Judul | Recombinant LipL32 Protein for Leptospirosis Detection in Indonesia / Sumarningsih |
Pengarang | Sumarningsih Simson Tarigan Susanti Kusmiyati |
Penerbitan | 2015 |
Deskripsi Fisik | 8art |
Subjek | Recombinant LipL32 |
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 is still required for field validation of the rLipL32 assa |
Bentuk Karya | Tidak ada kode yang sesuai |
Target Pembaca | Tidak ada kode yang sesuai |
No Barcode | No. Panggil | Akses | Lokasi | Ketersediaan |
---|---|---|---|---|
00000033195 | Dapat dipinjam | Perpustakaan Balai Besar Pengujian Standar Instrumen Veteriner - Ruang Baca Umum | Tersedia |
Tag | Ind1 | Ind2 | Isi |
001 | INLIS000000000019178 | ||
005 | 20240911113339 | ||
007 | ta | ||
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245 | 1 | # | $a Recombinant LipL32 Protein for Leptospirosis Detection in Indonesia /$c Sumarningsih |
260 | # | # | ,$c 2015 |
300 | # | # | $a 8art |
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. |
650 | # | 4 | $a Recombinant LipL32 |
700 | 0 | # | $a Kusmiyati |
700 | 0 | # | $a Simson Tarigan |
700 | 0 | # | $a Susanti |
No | Nama File | Nama File Format Flash | Format File | Action |
1 | 2186.pdf | ARTVERT2186 | Baca Online |
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