𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Rapid, sensitive detection ofBrucella abortusby polymerase chain reaction without extraction of DNA

✍ Scribed by A. Fekete; J. A. Bantle; S. M. Halling; M. R. Sanborn


Book ID
104647188
Publisher
Springer-Verlag
Year
1990
Tongue
English
Weight
564 KB
Volume
4
Category
Article
ISSN
0951-208X

No coin nor oath required. For personal study only.

✦ Synopsis


A freeze-thaw method was used to release DNA from acetone-killed, dried Brucella abortus S19 cells for polymerase chain reaction. A 635 bp fragment of a 43 kd membrane protein gene was amplified and detected by agarose gel electrophoresis. The sensitivity of the detection was as little as 100 fg of cells/sample.


πŸ“œ SIMILAR VOLUMES


Rapid and sensitive detection of Mollicu
✍ Mohammad Hassan Shahhosseiny; Zahra Hosseiny; Hamid Reza Khoramkhorshid; Shahram πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 289 KB πŸ‘ 1 views

## Abstract Infections with __Mollicutes__ species (such as __Mycoplasma__, __Acholeplasma__, and __Ureaplasma__) can induce a variety of problems in living organisms and laboratory cell cultures. Therefore, it is necessary to establish a routine diagnostic protocol for __Mycoplasma__ infection in

Sensitive and rapid detection of norovir
✍ Setsuko Ishida; Shima Yoshizumi; Tetsuya Ikeda; Masahiro Miyoshi; Motohiko Okano πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 296 KB πŸ‘ 1 views

## Abstract Conventional reverse transcription‐polymerase chain reaction (RT‐PCR) to detect norovirus (NV) is a complex of multi‐step procedure that requires gel electrophoresis as well as hybridization or sequencing to confirm the final diagnosis. A duplex TaqMan RT‐PCR was developed to detect and