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DTIC ADA203018: Cloning and Expression of Genes for Dengue Virus Ty...
by Defense Technical Information Center
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Using oligodeoxynucleotide primers, we cloned the region
of DEN-2 RNA encoding the structural proteins C, prM (M),
and E glycoprotein. The cDNA clones were completely
sequenced. Using a synthetic primer complementary to the
3'-end of DEN-2 RNA, additional cDNA clones, mapping 3'
to the previously characterized clones, A4 and B2 were
isolated. Genome 'walking' using these cDNA clones as
probes, pPM-F12, pPM-A10, pPM53 were isolated, all
mapping toward the 3'-end of the genome. These cDNA
clones were sequenced. To complete the cDNA cloning of
DEN-2 genome, a novel approach was used which involved
the polymerase chain reaction. Using this approach, the
sequences between nucleotide 9950 and the 3'- terminus
were amplified in a Taq polymerase-catalyzed chain
reaction. The amplified DNA was cloned and sequenced.
Keywords: Dengue, Vaccines, Diagnosis medicine.
Date Published: 2018-02-21 19:55:51
Identifier: DTIC_ADA203018
Item Size: 23879832
Language: english
Media Type: texts
# Topics
DTIC Archive; Padmanabhan, Radha K ; ...
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