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1 med quantitatively in the presence of excess beta-mercaptoethanol.
2 essential amino acids, fetal calf serum, and beta-mercaptoethanol.
3      The enzymatic activity was increased by beta-mercaptoethanol.
4 cles was denatured and reduced with urea and beta-mercaptoethanol.
5 rom the radical scavengers ascorbic acid and beta-mercaptoethanol.
6  the RNeasy Fibrous Tissue Kit combined with beta-mercaptoethanol.
7  biotinylation occurred after treatment with beta-mercaptoethanol.
8 ucted 18:1-NO2 detected by exchange to added beta-mercaptoethanol.
9 the protein was denatured in the presence of beta-mercaptoethanol.
10 zed online with o-phthaldialdehyde (OPA) and beta-mercaptoethanol.
11 ng in air, but not in the presence of 100 mM beta-mercaptoethanol.
12  stable in the presence of heating, SDS, and beta-mercaptoethanol.
13 ester bond by removal with dithiothreitol or beta-mercaptoethanol.
14 r was highly stable and resistant to SDS and beta-mercaptoethanol.
15  were also inhibited by DMSO and reversed by beta-mercaptoethanol.
16 atured by boiling in the presence of SDS and beta-mercaptoethanol.
17 g 6 m guanidine HCl, 8 m urea, 2% SDS, or 5% beta-mercaptoethanol.
18 tigen was denatured by heat or reduced using beta-mercaptoethanol.
19  agents such as 5 mM dithiothreitol or 10 mM beta-mercaptoethanol.
20 and occurred in the presence of an excess of beta-mercaptoethanol.
21 the mercurial inhibition was reversible with beta-mercaptoethanol.
22 onated by DEAE chromatography in 6 M urea/4% beta-mercaptoethanol.
23                       Trapping of 1 by O2 or beta-mercaptoethanol (1 M) does not compete with strand
24 man erythrocytes included: pronase, trypsin, beta-mercaptoethanol (2-ME), and heating to 90 degrees .
25 turation by sodium dodecyl sulfate (SDS) and beta-mercaptoethanol (2ME), suggesting the recognition o
26                     Treatment of DENV-2 with beta-mercaptoethanol abolished binding of Fab 1A5, indic
27 p1 can be released, trapped, and detected as beta-mercaptoethanol adducts by mass spectrometry.
28  eosin-5-maleic acid, and the L-cysteine and beta-mercaptoethanol adducts of EM in aqueous and hydrop
29 curate mass measurement was used to identify beta-mercaptoethanol adducts of sulforaphane that had be
30 reatment of alpha1PI with the reducing agent beta-mercaptoethanol also inhibited binding of trypsin t
31 the thiol-reducing agents dithiothreitol and beta-mercaptoethanol also inhibited high affinity [3H]ry
32  derivatized on-line with o-phthaldialdehyde/beta-mercaptoethanol and automatically transferred to a
33  than 100-fold higher than that observed for beta-mercaptoethanol and cysteine, suggesting that thior
34  derivatized on-line with o-phthaldialdehyde/beta-mercaptoethanol and detected by LIF using the 354 n
35 se signature-events were abolished by 100 mM beta-mercaptoethanol and did not occur in a cysteineless
36                     Data analysis shows that beta-mercaptoethanol and ethanol both interact or bind p
37 ended in 2% sodium ascorbate containing 10mM beta-mercaptoethanol and heated to release the folates.
38  treatment with 2% sodium dodecyl sulfate-1% beta-mercaptoethanol and heating to 100 degrees C for 5
39 th glutathione (GSH), N-acetyl-cysteine, and beta-mercaptoethanol and identified the adducts.
40  with derivatization by o-phthalaldehyde and beta-mercaptoethanol and optically gated capillary elect
41 ysteine, homocysteine, cysteinylglycine, and beta-mercaptoethanol) and human serum albumin.
42 eotides, a reducing agent (dithiothreitol or beta-mercaptoethanol), and Mg2+ and was resistant to inh
43 ed by thiol reagents, including glutathione, beta-mercaptoethanol, and dithiothreitol.
44 mined the solvent effects of a co-substrate, beta-mercaptoethanol, and of a model nonsubstrate, ethan
45 d with proteinase K, boiled in detergent and beta-mercaptoethanol, and subjected to sucrose density g
46 reated with three different reductants (DTT, beta-mercaptoethanol, and TCEP).
