Spira G, Biswal N, Dreesman G R
Appl Microbiol. 1974 Aug;28(2):239-44. doi: 10.1128/am.28.2.239-244.1974.
Iodination of disrupted Moloney strain murine sarcoma-leukemia virus resulted in labeled group-specific (gs) protein which was subsequently purified on an isoelectrofocusing column. This iodinated purified gs antigen, prepared from a relatively small quantity of purified virus, was used in a radioimmunoassay. A radioimmunoassay inhibition method was developed so that antibody specific for mammalian C-type gs antigen could be measured in undiluted or low dilutions of test serum without altering the known reagents of the test. The gs antigen isolated from purified Moloney strain murine sarcoma-leukemia virus has an isoelectric point (pH 5.95) which is significantly lower than that reported for other murine leukemia viruses.
对破坏后的莫洛尼氏鼠肉瘤 - 白血病病毒进行碘化处理,产生了标记的群特异性(gs)蛋白,随后该蛋白在等电聚焦柱上进行了纯化。这种由相对少量纯化病毒制备的碘化纯化gs抗原被用于放射免疫测定。开发了一种放射免疫测定抑制方法,这样就可以在未稀释或低稀释度的测试血清中测量针对哺乳动物C型gs抗原的抗体,而无需改变测试的已知试剂。从纯化的莫洛尼氏鼠肉瘤 - 白血病病毒中分离出的gs抗原的等电点(pH 5.95)明显低于其他鼠白血病病毒报道的等电点。