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在大肠杆菌中合成的牛白血病病毒(BLV)蛋白的免疫学特性

Immunological characterization of BLV proteins synthesized in Escherichia coli.

作者信息

Siakkou H, Ulrich R, Uelze A, Möhring R, Rosenthal S

机构信息

Department of Cell Differentiation, Academy of Sciences, Berlin, German Democratic Republic.

出版信息

Acta Virol. 1990 May;34(3):256-62.

PMID:1703391
Abstract

Hybrid proteins composed of beta-galactosidase and polypeptides of the bovine leukaemia virus (BLV) including those of the main core protein p24, the envelope protein gp51 and the transmembrane protein gp30 were produced in Escherichia coli and immunologically characterized. The hybrid proteins were immunologically reactive with sera from cattle naturally infected with BLV, demonstrating a possible use for diagnosis of BLV infection. Detection of antibodies was most sensitive with the p24 derivative.

摘要

由β-半乳糖苷酶与牛白血病病毒(BLV)的多肽组成的杂合蛋白,包括主要核心蛋白p24、包膜蛋白gp51和跨膜蛋白gp30,在大肠杆菌中产生并进行了免疫特性分析。这些杂合蛋白与自然感染BLV的牛血清具有免疫反应性,表明其在诊断BLV感染方面可能具有应用价值。用p24衍生物检测抗体最为敏感。

相似文献

1
Immunological characterization of BLV proteins synthesized in Escherichia coli.在大肠杆菌中合成的牛白血病病毒(BLV)蛋白的免疫学特性
Acta Virol. 1990 May;34(3):256-62.
2
A radioimmunoassay detecting the bovine leukaemia virus transmembrane protein gp30 and anti-gp30 antibodies in the serum of cattle.一种用于检测牛血清中牛白血病病毒跨膜蛋白gp30及抗gp30抗体的放射免疫测定法。
Acta Virol. 1989 Mar;33(2):113-20.
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Identification of an immunodominant region on the isolated bovine leukaemia virus (BLV) major envelope protein gp51 by monoclonal antibodies presumably not exposed during natural BLV infection.通过单克隆抗体鉴定分离出的牛白血病病毒(BLV)主要包膜蛋白gp51上的一个免疫显性区域,该区域在自然BLV感染过程中可能未暴露。
Acta Virol. 1990 May;34(3):246-55.
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Synthesis of bovine leukemia virus antigens in Escherichia coli.
Arch Exp Veterinarmed. 1990;44(6):909-16.
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Mapping of sequential epitopes recognized by monoclonal antibodies on the bovine leukaemia virus external glycoproteins expressed in Escherichia coli by means of antipeptide antibodies.借助抗肽抗体鉴定在大肠杆菌中表达的牛白血病病毒外膜糖蛋白上单克隆抗体识别的连续表位图谱。
J Gen Virol. 1992 Sep;73 ( Pt 9):2457-61. doi: 10.1099/0022-1317-73-9-2457.
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Expression of bovine leukemia virus protein p24 in Escherichia coli and its use in the immunoblotting assay.牛白血病病毒蛋白p24在大肠杆菌中的表达及其在免疫印迹分析中的应用。
Acta Biochim Pol. 2001;48(1):227-32.
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Expression of a bovine leukaemia virus envelope fusion protein in E. coli.
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Development of a specific serological test and an efficient subunit vaccine to control bovine leukemia virus infection.开发一种特异性血清学检测方法和一种有效的亚单位疫苗以控制牛白血病病毒感染。
Dev Biol Stand. 1990;72:81-90.
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Antibody production against BLV-p24 in calves following application of cell extracts from tumorous lymph nodes of cattle with enzootic bovine leukosis.应用患地方流行性牛白血病的牛的肿瘤性淋巴结细胞提取物后,犊牛体内针对牛白血病病毒p24的抗体产生情况。
Acta Virol. 1988 Mar;32(2):104-8.
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Polyclonal bovine sera but not virus-neutralizing monoclonal antibodies block bovine leukemia virus (BLV) gp51 binding to recombinant BLV receptor BLVRcp1.多克隆牛血清而非病毒中和单克隆抗体可阻断牛白血病病毒(BLV)糖蛋白51(gp51)与重组牛白血病病毒受体BLVRcp1的结合。
J Virol. 1997 Apr;71(4):3263-7. doi: 10.1128/JVI.71.4.3263-3267.1997.

引用本文的文献

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Expression of the bovine leukemia virus envelope glycoprotein (gp51) by recombinant baculovirus and its use in an enzyme-linked immunosorbent assay.重组杆状病毒表达牛白血病病毒包膜糖蛋白(gp51)及其在酶联免疫吸附测定中的应用。
Clin Diagn Lab Immunol. 2004 Jan;11(1):147-51. doi: 10.1128/cdli.11.1.147-151.2004.
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Fine mapping of HIV-1 Nef-epitopes by monoclonal antibodies.利用单克隆抗体对HIV-1 Nef表位进行精细定位
Arch Virol. 1993;128(1-2):81-95. doi: 10.1007/BF01309790.