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1 f bovine insulin was also investigated using cyanogen.
2 cyanide formed after enzymatic hydrolysis of cyanogens.
3 o investigated for maximum recovery of total cyanogens.
4 n used in transgenic cassava to reduce toxic cyanogens.
5             Trace organic species, including cyanogen and ethane, were found in surface measurements.
6                                      Because cyanogens and minor metabolites of cyanide have not indu
7 verted to covalent links by ethanedinitrile (cyanogen) and identified using mass spectrometry.
8 0)), and three were generated against larger cyanogen bromide (A) alpha chain derivatives with each e
9 ed metabolites including the natural product cyanogen bromide (BrCN), which exhibits pronounced allel
10 on of oligodeoxyribonucleotides (ODNs) using cyanogen bromide (BrCN).
11                         Electrophoresis of a cyanogen bromide (CNBr) (CB) digest of sternal cartilage
12                We have previously shown that cyanogen bromide (CNBr) cleavage of cornified envelopes
13 chemokine were identified by MALDI-MS of its cyanogen bromide (CNBr) cleavage products.
14  homogenized in formic acid and subjected to cyanogen bromide (CNBr) cleavage, and the pattern of che
15 n bodies and releasing the target protein by cyanogen bromide (CNBr) cleavage; (ii) determination of
16 is, mass spectral analysis of the C-terminal cyanogen bromide (CNBr) fragment, and comparison of reco
17                                              Cyanogen bromide (CNBr) is a common chemical used to hyd
18 raphy or SDS-PAGE followed by digestion with cyanogen bromide (CNBr) or trypsin.
19  First, ADH was bound to GAMP activated with cyanogen bromide (CNBr) or with 1-cyano-4(dimethylamino)
20 toxified polysaccharides were activated with cyanogen bromide (CNBr) or with 1-cyano-4-dimethylaminop
21  residues, overlapping tryptic peptides, and cyanogen bromide (CNBr) peptides.
22 abeled sigma-1 receptor using Endo Lys C and cyanogen bromide (CNBr) revealed that the [ (125)I]-N-IA
23 rypsin fragments and further localized using cyanogen bromide (CNBr), which hydrolyzes proteins on th
24 ligand and L-tyrosine as the spacer arm to a cyanogen bromide (CNBr)-activated-Sepharose 4B matrix.
25 ced/alkylated, delipidated, and cleaved with cyanogen bromide (CNBr).
26 palmitoylated alpha-tubulin was cleaved with cyanogen bromide (CNBr).
27 gradient centrifugation and was cleaved with cyanogen bromide (CNBr).
28 specificity, using peptides derived from the cyanogen bromide 11 (CB11) fragment of CII.
29                                              Cyanogen bromide activation was transient relative to ol
30 ase I was immobilized onto agarose beads via cyanogen bromide activation.
31                                              Cyanogen bromide also gives high cleavage yields and int
32 on of full-length aptamer in the presence of cyanogen bromide and a 5.9- to 7.6-fold enhancement in t
33 iments reported here, we cleaved VV ATI with cyanogen bromide and determined that the myristoyl moiet
34 lenediamines via successive cyclization with cyanogen bromide and diazotization in the presence of an
35  addition, these proteins were digested with cyanogen bromide and peptide mapping by LC-MS was establ
36 Edman degradation sequencing of radiolabeled cyanogen bromide and skatole digestion products that wer
37 eatment of the 60 kDa cleavage fragment with cyanogen bromide and subsequent MALDI-TOF analysis of th
38  Cleavage of 2-BDB-TAMP-modified enzyme with cyanogen bromide and subsequent separation of peptides b
39 ent, NTS1 was digested with a combination of cyanogen bromide and trypsin and/or chymotrypsin.
