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Solid phase sequencer

B5. Berg, C., Hedrum, A., Holmberg, A., Ponten, F., Uhler, M. et al., Direct solid-phase sequence analysis of the human p53 gene by use of multiplex polymerase chain reaction and alpha-thiotriphosphate nucleotides. Clin. Chem. (Winston-Salem, N.C.) 41, 1461-1466 (1995). [Pg.34]

Hultman, T., Stahl, S., Hornes, E., and Chlen, M. (1989) Direct solid phase sequencing of genomic and plasmid DNA using magnetic beads as solid support. Nucleic Acids Res. 17,4937—4946. [Pg.373]

This category represents the most popular subclass of cyclative cleavage reactions. There are many solid-phase sequences with resin attachment via carboxylic acids, followed by elaboration to a free amine five centers away... [Pg.416]

Millipore Australia for support of our solid-phase sequencing program. This work summarises recent work in our group and elements of it (including Fig.l A and C) have been published previously [8]. [Pg.90]

R. Aebersold, G.D. Pipes, R.E. Wettenhall, H. Nika, and L.E. Hood. 1990. Covalent attachment of peptides for high sensitivity solid-phase sequence analysis Ana/. Biochem. 187 56-65. (PubMed)... [Pg.192]

The primary amino acid sequence of polypeptide is routinely determined using the commercially available gas-liquid-phase sequencers [1, 2] and solid-phase sequencers [3, 4] based on the Mman degradation chemistry [.5j. These instruments can routinely obtain the primary amino acid sequence from 10 to 100 pmol of polypeptide. However, the need for higher sequencing sensitivity remains, as Kent et al. [6] have pointed out that rare proteins may only be present at the 30-300 fmol level on 2D-polyacrylamide gels. [Pg.3]

Solid-phase sequencer, an apparatus for peptide/protein sequence analysis. Automated primary structure determination of peptides and proteins using the solid-phase sequencing method is based on cova-... [Pg.349]

In 1973, Wachter and Machleidt (Wachter et a/., 1973 Machleidt et a/., 1973) described the use of aminoglass supports, which for the first time permitted solid-phase sequencing of proteins. The supports are prepared by silylating controlled-pore glass beads (e.g.. Corning CPG-10,200-400 mesh) with 3-aminopropyltrimethoxysilane (Wachter et a/., 1973) or iV-(2-amino-ethyl)-3-aminopropyltriethoxysilane (Bridgen, 1975) (see Fig. 8). The resulting... [Pg.276]

The design and construction of the solid-phase peptide sequencer have been discussed in detail (Laursen et ai, 1975). Basically, the instrument consists of a thermostatted reaction column, which holds the resin-bound peptide, and a series of pumps and valves that deliver reagents and solvents to the column. After each cycle, the liberated thiazolinones are collected in a fraction collector. The instrument is fully automatic and completes a cycle in 60-90 min, depending on how it is programmed. Solid-phase sequencers based on the design of Laursen (1971 Laursen et a/., 1975) are available from Sequemat, Inc. (Watertown, Massachusetts), LKB Instruments (Rockville, Maryland), and Rank-Hilger (United Kingdom). [Pg.278]

Solid-phase sequencing has great potential for microsequencing, especially of hydrophobic polypeptides. Since the peptide is covalently bound, me-... [Pg.280]

In the future, the technique of solid-phase sequencing will be most aided by improved peptide coupling methods and a reduction in the side reactions of the Edman degradation. [Pg.281]

Chapter 6 Solid-Phase Sequencing of Peptides and Proteins... [Pg.326]


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Peptides solid-phase sequencing

Phase sequence

Protein sequencing solid phase

SOLID-PHASE SYNTHESIS OF SEQUENCE-SPECIFIC PHENYLACETYLENE OLIGOMERS

Solid-phase sequencing

Solid-phase sequencing

Solid-phase sequencing of peptides and proteins

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