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Agarose gels types

Fig. 5. Thirty-four out of 35 potential apo(a) isoforms, separated by SDS-agarose gel electrophoresis. The photograph represents a composite of two separate gels with the reference mixture (St) and 17 different samples applied to each gel. Samples were selected to represent each of the observed isoforms. Twenty-nine samples had single-handed patterns and five samples had double-banded patterns. The double banded types and every fifth single-handed phenotype are indicated at the bottom of each gel lane. [With permission of Marcovina et al. (M12).]... Fig. 5. Thirty-four out of 35 potential apo(a) isoforms, separated by SDS-agarose gel electrophoresis. The photograph represents a composite of two separate gels with the reference mixture (St) and 17 different samples applied to each gel. Samples were selected to represent each of the observed isoforms. Twenty-nine samples had single-handed patterns and five samples had double-banded patterns. The double banded types and every fifth single-handed phenotype are indicated at the bottom of each gel lane. [With permission of Marcovina et al. (M12).]...
Common separation methods can be divided into chemical and physical routes. Chemical approaches rely on the interaction of the surface of different CNT types with surfactant molecules. Early work has shown that octadecylamine [94] and agarose gel [95] adsorb preferably on semiconducting SWCNTs, while diazonium reagents [96] and DNA [97, 98] show preference with metallic tubes. The assemblies with adsorbed molecular species are considerably larger and heavier than the indi-... [Pg.17]

Fig. 5.2.3 Agarose gel electrophoresis of a normal serum (top) and a serum from a type III dys-lipidemic patient (bottom), including the densitometric analysis of the two lanes (left and right, respectively). The normal serum sample shows an -fraction, which is clearly separated from the pre-/ - and the predominant -fraction. In the serum sample from a type III dyslipidemic patient, the pre-/ - and the -fraction are highly elevated and cannot be separated (therefore termed broad-j5-band), while the -fraction is reduced... Fig. 5.2.3 Agarose gel electrophoresis of a normal serum (top) and a serum from a type III dys-lipidemic patient (bottom), including the densitometric analysis of the two lanes (left and right, respectively). The normal serum sample shows an -fraction, which is clearly separated from the pre-/ - and the predominant -fraction. In the serum sample from a type III dyslipidemic patient, the pre-/ - and the -fraction are highly elevated and cannot be separated (therefore termed broad-j5-band), while the -fraction is reduced...
Agarose (molecular biology grade), ethidium bromide (10 mg/mL in water), DNA size markers (Type VII, Roche Diagnostics, Lewes, UK), and standard equipment for agarose gel electrophoresis (e.g., Horizon 58 apparatus Gibco BRL, Paisley, UK). [Pg.136]

Analyze 5 fA on an agarose gel. Migration of the single-stranded bands relative to the double-stranded products varies with gel type and with the product being amplified. It is not necessary to remove the mineral oil from the tube. [Pg.397]

Of the various support matrices that have been used for IEF, only polyacrylamide and agarose gels have come into widespread use.40 The structural features of these two types of gels are very similar. [Pg.276]


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See also in sourсe #XX -- [ Pg.360 , Pg.363 ]




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