Simonsen H B
Acta Vet Scand. 1972;13(2):266-8. doi: 10.1186/BF03548582.
Immunological species differentiation of keratein from hair has previously been demonstrated by the precipitin ring test in tubes ( 1939) and by the indirect hemagglutination test ( 1970). In the present study the possibility of species identification of s-carboxymethylkeratein (SGMK) from single hairs was examined. SCMK and rabbit anti-SCMK sera from man, horse, dog and ox were prepared according to methods described by (1962) and (1970, 1971). Suitable antisera were used for the indirect hemagglutination-inhibition (IHI) test ( 1954). The antisera were absorbed with heterologous SCMK and the inhibition test performed using SCMK extracted from 5 cm stretches of hairs by reduction and alkylation in 1 ml fluid volumes. To each vial containing 0.5 ml of antiserum in a serial 2-fold dilution row of the respective antisera was added 0.05 ml of a homologous or a heterologous single-hair SCMK. After incubation at 37 °C for 30 min. SCMK-coated goat erythrocytes were added and the test read after incubation at 20 °C for 18 hrs.
角蛋白与毛发的免疫物种鉴别先前已通过试管沉淀环试验(1939年)和间接血凝试验(1970年)得到证实。在本研究中,对从单根毛发中鉴别s-羧甲基角蛋白(SGMK)的物种可能性进行了检测。根据(1962年)以及(1970年、1971年)所述方法制备了人、马、狗和牛的SCMK以及兔抗SCMK血清。使用合适的抗血清进行间接血凝抑制(IHI)试验(1954年)。用异源SCMK吸收抗血清,并使用通过在1毫升液体体积中还原和烷基化从5厘米长的毛发中提取的SCMK进行抑制试验。在各自抗血清的系列2倍稀释排中,向每个含有0.5毫升抗血清的小瓶中加入0.05毫升同源或异源单根毛发SCMK。在37℃孵育30分钟后,加入包被有SCMK的山羊红细胞,并在20℃孵育18小时后读取试验结果。