Welcome to the 2011 Symposium of the Danish Microbiological Society (Download as pdf)
We welcome you to a day with collaegues in microbiology, the invited speakers, many posters and technical exhibitions from companies that provide products for microbiological research.
The programme gives ample time for networking, poster viewing and visiting booths for companies sponsoring the meeting. LOOKING FORWARD TO SEEING YOU
Registration for 2011 Symposium of DMS:
Click here to go to the registration form
Or send an e.mail to
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and provide your
Name:
Institution/Company:
Department:
Address:
Postal code, city:
EAN number (Danish public institutions only):
Email
If you are bringing a poster, please attach abstract to mail as a MS Word 2003 document:
We will send an invoice to your institution/company. However if your institution/company is not paying the symposium for you, you must pay 600 kr. to: Danske Bank reg. no. 1551. Account no. 4590536865. Give your name and email in the payment.
Your abstract should be attached the email as a MS Word 2003 document using Arial 11 and in the format of the following example:
THE USE OF Q-PCR TECHNIQUES TO QUANTIFY NUMBERS OF Xxxxx sp. IN BLOD SAMPLES
Hans Hansen1, Mette Jensen2 & Anita Morales1
1: Technical University of Denmark, 2: University of Copenhagen
Quantitative real-time PCR was used to assay spirochetes in feeding ticks. Spirochetes in tick midguts increased sixfold, from 998 per tick before attachment to 5,884 at 48 h of attachment. Spirochetes in tick salivary glands increased >17-fold, from 1.2 per salivary gland pair before feeding to 20.8 at 72 h postattachment. The period of the most rapid increase in the number of spirochetes in the salivary glands occurred from 48 to 60 h postattachment; this time period coincides with the maximal increase in transmission risk during nymphal tick feeding An in vitro model of supragingival plaque associated with gingivitis was characterized by traditional culture techniques, comparative 16S rRNA gene sequencing of isolates, and quantitative PCR (QPCR). Actinomyces naeslundii, Prevotella spp., and Porphyromonas gingivalis increased under conditions emulating gingivitis. Gram-negative species and total bacteria were dramatically underestimated by culture compared to the estimates obtained by QPCR. (Abstract:Max 200 ord) |
Application for student stipend
Please send your registration information together with your abstract to
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. Please note in the subject line ”student stipend application”. Those selected for a student stipend will be notified directly.
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