40                                              Cyanogen bromide cleavage analyses of the altered pp60(c
41                                              Cyanogen bromide cleavage analysis suggests that one or
42 ing region from each tubulin was obtained by cyanogen bromide cleavage and identified by mass spectro
43       Mapping of the site of modification by cyanogen bromide cleavage and peptide sequencing has sho
44 ansmembrane 1 was labeled, as established by cyanogen bromide cleavage and separation by gel and/or h
45                                              Cyanogen bromide cleavage demonstrated its covalent atta
46  peptides of InlA-MH(6)-Cws were obtained by cyanogen bromide cleavage followed by purification on a
47 rometry and tandem mass spectrometry) of the cyanogen bromide cleavage fragments of the C26A and C15A
48 dues by endoproteinase Lys-C cleavage and by cyanogen bromide cleavage of another receptor construct
49                                 In addition, cyanogen bromide cleavage of bovine gamma-glutamyl carbo
50                                              Cyanogen bromide cleavage of the 32P-labeled rat PDE4D3
51                                              Cyanogen bromide cleavage of the [125I]IACoc photolabele
52                                              Cyanogen bromide cleavage of the covalently labeled rece
53                                              Cyanogen bromide cleavage of the phosphorylated beta 1 A
54 or 23-mer triphosphorylated RNA, followed by cyanogen bromide cleavage of the photo-linked enzyme, lo
55 mployed here a novel solid-phase approach to cyanogen bromide cleavage of the photolabeled receptor f
56                                              Cyanogen bromide cleavage of the precursor protein, foll
57                                              Cyanogen bromide cleavage of the receptor yielded a majo
58                                              Cyanogen bromide cleavage of this molecule yielded a sin
59                 To examine the bridging, the cyanogen bromide cleavage products of mutacin II and its
60 ced at fixed positions in Sup(1-61) to allow cyanogen bromide cleavage to facilitate subsequent mass
61                  Amino acid sequencing after cyanogen bromide cleavage yielded two sequences that are
62 s achieved by purification, deglycosylation, cyanogen bromide cleavage, and sequencing of labeled wil
63                                        After cyanogen bromide cleavage, His(119) is predicted to be w
64  of several analytical techniques, including cyanogen bromide cleavage, reversed-phase chromatography
65 2 with Met to generate an additional site of cyanogen bromide cleavage, the labeled fragment was redu
66 n comparison to recombinant Tromp1 following cyanogen bromide cleavage, which further confirmed the i
67 ls, with the labeled domain then released by cyanogen bromide cleavage.
68                                 Furthermore, cyanogen bromide cleaved a series of wild type and mutan
69                                              Cyanogen bromide cleaved proHNP-1(20-94) at the fortuito
70 y cross-linked to DNA substrates, to partial cyanogen bromide degradation or trypsin proteolysis in o
71 cation, followed by sequencing of an in situ cyanogen bromide digest of membrane bound Hrp12, yielded
72  Microsequencing of peptide fragments from a cyanogen bromide digest of p78 identified this protein a
73                                              Cyanogen bromide digestion analysis of the cross-linked
74           Mixed peptide sequencing following cyanogen bromide digestion identified the 70-kDa membran
75                                              Cyanogen bromide digestion of p66shc produced a phosphor
76                                              Cyanogen bromide digestion of the covalent TnI-TnC compl
77 uding resistance to proteases, resistance to cyanogen bromide digestion, and an ability to form amylo
78 were analyzed by mass spectrometry following cyanogen bromide digestion, and the identity and relativ
79                                              Cyanogen bromide digestion, immunoaffinity chromatograph
80 nteractions that are sensitive to reduction, cyanogen bromide digestion, or limited acid digestion.
81 try of peptides generated by proteolytic and cyanogen bromide digestion.
82  and subjected matrix fibronectin to acid or cyanogen bromide digestion.
83                                         When cyanogen bromide digests of matrix 125I-fibronectin and
84 peptides resulting from complete tryptic and cyanogen bromide digests of the latent protease chain of
85     During the chromatographic separation of cyanogen bromide digests, observation of the absorbance
86 se F, followed by cyanogen bromide; Route B, cyanogen bromide followed by endo-N-glycosydase F.
