Production, purification and HRP conjugation of polyclonal IgG for ELISA test against rabbit Immunoglobulins in Wistar rats
Production, purification and HRP conjugation of polyclonal IgG for ELISA test against rabbit Immunoglobulins in Wistar rats
نویسندگان: مسعود مقدس زاده
کلمات کلیدی: Purification, Polyclonal antibody, Horse Radish Peroxides conjugation, Ion exchange chromatography.
نشریه: 0 , 1 , 18 , 2014
| نویسنده ثبت کننده مقاله |
مسعود مقدس زاده |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
مرکز تحقیقات بیوتکنولوژی(زیست فناوری) |
| کد مقاله |
71703 |
| عنوان فارسی مقاله |
Production, purification and HRP conjugation of polyclonal IgG for ELISA test against rabbit Immunoglobulins in Wistar rats |
| عنوان لاتین مقاله |
Production, purification and HRP conjugation of polyclonal IgG for ELISA test against rabbit Immunoglobulins in Wistar rats |
| ناشر |
6 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
خیر |
| عنوان نشریه (خارج از لیست فوق) |
Online Journal of Veterinary Research |
| نوع مقاله |
Original Article |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح چهار – Chemical Abstract - CAS |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
|
| Antibodies are used in many diagnostic and experimental procedures. The primary goal in experimental polyclonal antibody
production is to obtain sufficient volumes of high titer and high-affinity antibodies economically. Anti-rabbit Immunoglobulins and its conjugate with Horse Radish Peroxides (HRP) is used to diagnosis rabbit diseases by ELISA or western blotting tests. In this study, the production, purification and HRP conjugation of polyclonal IgG against rabbit Immunoglobulins in rats were carried out. Five 6-month-old Male Wister rats were immunized by rabbit Immunoglobulins in combination with Freund’s adjuvant. Purified antibody (using ion-exchange chromatography) was labeled to HRP. Direct enzyme linked Immune-sorbent assay (ELISA) was used to determine the optimum titer and cross reactivity of HRP conjugated IgG. The purity of various IgG preparations was about 98%. The optimum dilution of prepared HRP conjugated IgG was 1:25600. This conjugated IgG has no cross reactivity with guinea pig and hamster Immunoglobulins at optimized dilution. The result of the present study showed that ionexchange chromatography could be considered as an appropriate method for purification of
IgG antibodies. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| Moghadaszadeh2014.pdf | 1399/01/25 | 182950 | دانلود |