47 ative thiols methyl-3-mercaptopropionate and beta-mercaptoethanol are shown to add exclusively and qu
48                                 Dioxygen and beta-mercaptoethanol are unable to compete with loss of
49 n of amino acid derivatives, generated using beta-mercaptoethanol as a nucleophile, was characterized
50  sulfhydryl compounds such as l-cysteine and beta-mercaptoethanol as cosubstrates.
51 bation with sodium-dodecyl-sulfate (SDS) and beta-mercaptoethanol at 50-60 degrees C for >=1 h), foll
52                           Urea, ethanol, and beta mercaptoethanol (beta-ME) were used to evaluate the
53  three reducing agents-dithiothreitol (DTT), beta-mercaptoethanol (beta-MCE), and tris(2-carboxyethyl
54                      These mutants produce a beta-mercaptoethanol (beta-ME) adduct of the 2'-deoxyuri
55 peptide linkage by 1,4-dithiothreitol (DTT), beta-mercaptoethanol (beta-ME) or cysteine at low temper
56       Transient treatment with the reductant beta-mercaptoethanol (beta-ME) was able to partially res
57 ur different photostabilizing agents, namely beta-mercaptoethanol (beta-ME), Trolox (TX), n-propyl ga
58 tivity can be restored by the treatment with beta-mercaptoethanol (beta-ME).
59                           The reducing agent beta-mercaptoethanol (betaME) reversibly decreased the a
60 ed blue-fluorescent state by incubation with beta-mercaptoethanol (betaME).
61 ic circular dichroism spectra of the H93G Mb beta-mercaptoethanol (BME) thiolate adduct reveal a high
62 e-based kinetic studies of the reaction with beta-mercaptoethanol (BME) yielded the second-order rate
63                     In the presence of 30 mM beta-mercaptoethanol (BME), the k(cat) increased to 176
64            Our results show that ethanol and beta-mercaptoethanol both alter the equilibrium distribu
65 d to be co-localized on immunoblots of yeast beta-mercaptoethanol cell wall extracts and cytosolic fr
66 7,8-Dihydrobiopterin and other thiols (E.G., beta-mercaptoethanol, cysteine, and glutathione, with le
67                     Higher concentrations of beta-mercaptoethanol decrease the concentration of the q
68                               We encountered beta-mercaptoethanol-dependent artifact signals in weste
69                               Treatment with beta-mercaptoethanol did not impact the apparent molecul
70                               Three types of beta-mercaptoethanol-dissociable complexes were visualiz
71 g SDS, urea, glycerol, ammonium sulfate, and beta-mercaptoethanol, do not interfere with this method.
72 e protects the enzyme from inactivation, but beta-mercaptoethanol does not, suggesting that the 6 bet
73 e protects the enzyme from inactivation, but beta-mercaptoethanol does not, suggesting that these com
74 he concentration of either dithiothreitol or beta-mercaptoethanol eliminated the background problems
75 identified a new spore protein, ExsM, from a beta-mercaptoethanol extract of B. cereus ATCC 4342 spor
76                The moiety was present in the beta-mercaptoethanol extracts of cell walls from both bl
77    N-acetyl cysteine reacts similarly, while beta-mercaptoethanol gives equal amounts of 1,4 and 1,6
78 n the other hand, neither dithiothreitol nor beta-mercaptoethanol had any effect on the N-SMase, sugg
79 side group, an external thiolate provided by beta-mercaptoethanol has likely been recruited to supply
80 anate from trapping of the intermediate with beta-mercaptoethanol in competition with hydride transfe
81 and thiol reducing agents dithiothreitol and beta-mercaptoethanol inactivated the enzyme.
82                                   Ag(2+) and beta-mercaptoethanol increased while SDS and EDTA inhibi
83 eluted from a phenylarsine oxide matrix with beta-mercaptoethanol indicating that they contain vicina
84 ective than the native protein in preventing beta-mercaptoethanol induced aggregation of insulin.
85    The radical abstracts hydrogen atoms from beta-mercaptoethanol (k = 8.8 +/- 0.5 x 10(6) M(-)(1) s(
86       Low concentrations of the co-substrate beta-mercaptoethanol (Kd = approximately 13 mM) decrease
87 d be rescued from l-Hcy-induced apoptosis by beta-mercaptoethanol medium supplementation that increas
88      A structure with the loop occupied with beta-mercaptoethanol mimics binding of MAs(III).
89  reduction species, as demonstrated with the beta-mercaptoethanol model.
