Home page > Site Map
Site Map
Section : In the headlines
Articles and subsections :
Section : To be noted
Articles and subsections :
- 2016, May 19th, major Brucella database update
- 2018, Brucella version 4_3 database update
- Brucellosis 2008
- First MLVA ring trial : join now !
- Second MLVA ring trial : join now !
Section : News
Articles and subsections :
- 2016, May 16th, MicrobesGenotyping site released for beta-testing
- Brucella microti isolated from red fox in Austria
- Brucella microti isolated from soil
- Brucella2009 just released
- Brucella2010 released
- Brucella2012 released
- Diversity of clinical Brucella melitensis isolates in Lebanon
- MLST investigation within the Brucella genus
- MLVA analysis of Brucella isolates from human patients
- MLVA for Brucella by Le Flèche et al., 2006
- MLVA for Brucella by Whatmore et al., 2006
- MLVA ring trial 2007, current list of participants
- MLVA ring trial announcement : closing time
- MLVA typing of Brucella isolates from humans in Sicily, Italy
- New species Brucella microti validly published
- Stability of MLVA loci in the Brucella melitensis Rev1 vaccine strain
- The Brucella2007 MLVA database just released
- Two new species within the Brucella genus
Section : Curators
Articles and subsections :
Section : MLVA ring trials
Articles and subsections :
Section : MLVA Web service
Articles and subsections :
-
Brucella MLVA database
-
Frequently asked questions
- Do I need to do a PCR on the control strain each time a PCR for an "unknown" strain is setup? Or could I simply use leftover product from a previous PCR on the control strain to run on a gel with the products from the strains I am trying to type ?
- I can get the PCR assay to work, but am having problems analyzing the bands to get accurate sizes from my gels. I wonder how to actually calculate an exact band size and the repeat number. I am using the size markers to make a standard curve based on distance migrated on the gel. This old fashioned method is working, but once I get a band size, I cannot figure out how to get a repeat copy number.
- I do not have the 16M reference strain. Is it possible to use an other control strain ?
- Is it better to use agarose or capillary electrophoresis for MLVA typing?
- May I run different loci on the same agarose gel ?
-
Utilities (protocols, etc.)
Section : Related links
Articles and subsections :
