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Polymerase chain reaction product

Schwartz, H. E., Ulfelder, K., Sunzeri, F. J., Busch, M. R, and Brownlee, R. G., Analysis of DNA restriction fragments and polymerase chain reaction products towards detection of the AIDS (HIV-1) virus in blood, /. Chromatogr., 559, 267, 1991. [Pg.420]

Cuypers, H. T. M etal. (1992). Storage conditions of blood samples and primer selection affect the yield of cDNA polymerase chain reaction products of hepatitis C virus. J. Clin. Microbiol 30, 3220-3224. [Pg.232]

Hurst, G. Doktycz, M. Vass, A. Buchanan, M. Detection of bacterial DNA polymerase chain reaction products by matrix assisted laser desorption/ionization mass spectrometry. Rapid. Commun. Mass Spectrom. 1996,10,377-382. [Pg.35]

Krahmer, M. T. Johnson, Y. A. Walters, J. J. Fox, K. F. Fox, A. Nagpal, M. Electrospray quadrupole mass spectrometry analysis of model oligonucleotides and polymerase chain reaction products determination of base substitutions, nucleotide additions/deletions, and chemical modifications. Anal. Chem. 1999, 71, 2893-2900. [Pg.35]

Naito, Y. Ishikawa, K. Koga, Y. Tsuneyoshi, T. Terunuma, H. Arakawa, R. Molecular mass measurement of polymerase chain reaction products amplified from human blood DNA by electrospray ionization mass spectrometry. Rapid Commun. Mass Spectrom. 1995,9,1484-1486. [Pg.35]

Wunschel, D. S. Pasa-Tolic, L. Feng, B. B. Smith, R. D. Electrospray ionization Fourier transform ion cyclotron resonance analysis of large polymerase chain reaction products. J. Am. Soc. Mass Spectrom. 2000,11, 333-337. [Pg.35]

Fox, A. Fox, K. F. Castanha, E. Muhammad, W. T. Mass spectrometry polymerase chain reaction products. In Encylopedia of Analytical Science. Amsterdam Elsevier, 2004. [Pg.36]

Hurst, G. B. Weaver, K. Doktycz, M. I Buchanan, M. V. Costello, A. M. Lidstrom, M. E. MALDI-TOF analysis of polymerase chain reaction products from methan-otrophic bacteria. Anal. Chem. 1998, 70, 2693-2698. [Pg.148]

Fig. 19.1 Differential displays comparing RNAs from saline (S)-, imipramine (I)- or fluoxetine (F)-treated rats. Total RNA was extracted from hypothalami of animals treated with the different drugs for two months. Autoradiograms of amplified -[35S]-dATP-labeled PCR (polymerase chain reaction) products after electrophoresis in 6% polyacrylamide gels are shown for two different primer combinations that identified one upregulated (arrowhead) and one downregulated (arrow) fragment in the groups treated with antidepressants (from [4] with permission). Fig. 19.1 Differential displays comparing RNAs from saline (S)-, imipramine (I)- or fluoxetine (F)-treated rats. Total RNA was extracted from hypothalami of animals treated with the different drugs for two months. Autoradiograms of amplified -[35S]-dATP-labeled PCR (polymerase chain reaction) products after electrophoresis in 6% polyacrylamide gels are shown for two different primer combinations that identified one upregulated (arrowhead) and one downregulated (arrow) fragment in the groups treated with antidepressants (from [4] with permission).
McWhorter S, Soper SA. Conductivity detection of polymerase chain reaction products separated by micro-reversed-phase liquid chromatography. Journal of Chromatography A 883,1-9, 2000. [Pg.230]

Analysis of polymerase chain reaction-product by capillary electrophoresis with laser-induced fluorescence detection and its application to the diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency. [Pg.9]

Parent, J.L., C. Le Gouill, M. Rola-Pleszczynski, and J Stankova, A highly efficient technique for cloning of refractory DNA fragments and polymerase chain reaction products. Anal Biochem, 1994. 220(2) 426-8. [Pg.60]

