T Stockholm Kirby Bauer Protocol

  • Uploaded by: Handayan Htb
  • 0
  • 0
  • August 2019
  • PDF

This document was uploaded by user and they confirmed that they have the permission to share it. If you are author or own the copyright of this book, please report to us by using this DMCA report form. Report DMCA


Overview

Download & View T Stockholm Kirby Bauer Protocol as PDF for free.

More details

  • Words: 343
  • Pages: 1
Lab Protocol

Updated: October 4th, 2016

iGEM Stockholm 2016

Kirby-Bauer Disk Diffusion Test Aim Preparing plates with bacterial inoculum and adding filter papers soaked in samples to assess whether the samples have a bactericidal or bacteriostatic function.

Procedure 1. Prepare sterile Whatman filter paper with a hole punch and also antibiotic free agar plates. For better visualisation MacConkey or Endo Agar can be used. Up to 6 samples or controls can be tested on one plate. 2. Streak 50 µl of a bacterial culture with approximately OD600 0.6 onto the plates. After streaking in one direction, rotate the plate by 90◦ and repeat the spreading (without applying more liquid culture) until the plate has completed a full turn. This step is essential to assure even distribution of the bacteria! 3. Do not turn the plates upside down as usual, instead let dry at RT while preparing samples. 4. When preparing samples, make sure to include proper positive and negative controls. For cell lysates, a good negative control is lysate from untransformed cells as well as sterile water. Kanamycin at 35 ug/ml (1:1000 dilution from stock) serves as a positive control. 5. Use tweezers to place filter papers onto an empty petri dish and pipet 20 µl of sample / control onto each paper. Let soak for a bit before ’dragging’ the papers out of the liquid and dabbing them onto an empty part of the dish to remove excess liquid. 6. Place filter papers onto agar, making sure to use proper sterile technique. 7. Let the plates dry as in step (3) or place them in the incubator lid facing up if drying at RT takes too long. 8. Check your plates after 12 h (ideally) and 24 h for bacterial growth and to check for halos. Take pictures of the halos and measure their radius.

Note! It is very important to work with sterile equipment and reagents in this case to assure that no contaminants influence bacterial growth.

Sources http://www.globe-network.org/sites/default/files/sites/default/files/documents/disk-diffusion-susceptibilitiesen_0.pdf retrieved 25.09.2016) http://www.antimicrobialresistance.dk/data/images/protocols/sop_dd_2010gfnlab002_v2.pdf retrieved 25.09.2016) https://www.addl.purdue.edu/newsletters/1997/spring/dds.shtml retrieved 25.09.2016)

Page 1 of 1

Related Documents

Stockholm Marathon
May 2020 5
Scott Bauer
June 2020 6
Wolfgang Bauer
December 2019 20
Stockholm City_draft2a
November 2019 11

More Documents from ""

Eye1994125.pdf
August 2019 18
Disfungsi
August 2019 19
Pediatric_book_rev2.pdf
August 2019 11
No.docx
August 2019 18