Saito, H., Okud, M., Terada, T., Sasaki, S. and Inui, K. (1995) Cloning and characterization of a rat H+/peptide cotransporter mediating absorption of beta-lactam antibiotics in the intestine and kidney. Journal of Pharmacology and Experimental Therapeutics, 275, 1631-1637.

has been cited by the following article:

• TITLE: Preparation of a polyclonal antibody against immunogenic fragment of bovine intestinal peptide transporter I (bPepTI)

  AUTHORS: Xiuxin Zhao, Xueyan Lin, Guimei Liu, Zhonghua Wang

  KEYWORDS: Bovine Type I Peptide Transporter; Clone; Prokaryotes Expression; Antibody Preparation

  JOURNAL NAME: Advances in Bioscience and Biotechnology, Vol.3 No.2, April 18, 2012

  ABSTRACT: The goal of the current study is to prepare polyclonal antibody against bovine intestinal peptide transporter I (bPepTI) in order to develop assay for immunological assessment of protein levels. Antigenicity of the entire bPepTI was analyzed with DNAStar, and a fragment with high antigenicity (bPepTI ORF 1369 - 1695) was selected, cloned in pGEX-6p-1 vector, resulting in a recombinant plasmid GST-BP, which verified by double enzyme digestion and sequenced, the recombinant plasmid was introduced to BL21. Exogenous expression was induced by IPTG and validated by Western blot analysis. The recombinant protein was isolated, purified and used for production of antiserum in mice. The specificity of antiserum was evaluated with immunobloting and titer was estimated with ELISA. Results indicate that the antibody against bPepTI was produced. The optimal GST-BP antigen embedding concentration was 0.5 μg/ml. The optimal dilution was 1:400. An indirect ELISA assay indicates the effective dilution was 1:102400.