Sensitive enzyme immunoassay (immune complex transfer enzyme immunoassay) for (anti‐human T‐cell leukemia virus type I) IgG in serum using a synthetic peptide, Cys‐Env gp46(188‐224), as antigen
Sensitive enzyme immunoassay (immune complex transfer enzyme immunoassay) for (anti‐human T‐cell leukemia virus type I) IgG in serum using a synthetic peptide, Cys‐Env gp46(188‐224), as antigen
复制标题
使用合成肽 Cys-Env gp46(188-224) 作为抗原,对血清中的(抗人 T 细胞白血病病毒 I 型)IgG 进行灵敏酶免疫分析(免疫复合物转移酶免疫分析)
DOI:
10.1002/jcla.1860060206
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发表时间:
1992
影响因子:
2.7
通讯作者:
E. Ishikawa
中科院分区:
文献类型:
--
作者:
T. Kohno;I. Sakoda;E. Ishikawa
A sensitive enzyme immunoassay (immune complex transfer enzyme immunoassay) for (anti‐human T‐cell leukemia virus type I) IgG (anti‐HTLV‐I IgG) in serum using a synthetic peptide, Cys‐env gp46(188‐224) of HTLV‐I, is described. Anti‐HTLV‐I IgG in test serum, which had been incubated with excess of inactive β‐D‐galactosidase to eliminate interference by anti‐β‐D‐galactosidase antibodies, was reacted simultaneously with 2,4‐dinitrophenyl‐bovine serum albumin‐Cys‐env gp46 (188‐224) conjugate and Cys‐env gp46 (188‐224)‐β‐D‐galactosidase conjugate. The complex formed consisting of the three components was trapped onto polystyrene balls coated with affinity‐purified (anti‐2,4‐dinitrophenyl group) IgG. After washing to eliminate nonspecific IgG in the test serum and excess of the β‐D‐galactosidase conjugate, the complex was eluted from the polystyrene balls with ϵN‐2,4‐dinitrophenyl‐L‐lysine and transferred to polystyrene balls coated with affinity‐purified (anti‐human IgG‐γ‐chain) IgG. β‐D‐Galactosidase activity bound to the (anti‐human IgG‐γ‐chain) IgG‐coated polystyrene balls was assayed by fluorometry. This assay was more sensitive and useful than the immune complex transfer enzyme immunoassay using Cys‐Arg‐env gp46(188‐209) and other methods using HTLV‐I as antigen.
DOI:
--
发表时间:
1989
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Palker,TJ;Tanner,ME;Scearce,RM;Streilein,RD;Clark,ME;Haynes,BF
通讯作者:
Haynes,BF