the nonionic detergent NP-40, together with glycerophospholi
101 ffer containing oxidized glutathione and the nonionic detergent octyl glucoside, the G protein regain
102 Escherichia coli polar lipid extract and the nonionic detergent octyl-beta-d-glucopyranoside.
103                                          The nonionic detergent octyl-beta-glucoside, which does not
104                                The effect of nonionic detergents of the n-alkyl-beta-D-glucopyranosid
105 d purified using ionic detergent, LDS-P5, or nonionic detergent, OG-P5.
106                 The effects of the ionic and nonionic detergents on catalytic activity of endometase
107                    Cell extraction with cold nonionic detergents or alkaline carbonate prepares an in
108 f bands around 27 kDa, and extractions using nonionic detergents or high pH conditions demonstrate th
109 hrome c oxidase (CcO), solubilized by either nonionic detergents or phospholipids, completely dimeriz
110 ing a multiwell detergent screening assay, 4 nonionic detergents out of 80 tested were found to dispe
111  and extracted in buffer without or with the nonionic detergent polidocanol.
112                                          The nonionic detergent polyoxyethylene 10 lauryl ether (C12E
113                           On the other hand, nonionic detergents readily induced homodimers and heter
114 ntrolled manner with various combinations of nonionic detergents, reducing agents, and proteolytic en
115 ane-associated Type I ROPs display increased nonionic detergent solubility in pan1 mutants, suggestin
116 a in two distinct intracellular pools (i.e., nonionic detergent-soluble and detergent-insoluble pools
117  in most detergents and can be maintained in nonionic detergent solutions for extended periods of tim
118 eport, we present evidence that NS4A forms a nonionic-detergent-stable complex with the NS4B5A polypr
119 MALDI-TOF can be obtained in the presence of nonionic detergents such as hydrogenated Triton X-100 (R
120 s are characterized by their insolubility in nonionic detergents such as Triton X-100 at 4 degrees C.
121                                              Nonionic detergents such as Triton X-100, Nonidet P-40 a
122 purified virions and could be extracted with nonionic detergent, suggesting membrane insertion.
123                 Caspr is poorly extracted by nonionic detergents, suggesting that it is associated wi
124  the critical micelle concentration (CMC) of nonionic detergents tested.
125  within certain temperature ranges, or other nonionic detergents than bilayers in the fluid phase.
126  by octyl-beta-glucoside, the latter being a nonionic detergent that selectively extracts only band 3
127                                          The nonionic detergents that are typically used to achieve s
128                           In the presence of nonionic detergent, the 6A7 antibody avidly binds the mo
129 ared by freeze-thawing or by the addition of nonionic detergent, the Vn antigen content was drastical
130 uantify the effects that a popular series of nonionic detergents, the n-alkyl-beta-D-glucopyranosides
131                                Addition of a nonionic detergent to CVM caused the average pore size t
132  subfraction of particulate PIKfyve resisted nonionic detergent treatment, implying association with
133 of the membrane by low concentrations of the nonionic detergent Triton X-100 (0.3%) or the mild ionic
134 n the presence of a low concentration of the nonionic detergent Triton X-100, specific pyrethroid bin
135 omplex was not altered by treatment with the nonionic detergent Triton X-100, suggesting a lack of as
136 lyzed by immunostaining with and without the nonionic detergent Triton X-100, using the CD44H monoclo
137 tion of M. tuberculosis H37Ra lysates by the nonionic detergent Triton X-114 revealed the Eis protein
138 strategy based on micelle formation with the nonionic detergent Triton X-114.
139 ified the breakthrough peak to represent the nonionic detergent Triton.
140                                          The nonionic detergents Triton X-100, Nonidet P-40, Brij, Tw
141 ells and was extracted from the membranes by nonionic detergents (Triton X-100, dodecyl maltoside).
142                            The presence of a nonionic detergent, Triton X-100, was found essential to
143            The reaction was inhibited by the nonionic detergent Tween 20, and several lipids did not
144 ERT from porcine brain (pSERT) using a mild, nonionic detergent, utilize fluorescence-detection size-
145 ins extracted from the viral membrane with a nonionic detergent were shown to conserve the a-determin
146 m to which various combinations of ionic and nonionic detergents were admixed.
147                                    Ionic and nonionic detergents were inhibitory for each enzyme.
148  In contrast, Envs solubilized in Cymal-5, a nonionic detergent, were unstable at room temperature, a
149  DeltaE-torsin A were readily solubilized by nonionic detergents, were similarly accessible to protea
150 , Duffy, XK, and Kell readily extractable by nonionic detergent with no effect on the retention of ba
151               We have also found that mixing nonionic detergents with alcohols markedly reduces their
152 e outer membrane complex by a combination of nonionic detergents with reducing agents but not by the

 
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