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What would happen if a TLC plate was placed in a jar where the solvent level was above the level of the origin sample spot)? What should you do if you inadvertently...

Question

What would happen if a TLC plate was placed in a jar where the solvent level was above the level of the origin sample spot)? What should you do if you inadvertently spotted your plate too low (aside from consulting your TA)?

What would happen if a TLC plate was placed in a jar where the solvent level was above the level of the origin sample spot)? What should you do if you inadvertently spotted your plate too low (aside from consulting your TA)?



Answers

What would happen during an amino acid sequencing experiment using the Edman degradation if you accidentally added twice as much Edman reagent (on a per-mole basis) as the peptide you were sequencing?

Suppose we are having a parallel plate capacitor given to us with the passage ins is given as a silent idea. No, You mean sir, A dry electric slab in splits was dialectic constant. It's OK than the capacitance we become. Hey, times means the capacitance may increase like it times, but in place off dialect rid if we insert a metallic slept between the place Do you do this metal? The slaves off the passenger will get sure who's a short circuit will happen here in this circuit so we can see the capacity gens off. The capacity will become in finite, infinite capacitance means now the charge will not get a story in it. The charge will just pass through. It simply passed. It means it's the passages is now in a finite. It can store in finance of us. It can be stored in final charge for it. Or you can also see the bastard has mean damaged. Thank you

Hello everyone. So we know that proteins are released soluble in their eyes electric points. And this question is asking what will happen if we added small drops of its cl. So to start with we know that the Aizu electric point is is where the protein will have no net electric charge, meaning it's neutral at the state. And usually, as we said, it's the least soluble if we added SCL, meaning that the solution will be acidic and if it's acidic, the groups will be protein ated, meaning the structure will be as follows, the car broke silk milk and this is the mini grill and the side chain, whatever the side chain is. So if it's in the acidic uh solution it will acquire a total of positive charge on this structure and hence it will be more soluble and water. Okay?

So if DNA were to be coded for a protein and contain the wrong bay sequence, Um, uh, cells may mutate and improperly function.

Hello. So today we're answering question number 26. Predict what? What might happen if the DNA that code for a protein contained the wrong based sequins? So, taking a look at the chart I have up going across the first row, we have our normal based sequence, Our control. Okay, So for each of these amino acid based sequences off three a u g g c, c, t g, c et et cetera Oh, each of these code for a specific protein. So, for example, my thiamine Alan E insisting life seen et cetera. So there's a couple different things that can happen if each of those amino acids are either switched out for something else or they don't exist. So going across the second row, Ah, silent mutation is when we switch out one of our amino acids and it doesn't actually result in a different protein sequence. So in this case, yes, we switched out. The timing for the site is een, but our end result is still in Alan and protein. That's a silent mutation. A nonsense mutation is when the new base sequence results in the ending of coding protein altogether. So now, instead of instead of creating any protein, there's no protein being made, and then a miss sense mutation is when a change in the base sequence causes a different protein to be made altogether.


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