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Judul Recombinant LipL32 Protein for Leptospirosis Detection in Indonesia / Sumarningsih; Tarigan, Simson; Susanti; Kusmiyati (Balai Besar Penelitian Veteriner)
Pengarang Tarigan, Simson
Susanti
Kusmiyati (Balai Besar Penelitian Veteriner)
EDISI Procedia Chemistry
Penerbitan 2016
Deskripsi Fisik Vol.18. 2016
Abstrak Leptospirosis is an endemic zoonotic disease in tropical countries. However, detection using the microagglutination test (MAT) as a gold standard is difficult to perform in Indonesia. Therefore, recombinant LipL32 protein (rLipL32) has been studied as an antigen for an ELISA test to detect Leptospirosis. We produced rLipL32 using the pRSET-C vector and expressed it in E. coli BL21 (DE3) competent cells. Under native conditions, we purified 2 mg rLipL32 protein from 500 ml culture. Analysis using western blotting and ELISA showed that serum from the bovine positive MAT serovar Hardjo could recognize pure rLipL32 protein. This result confirms an earlier study that indicates that rLipL32 protein is a good antigen for Leptospirosis detection. The diagnostic assay using rLipL32 is safe because it does not use infectious bacteria as an antigen and because it is easy to perform in every diagnostic laboratory in Indonesia. However, further study
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No Barcode No. Panggil Akses Lokasi Ketersediaan
ARTVET2098 ARTVET2098 Dapat dipinjam Perpustakaan Balai Besar Pengujian Standar Instrumen Veteriner - Koleksi Agris Tersedia
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082 # # $a ARTVET2098
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245 # # $a Recombinant LipL32 Protein for Leptospirosis Detection in Indonesia /$c Sumarningsih; Tarigan, Simson; Susanti; Kusmiyati (Balai Besar Penelitian Veteriner)
250 # # $a Procedia Chemistry
260 # # ,$c 2016
300 # # $a Vol.18. 2016
520 # # $a Leptospirosis is an endemic zoonotic disease in tropical countries. However, detection using the microagglutination test (MAT) as a gold standard is difficult to perform in Indonesia. Therefore, recombinant LipL32 protein (rLipL32) has been studied as an antigen for an ELISA test to detect Leptospirosis. We produced rLipL32 using the pRSET-C vector and expressed it in E. coli BL21 (DE3) competent cells. Under native conditions, we purified 2 mg rLipL32 protein from 500 ml culture. Analysis using western blotting and ELISA showed that serum from the bovine positive MAT serovar Hardjo could recognize pure rLipL32 protein. This result confirms an earlier study that indicates that rLipL32 protein is a good antigen for Leptospirosis detection. The diagnostic assay using rLipL32 is safe because it does not use infectious bacteria as an antigen and because it is easy to perform in every diagnostic laboratory in Indonesia. However, further study is still required for field validation of the rLipL32 assay
700 # $a Kusmiyati (Balai Besar Penelitian Veteriner)
700 # $a Susanti
700 # $a Tarigan, Simson
990 # # $a ARTVET2098
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