"

From 2013.igem.org

Revision as of 18:16, 11 August 2013 (view source) E.Soboslay (Talk | contribs) ← Older edit		Revision as of 18:18, 11 August 2013 (view source) E.Soboslay (Talk | contribs) Newer edit →
Line 1:		Line 1:
	{{:Team:Glendale_CC_AZ/test}}		{{:Team:Glendale_CC_AZ/test}}
-	== NaCl Stress Growth Curve Assay ==	+
		+	== NaCl Stress Growth Assay ==
Line 10:		Line 11:
	-5 spec tubes		-5 spec tubes
-	-Spectrophotometer	+	-Spectrophotometer
	-Incubator at 37ºC		-Incubator at 37ºC
	-Micropipette		-Micropipette
Line 17:		Line 18:
	-NaCl		-NaCl
	- 250 mM IPTG		- 250 mM IPTG
		+
	== Procedure: ==		== Procedure: ==

---

Revision as of 18:18, 11 August 2013

NaCl Stress Growth Assay

Purpose: To measure bacterial growth with NaCl as DNA damaging agent

Materials:

-5 spec tubes -Spectrophotometer

       -Incubator at 37ºC

-Micropipette -Disposable micropipette tips -E. coli in LB media -NaCl - 250 mM IPTG

Procedure:

1. Grow E. coli in LB liquid media until stationary phase 2. To 4 separate spec tubes add: -1st: 5 mL of LB media -2nd: 5 mL of LB media supplemented with NaCl to a final concentration of 0.65 M NaCl -3rd: 5 mL of LB media supplemented with IPTG -4th: 5 mL of LB media supplemented with IPTG and NaCl to a final concentration of 0.65 M NaCl

3. Add 300 uL of bacterial liquid culture to each of the tubes. Use parafilm to seal them in order to minimize contamination. 4. Add 5.3 mL of LB media to the last spec tube which will be use to blank the spectrophotometer. Seal with parafilm. 6. Use Kimwipes to clean any prints or smear on the spec tubes. Invert each tube twice before placing in spectrophotometer. 7. Blank the spectrophotometer. Read absorbance of each spec tube. 8. Incubate all tubes at 37ºC for 3 hours. 9. Repeat steps 6-7 after 24 hours.