Cloning and Sequence Analysis of IFN-Alpha in Gushi Chicken
Qian Guan
Abstract
Qian Guan
Abstract
Genome DNA was extracted and then used to amplificate chicken interferon-alpha gene directly with primers which were designed according to the sequences of chicken Interferon-alpha on the GenBank.Specific fragments were linked to pGEM-T Easy vector,then transformed to competent cells of JM109.By idenfication of plasmid PCR and enzyme digestion,positive strain was sent to Takara for sequencing.The sequencing results showed that we have obtained Interferon-alpha gene of Gushi chicken.The results of homology analysis with other chicken interferon-alpha gene published previously in the GenBank by DNAStar analysis revealed that there was identity of 97.9%at nucleotide homology and that of 96.9% at amino acid homology .
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.
Genome DNA was extracted and then used to amplificate chicken interferon-alpha gene directly with primers which were designed according to the sequences of chicken Interferon-alpha on the GenBank.Specific fragments were linked to pGEM-T Easy vector,then transformed to competent cells of JM109.By idenfication of plasmid PCR and enzyme digestion,positive strain was sent to Takara for sequencing.The sequencing results showed that we have obtained Interferon-alpha gene of Gushi chicken.The results of homology analysis with other chicken interferon-alpha gene published previously in the GenBank by DNAStar analysis revealed that there was identity of 97.9%at nucleotide homology and that of 96.9% at amino acid homology .
Key concepts: GenBank, Biology, Gene, Homology (biology), Cloning (programming), Genetics, Sequence analysis, Alpha interferon