ratory
band 11, which is a doublet, is partially resolved in UCD 522A. The laboratory
form of band 12 (chromosome IV) is not present. Instead, a faster- migrating
band is seen which just merges with the partially resolved doublet corresponding
to laboratory band 11. The karyotype of the genetically purified and presumably
homozygous clone 522XA (lane D) has a different profile than its progenitor,
UCD 522A. The band migrating just ahead of laboratory band 3 is absent
while laboratory doublet band 11, partially resolved in UCD 522A, is completely
resolved.
The profile of UCD 505K (lane E) indicated the presence of laboratory
band 3, the faster migrating band seen in the UCD 522A profile, and a
unique band migrating between laboratory bands 4 and 5. The faster migrating
form of laboratory band 7 seen in UCD 522A and 522XA has a diffuse counterpart
in UCD 505K profile. Laboratory bands 10, 11, and 13 have approximate
counterparts in UCD 505K, but band 12 is absent.
The profile of UCD 595A (lane F) indicated a very faint counterpart to
laboratory band 1, perhaps three merged bands migrating between laboratory
bands 2 and 3, and a partially resolved doublet corresponding to laboratory
band 5. Laboratory bands 6 through 9 have diffuse and approximate counterparts
in this wine strain which may indicate the presence of additional and
unresolved chromosomes. As in UCD 505K, laboratory bands 10, 11, and 13
have counterparts in this strain, while band 12 is absent. Instead, a
faint band migrates slightly more slowly than the UCD 595A form of laboratory
band 11.
While the electrophoretic profiles of UCD 522A, UCD 505K, and UCD 595A
provide qualitative evidence for aneuploidy, a more useful qu
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Page: All 1 2 3 4 5 6 Related biology technology :1.
DNA/RNA Blotting With the Trans-Blot SD Semi-Dry Electrophoretic Transfer Cell2.
Separation and Comparison of Proteins From Virulent and Nonvirulent Strains of the Fish Pathogen Flavobacterium psychrophilum, Using a 2-D Electrophoretic Approach3.
Saccharomyces cerevisiae4.
Saccharomyces cerevisiae5.
Saccharomyces cerevisiae6.
Saccharomyces cerevisiae7.
Cytosolic expression of Green Fluorescent Protein (GFP) and its derivatives
in the yeast Saccharomyces cerevisiae: Detection in vivo using
the Varian Cary Eclipse8.
Monitoring fluorescence resonance energy transfer (FRET) between GFP
fusions in lysates of the yeast Saccharomyces cerevisiae using the
Varian
Cary Eclipse