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Judul EVALUASI MENGENAI SPESIFISTTAS ANTIBODI MONOKLONAL K99 TERHADAP ANTIGEN PERLEKATAN ESCHERICHIA COLI ENTEROTOKSIGENIK / GOZALI R. MOEKTI
Pengarang GOZALI R. MOEKTI
SUPAR
KUSMIYATI
Penerbitan Balai Penelitian Veteriner, Bogor : Prosiding Seminar Teknologi Veteriner 7h., 1994
Deskripsi Fisik 12
Subjek ENGENAI SPESIFISTTAS ANTIBODI
Abstrak In attempt to develop an improved diagnostic tool for neonatal colibacillosis in calves, monoclonal antibodies (McAb) directed against K99-adhesin derived from a reference strain of enterotoxigenic Escheridda con (Compton, K12; K99) were produced. Specificity of McAb produced was evaluated using a slide conglutination teat, indirect enzyme-linked immunosothent assay (ELISA), and immunoblotting. Antigens used for the specificity testing were prepared from known E. coif K99 of bath homologous (Compton, KU; K99) and heterologous (841), field-isolates (BL413, G1231, G1150 and 2631), and those of known as 1(99-negative E. coil (i.e. types 1(88, F41 and 987P). The present study resulted in a panel of 20 hybridomas secreting antibodies specific to K99-adhesin. Two of the total hybridomas obtained, 11(99-B5 and 1K99-C9, were cloned consecutively producing 14 and 10 clones, which were then found to be stabile up to the second cloning. Of 24 McAbs produced from the total clones, three antibodies were tested usi
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No Barcode No. Panggil Akses Lokasi Ketersediaan
ARTVET0761 ARTVET0761 Dapat dipinjam Perpustakaan Balai Besar Pengujian Standar Instrumen Veteriner - Ruang Baca Umum Tersedia
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035 # # $a 0010-0924000064
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084 # # $a ARTVET0761
100 0 # $a GOZALI R. MOEKTI
245 1 # $a EVALUASI MENGENAI SPESIFISTTAS ANTIBODI MONOKLONAL K99 TERHADAP ANTIGEN PERLEKATAN ESCHERICHIA COLI ENTEROTOKSIGENIK /$c GOZALI R. MOEKTI
260 # # $a Balai Penelitian Veteriner, Bogor :$b Prosiding Seminar Teknologi Veteriner 7h.,$c 1994
300 # # $a 12
520 # # $a In attempt to develop an improved diagnostic tool for neonatal colibacillosis in calves, monoclonal antibodies (McAb) directed against K99-adhesin derived from a reference strain of enterotoxigenic Escheridda con (Compton, K12; K99) were produced. Specificity of McAb produced was evaluated using a slide conglutination teat, indirect enzyme-linked immunosothent assay (ELISA), and immunoblotting. Antigens used for the specificity testing were prepared from known E. coif K99 of bath homologous (Compton, KU; K99) and heterologous (841), field-isolates (BL413, G1231, G1150 and 2631), and those of known as 1(99-negative E. coil (i.e. types 1(88, F41 and 987P). The present study resulted in a panel of 20 hybridomas secreting antibodies specific to K99-adhesin. Two of the total hybridomas obtained, 11(99-B5 and 1K99-C9, were cloned consecutively producing 14 and 10 clones, which were then found to be stabile up to the second cloning. Of 24 McAbs produced from the total clones, three antibodies were tested using a slide agglutination test and proved to be reactive to K99 antigens prepared either from reference strains or field-isolates, but showed not to be reactive to 1(99-negative E. ca. Based on the indirect-ELISA, all McAbs produced so far were indicated to be only recognise 1(99 antigens. Moreover immunolgotting utukttaken in this study demonstrated that the 24 McAbs identify 1(99 antigen located at a molecular weight marker ranging from 16000 to 17,000 &ikons (D).
650 # 4 $a ENGENAI SPESIFISTTAS ANTIBODI
700 0 # $a KUSMIYATI
700 0 # $a SUPAR
990 # # $a ARTVET0761
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