87  the cytochrome from wild-type bacteria with cyanogen bromide followed by trypsin were analysed by on
88      The tolerogenic epitope is contained in cyanogen bromide fragment 11 (CB11) and is structurally
89       A change in mobility for an N-terminal cyanogen bromide fragment accompanied disulfide cross-li
90 rine phosphorylation is thought to be in the cyanogen bromide fragment containing residues 2-65.
91 III collagen and 9 peptides derived from the cyanogen bromide fragment of bovine type III collagen, a
92            The labeled domain was within the cyanogen bromide fragment of the receptor including the
93 en localized to arginine residues within the cyanogen bromide fragment-(341-380) that contains the pr
94 tein encoded by this sequence, its predicted cyanogen bromide fragmentation, and calculated isoelectr
95 hod that quickly and reliably identifies the cyanogen bromide fragments and posttranslational modific
96 unique peptide determinants contained within cyanogen bromide fragments CB10 and CB11 showing the sig
97 ed within the negatively charged, C-terminal cyanogen bromide fragments of alpha- and beta-tubulin su
98                           Microsequencing of cyanogen bromide fragments of purified icIL-1RaII provid
99 duct of a single probe molecule with the two cyanogen bromide fragments of the CCK receptor represent
100 hat amino acids within the N- and C-terminal cyanogen bromide fragments of the motor domain formed cr
101 ed to 15 synthetic peptides representing all cyanogen bromide fragments.
102 rformance liquid chromatography, tryptic and cyanogen bromide hydrolysis, amino acid analysis, and ma
103 ed wild-type and methionine mutant DATs with cyanogen bromide identified the sequence between residue
104                                Cleavage with cyanogen bromide is beneficial for analysis of membrane
105                             In one approach, cyanogen bromide is used to cleave relatively large pept
106 n of residues flanking this site followed by cyanogen bromide mapping of the [(125)I]RTI 82-labeled m
107            Using [(32)P]Glc-6-P coupled with cyanogen bromide mapping, we demonstrated that the phosp
108  residues from the C-terminal end within the cyanogen bromide peptide CB6.
109                                            A cyanogen bromide peptide containing Glu-14 allows the ex
110            This region is located within the cyanogen bromide peptide fragment alpha1(I) CB6 and is a
111                                      A large cyanogen bromide peptide was recovered, and its further
112 -terminal amino acid analysis of KAM and its cyanogen bromide peptides firmly correlated its amino ac
113                    Mass spectral analysis of cyanogen bromide peptides has established that the cysti
114                                  Analysis of cyanogen bromide peptides of each 3D preparation showed
115                                          The cyanogen bromide peptides were isolated and characterize
116 d monomeric receptor bands were cleaved with cyanogen bromide to demonstrate that both of the photola
117 ing ligands also accelerated the addition of cyanogen bromide to these complexes but slowed the addit
118 e of OmpA fragments generated by protease or cyanogen bromide treatment and by competitive inhibition
119 -51, but its fragmentation pattern following cyanogen bromide treatment is incompatible with the line
120 using a metal ion affinity column, and after cyanogen bromide treatment, avidin affinity purification
121            These two forms were cleaved with cyanogen bromide, and both yielded 40-kDa fragments that
122  endoproteinase Glu-C, endoproteinase Lys-C, cyanogen bromide, and hydroxylamine were consistent with
123 te to allow selective chemical cleavage with cyanogen bromide, and rHD-5 was used to elicit polyclona
124  isolated from each section and cleaved with cyanogen bromide, and the peptides were separated and an
125 rotein bands were individually digested with cyanogen bromide, and the resulting peptide fragments we
126  beta-tubulin was digested with formic acid, cyanogen bromide, endoproteinase Glu-C, or endoproteinas
127 inea pig sigma-1 receptor with EndoLys-C and cyanogen bromide, the [(125)I]IAF label was identified b
128 ated [(32)P]phosphate-G6Pase intermediate by cyanogen bromide, the [(32)P]phosphate remains bound to
129                       In some experiments, a cyanogen bromide-activated resin column bound with CAT w
130 cid sequence is provided, was crosslinked to cyanogen bromide-activated Sepharose 4B and used to immu
131 lumn (containing the GAATTC motif coupled to cyanogen bromide-activated Sepharose 4B) binds EcoRI in
132 pressor, and Gal4 were chemically coupled to cyanogen bromide-activated Sepharose and the temperature
133                  Incubation of denatured and cyanogen bromide-cleaved type XI collagen with radiolabe
134 consistent with both N-terminal and internal cyanogen bromide-derived amino acid sequence.
