کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2079065 | 1545066 | 2006 | 5 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Molecular Cloning, Tissue Distribution, and Expression in Engineered Cells of Human Orphan Receptor GPR81
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موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
بیوتکنولوژی یا زیستفناوری
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: Molecular Cloning, Tissue Distribution, and Expression in Engineered Cells of Human Orphan Receptor GPR81 Molecular Cloning, Tissue Distribution, and Expression in Engineered Cells of Human Orphan Receptor GPR81](/preview/png/2079065.png)
چکیده انگلیسی
GPR81 was amplified by polymerase chain reaction (PCR) using human fetus kidney cDNA and whole blood genome DNA as template, respectively. The expression profile of GPR81 in human fetus was analyzed by RT-PCR and the result indicated that GPR81 mRNA was most abundant in fetus liver and heart. In addition, the deduced amino acid of GPR81 was compared with the other related molecules by Clustal w/x software, and a molecular phylogenetic tree was constructed with Treeview software. It showed that GPR81 had the highest homology with nicotinic acid receptor in amino acids. After sequence identification, GPR81 was inserted into the plasmid pcDNA3.1(-)/his-mycA and then transfected into Chinese hamster ovary cell (CHO-K1). With the selection of G418, an engineered cell line, which could stably express GPR81, was obtained by the indication of RT-PCR and Western-blot detection. The establishment of the cell line will serve as a means for the further study of GPR81.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chinese Journal of Biotechnology - Volume 22, Issue 3, May 2006, Pages 408-412
Journal: Chinese Journal of Biotechnology - Volume 22, Issue 3, May 2006, Pages 408-412
نویسندگان
WU Fang-Ming, HUANG Huo-Gao, HU Ming, GAO Yue, LIU Yong-Xue,