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Is agarose gel electrophoresis suitable for only gram negative plasmid DNA?

Agarose gel electrophoresis is suitable for ALL DNA.


What compounds form gel matrices suitable for electrophoresis?

its starch ,agarose and polyacrylamide by mkhaliphi dlamini


What are the application of paper electrophoresis?

Paper electrophoresis is used to analyze scientific experiments. One use in scientific experiments for paper electrophoresis is to determine the presence of HIV from blood samples.


Which technique was use to produce these bands?

Gel electrophoresis


Scientists use gel electrophoresis to cut dna at a specific nucleotide True or false?

It is true that Scientists use gel electrophoresis to cut DNA molecules at a specific sequence of nucleotides.


Is tgge and dgge same thing?

Temperature Gradient Gel Electrophoresis (TGGE) is a refinement of Denaturing Gradient Gel Electrophoresis (DGGE). Both use the same principles.


For what purpose might one use capillary electrophoresis?

Capillary electrophoresis is a technique used in laboratories to separate molecules based on their charge in order to study and analyze them. Capillary electrophoresis uses an electric charge to force the movement of molecules since each molecule will go a varying distance based on the weight of the molecule and their charge. Some areas of study that use capillary electrophoresis include DNA sequencing and pharmaceutical analysis.


What has the author A J Houtsmuller written?

A. J. Houtsmuller has written: 'Agarose-gel-electrophoresis of lipoproteins' -- subject(s): Blood protein electrophoresis, Electrophoresis, Gel electrophoresis, Lipoproteins


When was Electrophoresis - journal - created?

Electrophoresis - journal - was created in 1980.


What use is bacteria to copy DNA?

recombinant DNA technolog- apex


What is a common name for gel electrophoresis?

Agarose gel electrophoresis.


How do you avoid smearing of DNA bands in gel electrophoresis?

To avoid smearing of DNA bands in gel electrophoresis, ensure that the gel is properly prepared and poured to have an even surface. Use appropriate voltage and running conditions suitable for the size of DNA fragments being separated. Handle the gel carefully to prevent any unnecessary movement or disruption during loading and running.