Cloning and Sequence Analysis of B2L Gene of Orf Virus Isolated from Jilin Province
Huyan Han
Abstract
Huyan Han
Abstract
According to the DNA sequence of Orf virus which was published on Genbank,two pairs of primers have been designed to amplify B2L gene of JS04 by PCR.The amplified production was combined with pMD19-T vector,then was transformed into DH5.Positive clones identified correctly were sequenced.The length of B2L gene was 1137bp,and the corresponding amino acid sequence was conducted.Sequence analysis showed that the B2L gene homology among ORFNZ2,Shanhjahnpur82/04 strains was 97.8%~ 99.5%.The amino acid sequence homology was 97.6%~ 99.5%.The analysis result of phylogenetic tree showed that the B2L gene.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
According to the DNA sequence of Orf virus which was published on Genbank,two pairs of primers have been designed to amplify B2L gene of JS04 by PCR.The amplified production was combined with pMD19-T vector,then was transformed into DH5.Positive clones identified correctly were sequenced.The length of B2L gene was 1137bp,and the corresponding amino acid sequence was conducted.Sequence analysis showed that the B2L gene homology among ORFNZ2,Shanhjahnpur82/04 strains was 97.8%~ 99.5%.The amino acid sequence homology was 97.6%~ 99.5%.The analysis result of phylogenetic tree showed that the B2L gene.
Key concepts: GenBank, Gene, Phylogenetic tree, Sequence analysis, Biology, Genetics, Homology (biology), Cloning (programming)