Antigenicity of synthetic peptides 159-169 and 151-169 of Torpedo acetylcholine receptor alpha chain.
作者信息
McCormick D J, Lennon V A, Atassi M Z
出版信息
Biochem J. 1985 Oct 1;231(1):245-6. doi: 10.1042/bj2310245b.
Abstract
摘要
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Antigenicity of synthetic peptides 159-169 and 151-169 of Torpedo acetylcholine receptor alpha chain.电鳐乙酰胆碱受体α链合成肽159 - 169和151 - 169的抗原性
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引用本文的文献
1
Antigenicity of the sequence 152-167 in alpha subunits of Torpedo acetylcholine receptor.电鳐乙酰胆碱受体α亚基中152 - 167序列的抗原性。
Biochem J. 1985 Oct 1;231(1):247. doi: 10.1042/bj2310247.
本文引用的文献
1
Production and assay of antibodies to acetylcholine receptors.乙酰胆碱受体抗体的制备与检测
Methods Enzymol. 1981;74 Pt C:432-60. doi: 10.1016/0076-6879(81)74031-x.
2
The stability of solubilized mammalian muscle acetylcholine receptors during purification by monoclonal immunoadsorption.
J Neurochem. 1984 Jan;42(1):59-64. doi: 10.1111/j.1471-4159.1984.tb09698.x.
3
Immunochemical tests of acetylcholine receptor subunit models.
Nature. 1984;311(5986):573-5. doi: 10.1038/311573a0.
4
Antigenic sites of the nicotinic acetylcholine receptor cannot be predicted from the hydrophilicity profile.
FEBS Lett. 1984 Mar 12;168(1):143-8. doi: 10.1016/0014-5793(84)80224-0.
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6
Antigenic sites of the nicotinic acetylcholine receptor.烟碱型乙酰胆碱受体的抗原位点。
Biochem J. 1985 Oct 1;231(1):245. doi: 10.1042/bj2310245a.
7
Synthesis of an antigenic site of native acetylcholine receptor peptide 159-169 of Torpedo acetylcholine receptor alpha-chain.电鳐乙酰胆碱受体α链天然乙酰胆碱受体肽159 - 169抗原位点的合成
Biochem J. 1985 Feb 15;226(1):193-7. doi: 10.1042/bj2260193.
8
Experimental autoimmune myasthenia gravis and myasthenia gravis: biochemical and immunochemical aspects.实验性自身免疫性重症肌无力与重症肌无力：生物化学和免疫化学方面
Ann N Y Acad Sci. 1976;274:254-74. doi: 10.1111/j.1749-6632.1976.tb47691.x.
9
Prediction and conformation by synthesis of two antigenic sites in human haemoglobin by extrapolation from the known antigenic structure of sperm-whale myoglobin.通过从抹香鲸肌红蛋白已知的抗原结构进行推断，对人血红蛋白中的两个抗原位点进行合成预测和验证。
Biochem J. 1977 Oct 1;167(1):275-8. doi: 10.1042/bj1670275.
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