Fingerprint analysis

Kramer, A., Vakalopoulou, E Schleuning, W.-D., and Schneider-Mergener, J. (1995) A general route to fingerprint analyses of peptide-antibody interactions using a clustered amino acid peptide library comparison with a phage display library. Mol. Immunol. 32,459 165. 

A hybridization probe is a piece of nucleic acid which can be hybridized to specific target sequences, and which is labelled to allow their detection. A probe may be DNA or RNA, and can be labelled either radioactively or chromogenically. For genetic fingerprint analyses a high activity label is necessary and for this reason we routinely employ 32p rjsia probes. 

Fingerprint analyses Practically all conceivable nucleic acids with altered moieties that form, whether from oxygen stress, aldehydes, or other reactive species, cannot be immediately chemically defined. This is neither practical, nor routinely possible. Most investigators in the field of nucleic... 

McComb, M. Perlman, D.H. Huang, H. CosteUo, C.E. Evaluation of an on-target sample preparation system for matrix-assisted laser desorption/ionization time-of-flight mass spectrometry in conjunction with normal-flow peptide high-performance liquid chromatography for peptide mass fingerprint analyses. Rapid Commun. Mass Spectrom. 2006, 21,44-58. 

A total of 124 of 126 isolates from early- (1-10 days), middle- (11-20 days), late- (21-32 days), and post- (>32 days) fermentations of komesu were the same group of strains that belong to Acetobacter (A.) pasteurianus, and only 2 of the 126 strains that appeared at post-fermentation referred to the same species, but were recognized as a group of strains different from the former group of strains on the basis of DNA fingerprinting analyses (Nanda et al. 2001). A total of 50 strains isolated from the early, middle, and late phases of static kurosu fermentation were identified to be one group of A. pasteurianus (Table 2.1). 

Results of a Fingerprint Analysis of a Masterbatch and Remill Mixing Process of a Styrene-Butadiene Rubber-Carbon Black (SBR-CB) Compound on a CK320E Intermeshing Mixer with PES3 Rotors (Harburg Freudenberger)... 

Fingerprint analysis a direct-injection GC/FID analysis in which the detector output—the chromatogram—is compared to chromatograms of reference materials as an aid to product identification. 

Zabet-Moghaddam, M. et al., Pyridinium-based ionic liquid matrices can improve the identification of proteins by peptide mass-fingerprint analysis with matrix-assisted laser desorption/ionization mass spectrometry. Anal. Bioanal. Chem., 384, 215, 2006. 

The comparison of evidence is a well-established function of the forensic laboratory. Fields of expertise such as document examination, fingerprint analysis, firearms examination, as well as a myriad of other types of examination, all rely on the comparison of an exhibit with either a reference collection or another specific exhibit. 

The University of Manchester Bioinformatics Education and Research site (UMBER). Useful because it is the home of the PRINTS (9,10) resource for protein fingerprint analysis and a valuable teaching site for bioinformatics. 

Stacey, G. N Bolton, B. J., Morgan, D., Clark, S. A., and Doyle, A. (1992) Multilocus DNA fingerprint analysis of cell banks Stability and culture identification in human B lymphoblastoid and mammalian cell stocks. Cytotechnology 8,13-20. 

Van Vendeloo et al. developed a gas chromatographic method for fingerprint analysis of illicit heroin samples, capable of detecting the main components acetyl codeine, caffeine, codeine, heroin, 6-0-monoacetylmorphine, morphine and quinine in one run in 25 min. Heroin, morphine, codeine and caffeine could be quantified directly, 6-0-monoacetylmorphine and acetylcodeine were not fully separated. Quantitation of the latter two required acetylation of 6-0-monoacetylmorphine to heroin. A packed column of 1 % OV-1 on Chromosorb G HP was used... 

Radioiodination of nucleic acid (Fig. 7.22) is one of the earliest, convenient methods to obtain high specificity (Commerford, 1971) but its use has been declining considerably. It might still have some usefulness for in situ hybridization and, in the case of RNA, in two-dimensional fingerprint analysis. One should be aware of the volatile nature of I. The reaction is carried out in two stages (i) nucleic acid (10-1000 (xM as cytosine) is heated to 60°C for about 10 min in the presence of 30-100 p.M radioiodide, TICI3 at 5-10 times... 

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