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Prep. of 50X TAE bufferModerator: BioTeam
8 posts • Page 1 of 1
Prep. of 50X TAE bufferHi everyone:
I am a new person to mol. bio. lab and I want to prepare 50 X TAE buffer. I did the follwoing: To make 1L of 50x TAE buffer: 242g Tris 100mL of 0.5M EDTA: This is prepared by (In 100 ml 1X PBS, Add 73.2 gram of EDTA) 57.1mL Glacial Acetic Acid Add enough MQ H2O to dissolve solids to final volume of 1000mL. Is my work right??? The pH of PBS is about 7.6, Is this Ok for TAE buffer or I have to get the pH to 8??? If i should increase the pH, how can I do this step?
Re: Prep. of 50X TAE bufferUnfortunately im not familiar with making TAE but i can give you some general advice. In this case you have to take in consideration not only the pH of the PBS solution but also the effect of the acetic acid (which will be "pulling" your pH down into acidic) so if yout pH is to low try lowering the pH by adding a base such as NaOH
EDTA is annoying to dissolve to say the least. It is slightly acidic, but disssolves only at pH 8. Also I usually do not prepare my solution in PBS but in water.
So take your PH meter, weigh your EDTA and add it to 80ml MQwater, then take a pipette, 10M NaOH and be patient. Patrick
Science has proof without any certainty. Creationists have certainty without any proof. (Ashley Montague)
No when you are preparing the 0,5M EDTA you first add 80ml of MQwater to the powder, and then try to dissolve the EDTA (it is a long and painful process, but it will eventually happen) by adding NaOH to the solution. And when all the powder has finally dissolved, you just complete to 100ml by adding MQwater again. Standard procedure to prepare a solution whose pH needs to be adjusted: leave space to add the solution that will adjust the pH.
Patrick
Science has proof without any certainty. Creationists have certainty without any proof. (Ashley Montague)
Re: Prep. of 50X TAE bufferMy impression is that there are two kinds of EDTA, one is very acid, another is close to 7. Correct if I am wrong. You need to use the right one for your buffer.
James Chou, Ph.D.
http://www.lifetein.com Understanding Life One Protein at a time... The Peptide Synthesis Service Company...
EDTA is a chemical. I guess it depends if you are discussing the protonated forms or the unprotonated forms. but for some reason, people don't seem to distinguish. i can't say really, i only use EDTA for DNA gel buffer, and that stuff is ready made.
"I have no intention of stopping anytime soon. I want to understand the universe and answer the big questions, that is what keeps me going" - Stephen Hawking
8 posts • Page 1 of 1
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