Ask Your question
Need a fast expert's response?Submit order
and get a quick answer at the best price
for any assignment or question with DETAILED EXPLANATIONS!
Search & Filtering
glucose, 5 grams (g); NH4Cl, 1g; KH2PO4, 1g; MgSO4, 0.3g; yeast extract, 5g;
distilled water, 1 litre
(1) Gel filtration chromatography
(2) Paper chromatography
(3) Affinity chromatography
(4) Thin layer chromatography
My attempt at a solution:
Well, the analyte contains salt (possible inorganic so the particles, ions will be small enough as compared to a protein) and protein (a large one) so SEC or gel filtration looks perfect.
But there's affinity chromatography too. Two things come to my mind: 1.having an antibody or enzyme in the stationary phase will definitely work at holding back the proteins 2. but there may be some non specific polar interactions between the protein and the ions, so... (1) 's the right one?
a. Cation exchange b. Anion exchange c. gel filtration d. Reverse phase
Since the net charge is the same so there's no point using ion-exchange.
Gel filtration or Size exclusion rules out as the sizes are the same.
So the only thing left to be exploited is the hydrophobicity of the side-chain of amino acids.
I have a feeling that hydrophobic interactions are least in proteins, less no. of hydrophobic groups are to be found in one as compared to polar groups. So using reverse will be best because...
Well I think I'm missing out something. Aren't we suppose to decide the combination of stationary and mobile phases based on the component of analyte we want to elude at the end?
1) alcoholic fermentation 2)lactic fermentation 3) glycolysis 4)kreb cycle
I have to ask you one qustions that I dont quite understand. What is the number of alleles at each locus approximately and how many are there in the human genome? Does it have to do something with chromosome nuber?
Thank you in advance