Isolation and sequencing of insulin-like growth factor 1 (IGF-1) from Egyptian buffalo via RT-PCR [electronic resource].

By: Contributor(s): Language: English Summary language: Arabic Description: p.19-28Other title:
  • فصل واجراء تسلسل لعامل النمو شبيه الإنسيولين -1 من البقر المصرى باستخدام تفاعل البلمرة العكسى [Added title page title]
Uniform titles:
  • Arab journal of biotechnology, 2008 v. 11 (1) [electronic resource]:
Subject(s): Online resources: In: Arab Journal of Biotechnology 2008.v.11(1)Summary: Insulin-like growth factor 1 (IGF 1) is a member of a heterogeneous group of peptides with important growth-promoting effects in vitro as well as in vivo. It plays a fundamental role in postnatal mammalian growth as a major mediator through which growth hormone exerts its biological effects. We report the isolation and sequencing of full-length IGF-1 cDNA from bovine liver, encoding the IGF-1 protein. RT-PCR reaction was performed in which gene-specific primers corresponding to IGF-1 were utilised employing Pfu, a proof reading and high-fidelity thermostable DNA polymerase. A PCR product of 543 bp, including the open reading frame of IGF-1 gene corresponding to the expected theoretical product size, was successfully amplified. Sequencing of the purified PCR product and its double alignment against a previously known bovine gene identified it as a cDNA corresponding to IGF-1 with the open reading frame encoding the entire IGF-1 precursor of 154 amino acids.
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Insulin-like growth factor 1 (IGF 1) is a member of a heterogeneous group of peptides with important growth-promoting effects in vitro as well as in vivo. It plays a fundamental role in postnatal mammalian growth as a major mediator through which growth hormone exerts its biological effects. We report the isolation and sequencing of full-length IGF-1 cDNA from bovine liver, encoding the IGF-1 protein. RT-PCR reaction was performed in which gene-specific primers corresponding to IGF-1 were utilised employing Pfu, a proof reading and high-fidelity thermostable DNA polymerase. A PCR product of 543 bp, including the open reading frame of IGF-1 gene corresponding to the expected theoretical product size, was successfully amplified. Sequencing of the purified PCR product and its double alignment against a previously known bovine gene identified it as a cDNA corresponding to IGF-1 with the open reading frame encoding the entire IGF-1 precursor of 154 amino acids.

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