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人白介素18受體(IL-18R)elisa試劑盒

參考價 2800
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  • 公司名稱廈門侖昌碩生物科技有限公司
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  • 所  在  地廈門市
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  • 更新時間2020/4/26 16:42:45
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產地 國產 級別 其他
Porcine IL-12Rβ2 gene was cloned from mRNA preparation of mitogen-activated peripheral blood mononuclear cells (PBMCs), and its complete nucleotide sequence was determined. To confirm the biological f
人白介素18受體(IL-18R)elisa試劑盒 產品信息

Porcine IL-12Rβ2 gene was cloned from mRNA preparation of mitogen-activated peripheral blood mononuclear cells (PBMCs), and its complete nucleotide sequence was determined. To confirm the biological function, the entire open reading frame (ORF) was re-cloned into a mammalian expression vector, pcDNA3.1/Zeo(+), at the downstream of CMV promoter, and introduced to a Th1-like human lymphoma cell line, Jurkat E6-1. Antibiotic-resistant cells retaining the expression construct were selected then, isolated by the limiting dilution method. An established clone (10B10) constitutively expressed chimeric IL-12Rs composed of intrinsic (human) β1 and extrinsic (porcine) β2 subunits, and produced interferon (IFN)-γ in response to IL-12 of both species with optimal PHA/PMA stimulation. The production of IFN-γ was observed as early as 42 h after culture and appeared to be dose-dependent within the range between 20 and 2000 pg/ml. Thus, this clone not only reacts with IL-12 of both species but also provides a useful tool for quick and sensitive detection of IL-12 bioactivity.Porcine IL-12Rβ2 gene was cloned from mRNA preparation of mitogen-activated peripheral blood mononuclear cells (PBMCs), and its complete nucleotide sequence was determined. To confirm the biological function, the entire open reading frame (ORF) was re-cloned into a mammalian expression vector, pcDNA3.1/Zeo(+), at the downstream of CMV promoter, and introduced to a Th1-like human lymphoma cell line, Jurkat E6-1. Antibiotic-resistant cells retaining the expression construct were selected then, isolated by the limiting dilution method. An established clone (10B10) constitutively expressed chimeric IL-12Rs composed of intrinsic (human) β1 and extrinsic (porcine) β2 subunits, and produced interferon (IFN)-γ in response to IL-12 of both species with optimal PHA/PMA stimulation. The production of IFN-γ was observed as early as 42 h after culture and appeared to be dose-dependent within the range between 20 and 2000 pg/ml. Thus, this clone not only reacts with IL-12 of both species but also provides a useful tool for quick and sensitive detection of IL-12 bioactivity.

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