M. Galloway and S.A. Soper, Contact conductivity detection of polymerase chain reaction products analyzed by reverse-phase ion pair microcapillary electrochromatography, Electrophoresis, 23 (2002) 3760-3768. M. Masar, M. Dankova, E. Olvecka, A. Stachurova, D. Kaniansky and B. Stanislawski, Determination of free sulfite in wine by zone electrophoresis with isotachophoresis sample pretreatment on a column-coupling chip, J. Chromatogr. A, 1026 (2004) 31-39. [Pg.865]

Sung, W.C., Lee, G.B., Tzeng, C.C., Chen, S.H., Plastic microchip electrophoresis for genetic screening The analysis of polymerase chain reactions products of fragile X (CGG)n alleles. Electrophoresis 2001, 22, 1188-1193. [Pg.463]

Butler JM, McCord BR, Jung JM, Wilson MR, Budowle B, Allen RO (1994) Quantitation of polymerase chain reaction products by capillary electrophoresis using laser fluorescence. J Chromatogr B 658 271-280. [Pg.160]

Lam, C.W. Analysis of polymerase chain reaction products by denaturing high-performance liquid chromatography. Meth. Mol. Biol. 2006, 336, 73-82. [Pg.191]

Holland, P.M. Abramson, R.D. Watson, R. Gelfand, D.H. Detection of specific polymerase chain reaction product by utilizing the 5 to 3 exonuclease activity of Thermus aquaticus. Proc. Natl. Acad. Sci. 1991, 88, 7276-7280. [Pg.2800]

H. Oberacher, W. Parson, G. Holzl, P.J. Oefner, C.G. Huber, Optimized suppression of adducts in polymerase chain reaction products for semi-quantitative SNP genotyping byLC-MS, J. Am. Soc. Mass Spectrom., 15 (2004) 1897. [Pg.596]

D. C. Muddiman, A.P. NuU, J.C. Hannis, Precise mass measurement of a double-stranded 500 base-pair (309 kDa) polymerase chain reaction product by negative ion ESI-FT-ICR-MS, Rapid Commun. Mass Spectrom., 13 (1999) 1201. [Pg.598]

Polymerase Chain Reaction Products Analysis Using Capillary Electroph Mark P. Richards... [Pg.53]

Greiner TC, Raffeld M, Lutz C, Dick F, Jaffe ES. Analysis of T cell receptor-gamma gene rearrangements by denaturing gradient gel electrophoresis of GC-clamped polymerase chain reaction products. Correlation with tumor-specific sequences. Am J Pathol 1995 146 46-55. [Pg.1478]

Suzuki Y, Orita M, Shiraishi M, Hayashi K, Sekiya T. Detection of ras gene mutations in human lung cancers by single-strand conformation polymorphism analysis of polymerase chain reaction products. Oncogene 1990 5 1037-43. [Pg.1481]

Figure 6.18 Resonant SERS-melting profiles of the polymerase chain reaction products for wild type (squares) and AF508 mutation (triangles) using the 1347cm" SERRS band for CyS. A schematic of the dehybridization process of the polymerase chain reaction products is shown. The first derivatives of the melting profiles are shown in the inset. The mutation has a melting potential of-0.44V,... Figure 6.18 Resonant SERS-melting profiles of the polymerase chain reaction products for wild type (squares) and AF508 mutation (triangles) using the 1347cm" SERRS band for CyS. A schematic of the dehybridization process of the polymerase chain reaction products is shown. The first derivatives of the melting profiles are shown in the inset. The mutation has a melting potential of-0.44V,...

See other pages where Polymerase chain reaction product is mentioned: [Pg.6]    [Pg.263]    [Pg.264]    [Pg.380]    [Pg.543]    [Pg.896]    [Pg.366]    [Pg.298]    [Pg.56]   
See also in sourсe #XX -- [ Pg.1415 , Pg.1422 ]

See also in sourсe #XX -- [ Pg.53 ]




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Polymerase chain reaction product detection

Polymerase chain reaction product purification

Polymerase chain reaction product sequencing

Polymerase chain reaction, production

Polymerase chain reaction, production determination

Reaction polymerase

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