135                   Further proteolysis of the cyanogen bromide-generated fragment containing cysteine
136            Amino acid microsequencing of two cyanogen bromide-generated peptide fragments of the 43-k
137 C-18-derivatized silica gel and cleaved with cyanogen bromide.
138 es of gC1(457t),the protein was cleaved with cyanogen bromide.
139 rp leader carrier protein was performed with cyanogen bromide.
140 sequential in-gel digestion with trypsin and cyanogen bromide.
141 ment was generated by chemical cleavage with cyanogen bromide.
142 se C, then endo-N-glycosidase F, followed by cyanogen bromide; Route B, cyanogen bromide followed by
143 elty of this approach is the ease with which cyanogen can be administered to a protein sample and the
144 rmation and decomposition of chloramines and cyanogen chloride (CNCl) were measured for a range of ch
145  dioxide, sulfur dioxide, hydrochloric acid, cyanogen chloride, and hydrogen cyanide in negative pola
146 hylene oxide, sulfur dioxide, acrylonitrile, cyanogen chloride, hydrogen cyanide, acrolein, formaldeh
147 n SH-functional group; CO2, SO2, and perhaps cyanogen [(CN)2] may be present within the surface mater
148                                         When cyanogen concentrations were lower, the resulted cyanide
149                                        Total cyanogen content in plum and almond kernels, as well as
150                                              Cyanogen diluted in argon was reacted with laser ablated
151         A method was developed incorporating cyanogen, enzymatic digestion, one-dimensional gel elect
152 e salt bridge, paired group-specific reagent cyanogen (ethanedinitrile; C(2)N(2)) converts naturally
153        A mild method was developed to remove cyanogens from cassava leaves that involved three consec
154          The traditional method for removing cyanogens from pounded cassava leaves is by boiling in w
155 an API building block, 2-cyanothiazole, from cyanogen gas and a readily available dithiane is reporte
156 hat this work will spark further interest in cyanogen gas as a reactive and cost-effective synthetic
157                                            A cyanogen gas production rate of (1.2 +/- 0.3) x10(26) mo
158 6.45 astronomical units showed emission from cyanogen gas.
159 f a phosphorescence-based sensing system for cyanogen halides.
160 an amalgam dental filling target, react with cyanogen in excess argon during condensation at 4 K to f
161 ves is by boiling in water which removed all cyanogens in 10 min.
162 ollected included urinary thiocyanate (SCN), cyanogens in cassava-based food products, recent history
163 uantification of total cyanogenic compounds (cyanogens) in plants was studied using a novel ninhydrin
164 crease root protein levels result in reduced cyanogen levels in roots.
165                                          The cyanogen-linked proteins were isolated by polyacrylamide
166                      Peptides resulting from cyanogen-mediated intermolecular cross-linking of HEW ly
167 pling reactions involved in the formation of cyanogen (NC-CN) from HCN, 1,3-butadiyne from ethyne (i.
168  Gas-phase reaction between copper vapor and cyanogen (NCCN) clearly gives CuCN (not CuNC).
169 s product, cyanoacetaldehyde), with cyanate, cyanogen, or urea.
170 measuring ROS accumulation in transgenic low-cyanogen plants with and without cyanide complementation
171                          We demonstrate that cyanogens play a central role in cassava nitrogen metabo
172                                              Cyanogen readily permeates cell walls and membranes.
173                  The spatial distribution of cyanogen was considerably more diffuse and extended comp
174 oestrogens, flavonoids, simple phenolics and cyanogens with higher apparent affinities (K(m)) and spe

 
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