McClean: EDTA (0.5M): Difference between revisions

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==Overview==
==Overview==
Describe an overview of the procedure here.
EDTA is a synthetic amino acid and an agent that contains a typically organic ligand that bonds to a central metal atom. Enzymes that synthesize or modify nucleic acids (like polymerases, ligases, kinases, or nucleases) depend on Mg2+. With EDTA, it can stop the reactions between the enzymes and nucleic acids. EDTA is also in many buffers that store DNA (like TE buffer) removes the metal cofactors.  


==Materials==
==Materials==
# Item 1 with catalog number
# 186.1g disodium ethylenediamine tetraacetate •2H2 (Na2EDTA)
# Item 2 with catalog number
# 800mL of dH2O
# Item 3 with catalog number
# 50mL NaOH
 
# Aliquots


==Procedure==
==Procedure==
*Step 1
*Step 1 - Measure out 186.1g of Na2EDTA into a tall graduated cylinder 
*Step 2
*Step 2 - Add in 800mL of dH2O and stir vigorously on a magnetic stirrer with a stir bar
*Step 3
*Step 3 - Using glass electrode (?), identify the pH of the solution
*Step 4
*Step 4 - If the pH is not around 8.0, carefully add in NaOH to adjust the pH
*Step 5 - Bring the solution up to 1L and stir
*Step 6 - Dispense the solution into aliquots
*Step 7 - Sterilize by autoclaving


==Other Information==
==Other Information==
# If the pH of the solution is not adjusted to 8.0, EDTA will not dissolve.
# Store at room temperature
# For more chemical information, go to http://openwetware.org/wiki/EDTA


==Notes==
==Notes==
Line 20: Line 26:
#List troubleshooting tips here.   
#List troubleshooting tips here.   
#You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
#You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
#Anecdotal observations that might be of use to others can also be posted here.
#Anecdotal observations that might be of use to others can also be posted here.


Please sign your name to your note by adding <font face="courier"><nowiki>'''*~~~~''':</nowiki></font> to the beginning of your tip.
==References==
Promega Corporation. "Recipes for Common Laboratory Solutions" ''Promega: Technical Reference'' (2010) https://www.promega.com/~/media/files/resources/technical%20references/recipes%20for%20common%20lab%20solutions.pdf.


==References==
Department of Ecology and Evolutionary Biology-University of Michigan. "Recipe for Stock Solution" ''Genomic Diversity Laboratory'' http://www.lsa.umich.edu/gdl/forms/pdf/Recipes-Stock.pdf.


==Contact==
==Contact==

Latest revision as of 17:13, 29 April 2015

Overview

EDTA is a synthetic amino acid and an agent that contains a typically organic ligand that bonds to a central metal atom. Enzymes that synthesize or modify nucleic acids (like polymerases, ligases, kinases, or nucleases) depend on Mg2+. With EDTA, it can stop the reactions between the enzymes and nucleic acids. EDTA is also in many buffers that store DNA (like TE buffer) removes the metal cofactors.

Materials

  1. 186.1g disodium ethylenediamine tetraacetate •2H2 (Na2EDTA)
  2. 800mL of dH2O
  3. 50mL NaOH
  4. Aliquots

Procedure

  • Step 1 - Measure out 186.1g of Na2EDTA into a tall graduated cylinder
  • Step 2 - Add in 800mL of dH2O and stir vigorously on a magnetic stirrer with a stir bar
  • Step 3 - Using glass electrode (?), identify the pH of the solution
  • Step 4 - If the pH is not around 8.0, carefully add in NaOH to adjust the pH
  • Step 5 - Bring the solution up to 1L and stir
  • Step 6 - Dispense the solution into aliquots
  • Step 7 - Sterilize by autoclaving

Other Information

  1. If the pH of the solution is not adjusted to 8.0, EDTA will not dissolve.
  2. Store at room temperature
  3. For more chemical information, go to http://openwetware.org/wiki/EDTA

Notes

Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input!

  1. List troubleshooting tips here.
  2. You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
  3. Anecdotal observations that might be of use to others can also be posted here.

References

Promega Corporation. "Recipes for Common Laboratory Solutions" Promega: Technical Reference (2010) https://www.promega.com/~/media/files/resources/technical%20references/recipes%20for%20common%20lab%20solutions.pdf.

Department of Ecology and Evolutionary Biology-University of Michigan. "Recipe for Stock Solution" Genomic Diversity Laboratory http://www.lsa.umich.edu/gdl/forms/pdf/Recipes-Stock.pdf.

Contact

or instead, discuss this protocol.