90             Hydrogen atom transfer to 1 from beta-mercaptoethanol occurs exclusively from the alpha-f
91  > Mn2+ > Mg2+; no inhibition was found with beta-mercaptoethanol or dithiothreitol.
92  addition of metal complexing agents such as beta-mercaptoethanol or imidazole to the reaction buffer
93 chains were mixed with 300 x molar excess of beta-mercaptoethanol over the p-hydroxymercuribenzoate g
94 th 10 mM phosphate buffer-1 mM Na2EDTA-47 mM beta-mercaptoethanol, pH 5.85 and then with 10 mM phosph
95        Treatment of the labeled samples with beta-mercaptoethanol prior to SDS-PAGE removed the disul
96 yme preparations, such as dithiothreitol and beta-mercaptoethanol, probably preserve enzyme activity
97 of sodium dodecyl sulfate (SDS, surfactant), beta-mercaptoethanol (reducing agent) or ethylenediamine
98                               Treatment with beta-mercaptoethanol removed all radiolabel.
99        Supplementation of culture media with beta-mercaptoethanol rescues CD98hc-deficient cell survi
100     High molecular mass (>200 kDa), SDS- and beta-mercaptoethanol-resistant Fas aggregates were forme
101          Reduction of this disulfide bond by beta-mercaptoethanol restores activity, indicating that
102 ion of a differentiation protocol containing beta-mercaptoethanol resulted in cells that expressed si
103      Mg(2+), Zn(2+), Cu(2+), K(1+), EDTA and beta-mercaptoethanol resulted in enhanced xylanase activ
104 as partially protected via co-treatment with beta-mercaptoethanol, resulting in reduced disulfide bon
105     Treatment of the Co3+-PEPCK complex with beta-mercaptoethanol results in a loss of cobalt and ful
106                Treatment of the complex with beta-mercaptoethanol results in near quantitative releas
107                           In both instances, beta-mercaptoethanol reversed the inhibitory effects.
108             HIV-uninfected persons generated beta-mercaptoethanol-sensitive and -resistant antibodies
109 ed, and V(H)4 determinants were expressed by beta-mercaptoethanol-sensitive antibodies only; and HIV-
110            Moreover, human UBA3 could form a beta-mercaptoethanol-sensitive conjugate with NEDD8 in t
111                                            A beta-mercaptoethanol-sensitive Ubc9-sentrin conjugate co
112                               Reduction with beta-mercaptoethanol showed that the 70-kDa protein cons
113 ol to 500 mM NaCl, 20 mM Tris (pH 8.4), 2 mM beta-mercaptoethanol significantly enhances dimer format
114           Skim milk with low levels of added beta-mercaptoethanol (SM-ME) and untreated skim milk (SM
115                At physiological pH, zinc and beta-mercaptoethanol stimulated the adenine DNA glycosyl
116             Inhibition by dithiothreitol and beta-mercaptoethanol suggests that intramolecular disulf
117       The active site contains a molecule of beta-mercaptoethanol that is positioned between His-106
118  from 280 to 100 kDa, but in the presence of beta-mercaptoethanol the top of the DSP smear disappeare
119                 After selective elution with beta-mercaptoethanol, the peptides are sequenced using n
120 termediates in the reaction of L-serine with beta-mercaptoethanol, they retain activity in the reacti
121                    Under reducing condition, beta-mercaptoethanol (thiol reducing agent) dissociated
122           The addition of the reducing agent beta-mercaptoethanol to samples prepared from METH-treat
123    The cross-linked complex was treated with beta-mercaptoethanol to transfer the 125I photomoiety fr
124 ould be incubated in 10 mM dithiothreitol or beta-mercaptoethanol until the precipitate is dissolved
125             hE(wt) stored in the presence of beta-mercaptoethanol was covalently modified at three cy
126 ion of the isoindole derivative L-serine-NDA-beta-mercaptoethanol was found to follow pseudo-first or
127  Va, derived from factor V treated with 1 mm beta-mercaptoethanol was inactivated more rapidly than t
128     This new assay uses 1,2-diacetyl benzene/beta-mercaptoethanol, which forms a fluorescent iso-indo
129 ide exchange that leads to the generation of beta-mercaptoethanol, which in turn decouples the conjug
130 n the presence of thiol nucleophiles such as beta-mercaptoethanol, which was used as a model, o-QMs a
131 at the radical abstracts hydrogen atoms from beta-mercaptoethanol with a bimolecular rate constant =
132                                    Replacing beta-mercaptoethanol with dithiothreitol in the loading

 
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