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Poly synthetase molecular weight

Table 1 is a summary of the amino acid composition of poly(ADP-ribose) synthetase. It reveals that the enzyme consists of 1,014 amino acid residues with a calculated molecular weight of 113,153. The total amino acid composition calculated from the deduced amino acid sequence coincided well with that determined experimentally. [Pg.490]

Fig. 1. Estimation of the size of mRNA for bovine poly(ADP-ribose) synthetase by in vitro translation of size fractionated poly (A) + RNA and Northern blot analysis. A. Size-fractionation of poly (A) + RNA and location of mRNA for the enzyme. Bovine thymus poly(A)+ RNA was size-fractionated by neutral sucrose density gradient centrifugation and RNA in each fraction was translated in vitro. The translated products were immunoprecipitated, and separated on a 7.5% SDS-polyacrylamide gel. B. Typical fluorogram of the gel. Lanes 1, 2, 3, 4, and 5, correspond to fractions 1, 3, 5, 7, and 9, respectively. Molecular weight markers a, p-galactosidase (116K), b, phosphorylase a(95K), c, bovine serum albumin (68K), d, ovalbumin (43K), e, lysozyme (14.3K). C. Northern blot analysis of bovine thymus poly(A)+ RNA. RNA (2 pg per lane) was separated on a 1.2% agarose/formaldehyde gel, transferred to a nitrocellulose filter, and hybridized with the p-iabelled 2.7 kb insert cDNA prepared from the clone ARS-1. Size markers used were 28 S(4.9 kb), 18 S(2.0 kb)rRNA, 3.8 kb, 2.7 kb, and 1.1 kb denatured DNA. Reprinted from Taniguchi etaL, Eur J Biochem 171 571-575,1988. Fig. 1. Estimation of the size of mRNA for bovine poly(ADP-ribose) synthetase by in vitro translation of size fractionated poly (A) + RNA and Northern blot analysis. A. Size-fractionation of poly (A) + RNA and location of mRNA for the enzyme. Bovine thymus poly(A)+ RNA was size-fractionated by neutral sucrose density gradient centrifugation and RNA in each fraction was translated in vitro. The translated products were immunoprecipitated, and separated on a 7.5% SDS-polyacrylamide gel. B. Typical fluorogram of the gel. Lanes 1, 2, 3, 4, and 5, correspond to fractions 1, 3, 5, 7, and 9, respectively. Molecular weight markers a, p-galactosidase (116K), b, phosphorylase a(95K), c, bovine serum albumin (68K), d, ovalbumin (43K), e, lysozyme (14.3K). C. Northern blot analysis of bovine thymus poly(A)+ RNA. RNA (2 pg per lane) was separated on a 1.2% agarose/formaldehyde gel, transferred to a nitrocellulose filter, and hybridized with the p-iabelled 2.7 kb insert cDNA prepared from the clone ARS-1. Size markers used were 28 S(4.9 kb), 18 S(2.0 kb)rRNA, 3.8 kb, 2.7 kb, and 1.1 kb denatured DNA. Reprinted from Taniguchi etaL, Eur J Biochem 171 571-575,1988.

See other pages where Poly synthetase molecular weight is mentioned: [Pg.146]    [Pg.462]    [Pg.243]    [Pg.13]    [Pg.21]    [Pg.29]    [Pg.300]    [Pg.392]    [Pg.47]    [Pg.167]    [Pg.171]    [Pg.517]   
See also in sourсe #XX -- [ Pg.3 , Pg.5 ]




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