I wanted to make a 1x TBE solution from a 1 Litre bottle of Lonza Accugene 10x TBE buffer. However, instead of adding 9 Litres of milliq water to the buffer I added 10-11 litres of milliq water.
I wanted to know two things
[a] can i use this TBE as it is to make DNA gels for genotyping
[b] could i just get another bottle of 10x TBE add it to my existing stock then bring up to 20 litres with milliq to even out my error
OVERDILUTION OF TBE BUFFER
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