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1 ferring glucose to an exogeneous acceptor, n-dodecyl beta-D-maltoside.
2 retention of Ste14p activity occurred with n-dodecyl-beta-d-maltoside.
3 osphocholine, n-decyl-beta-D-maltoside, or n-dodecyl-beta-D-maltoside.
4 llection device as well as the addition of n-Dodecyl beta-d-maltoside (0.01%) in the collection buffe
5 of PSMalpha3 peptides in solution and with n-dodecyl-beta-d-maltoside, a micelle-forming detergent, w
7 gastric H+, K(+)-ATPase was solubilized by n-dodecyl beta-D-maltoside and electrophoresed in blue nat
8 brane channel (Aquaporin-0) solubilized by n-Dodecyl beta-D-Maltoside and from previously published s
9 maintained during membrane solubilization by dodecyl beta-D-maltoside and purification by chromatogra
11 sence of lipids and the common surfactants n-dodecyl-beta-D-maltoside and octyl-D-glucoside, but they
13 membranes were solubilized with 0.1% (w/v) n-dodecyl beta-D-maltoside, and the RC complex was purifie
14 s cultured fibroblasts were solubilized with dodecyl-beta-d-maltoside, and the F(1)F(0) was isolated
16 urified Gt to photoactivated Rho (Rho*) in n-dodecyl beta-D-maltoside (DDM) examined by gel filtratio
18 he modified PDMS with a dynamic coating of n-dodecyl beta-d-maltoside (DDM), which prevents protein s
19 ethylsiloxane) channels using a mixture of n-dodecyl-beta-D-maltoside (DDM) and sodium dodecyl sulfat
20 s provided for the ability of the surfactant dodecyl-beta-D-maltoside (DDM) to prevent charge-induced
21 on surfactants used in structural biology, n-dodecyl-beta-D-maltoside (DDM), but contains a disulfide
24 ontaining membranes were solubilized in 1% N-dodecyl-beta-D-maltoside in the presence of 0.4% sheep b
25 ecting a membrane protein complex within a n-dodecyl-beta-d-maltoside micelle, we demonstrated a powe
26 beta(1)-adrenergic receptor (beta(1)AR) in n-dodecyl-beta-D-maltoside micelles upon titration with tw
27 ionic sodium dodecyl sulfate than in neutral dodecyl-beta-D-maltoside micelles, and TM2 was disordere
28 n techniques in mild detergents, including n-dodecyl-beta-D-maltoside, n-tetradecyl-beta-D-maltoside,
29 n affect the menaquinone binding site, but n-dodecyl beta-D-maltoside preparations exhibit a relative
30 ue native PAGE and FRET assays revealed 1% n-dodecyl beta-d-maltoside-resistant cis-dimerization for
31 demonstrating that in micelles containing n-dodecyl-beta-D-maltoside, Rho exists as a mixture of mon
32 mosynechococcus elongatus via conventional n-dodecyl-beta-D-maltoside solubilization (DM-PSI) and a,
33 Receptors solubilized with the detergent n-dodecyl beta-D-maltoside were found to sediment as a sin
34 solubilization with the nonionic detergent n-dodecyl-beta-d-maltoside, which preserved both hydrophil
35 trifugation of mitochondria solubilized with dodecyl-beta-D-maltoside, with an approximately eightfol