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Kloning Fragmen DNA Pengkode Integrase (int) HIV (Human Immunodeficiency Virus) 1 pada Escherichia Coli JM109

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Human Immunodeficiency Virus (HIV) is an RNA virus. It is a lentivirus, a retrovirus member family which causes Acquired Immunodeficiency Syndrome (AIDS). An early event in every retroviral multiplication is the integration of the viral double-stranded DNA genome into the host chromosome. The integration is facilitated by the activation of integrase.The goal of this research is to obtain the HIV integrase encoding gene.

The obtained integrase ORF was intended to be cloned into cloning vector pJETclone and to transform Escherichia coli JM109. The cDNA synthesis was conducted by reverse transcription by converting the RNA genome to DNA. The obtained cDNA was amplified by Polymerase Chain Reaction (PCR) technique to obtain integrase encoding gene. The PCR product was inserted into the plasmid using blunt ended cloning system and was characterized using DNA gel electrophoresis and nucleotide analysis. The DNA gel electrophoresis of PCR product showed the expected band. Further characterization was conducted using nucleotide sequencing showed that the PCR product was homologue to HIV-1 integrase from Indonesia. The PCR was performed on the cloned showed DNA insert on expected size. The nucleotide analysis was conducted on the pure recombinant plasmid, the DNA was read properly.

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Ketersediaan

Informasi Detail

Judul Seri

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No. Panggil

Jurnal Biotek Medisiana Indonesia, 2(2)2013: 59-65

Penerbit

Jakarta : Pusat Biomedis dan Teknologi Dasar Kesehatan., 2013

Deskripsi Fisik

Jurnal Biotek Medisiana Indonesia

Bahasa

ISBN/ISSN

2301-5810

Klasifikasi

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Tipe Isi

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Tipe Media

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Tipe Pembawa

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Edisi

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Subjek

dna
hiv-1

Info Detail Spesifik

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Pernyataan Tanggungjawab

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Versi lain/terkait

Lampiran Berkas

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