Video used for teaching on module 400484 Cells and Organelles at the University of Hull
Пікірлер: 34
@user-gp1xh7sq6h2 жыл бұрын
Your videos save my entire university career!! Thank you for all you do,
@katharinehubbard50432 жыл бұрын
Happy to help!
@haimschan Жыл бұрын
Wow! I can't really express in words how grateful to you. You save me. Thank you.
@danieloulhint7914 Жыл бұрын
This is the best video about Spectrophometer ever. I really learned alot. Thank you so much for the time you took to make it so simple. Kudos. Daniel from USA
@marielyrodriguesmarson2232 жыл бұрын
Congratulations!!!! I really appreciated your video!
@BeKaTcHosShow4 ай бұрын
Thank god I found this video! Saved my life🥹
@patrickedgmon79884 ай бұрын
I did some research and found that the incident light is not white light. It’s a certain color of light frequency split by a prism that is directed through the sample in a spectrophotometer. Then you can also measure each of the other light frequencies from the prism by directing them through the sample. This is what gives a unique set of readings that identifies the substance. This is why spectrophotometer are more expensive than colorimeter which uses a set of R,G,B filters. Wouldn’t this mean that Tommy’s device is really a colorimeter and not a spectrophotometer as he states in his subject title?
@Jun-dl5ni Жыл бұрын
Big thankful of your video. I watched your video for my knowlodge. and this is the best video of spectrophotometers. but I think my brain diden't want to know all of this things lol..
@5minshandcraft1234 ай бұрын
Thank you so much Love from pakistan. Literally you helped me.
@JuliaKaratoАй бұрын
How is no one talking about her perfect arrows??? Great video btw
@plutoniumiscool2 жыл бұрын
What is the extinction coefficient for amaranth red dye that has a max absorbance at 520nm?
@RemyVincent-yv6bd4 ай бұрын
Thank you.
@perputualwritersblock7 ай бұрын
this was really a fantastic video! quick question, for a lab I'm doing i need to measure coppersulphate concentrate at the beginning and end of my experiment. could i then use a calibration curve? also, what method/adaptions should i do if i add nitrogen fertlizer into the solution but only want to measure copper?
@eloisepearce79497 күн бұрын
Thank you so much! Please could I ask how you would estimate an Amax value based on the experimental data?
@ghayahyousef1649 Жыл бұрын
thank you !!
@LarsMartinGihle9 ай бұрын
great video. Would take 5 hour long lectures at school...
@abhijit21009 ай бұрын
Can you give a reference for the material you are covering? It will be really helpful for me to learn.
@ahmadelkassem33322 жыл бұрын
Thank you for this great video I want to ask about the concentration you calculate at the end is that we put in on the curve graph
@katharinehubbard50432 жыл бұрын
Hi there - glad you enjoyed the video. No - the two things are separate methods. Beers law describes a linear relationship between absorbance and concentration for molecules that absorb light *directly* - if you plotted the graph it would be a straight line. This works for molecules like chlorophyll and NADH which absorb light directly and are relatively unaffected by temperature/pH etc, hence you can mathematically predict the concentration with Beers law for these molecules. The calibration curve method is used for measuring molecules that *indirectly* absorb light eg via a chemical reaction. The classic example for the curve method would be using Bradfords reagent to measure protein concentration - the reaction between Bradfords and the protein causes the Bradfords reagent to change colour which you can measure on the spectrophotometer. This is a non-linear relationship that will depend on the temperature/pH/buffer, which is why you need to construct the calibration curve every time you want to make measurements. Hope that helps!
@ahmadelkassem33322 жыл бұрын
@@katharinehubbard5043 Thank you for answering I got it ❤❤❤
@abdullahidigale6698 Жыл бұрын
Tnk u very much
@TrucNguyen-ew3tw Жыл бұрын
I wonder how we know that our samples are indirectly resulted in abs or not. For example, does H2O2 create a linear or curved standard curve?
@katharinehubbard5043 Жыл бұрын
If your molecule absorbs light directly it will be a linear curve, if you measuring indirectly via an assay it will probably be curved. H2O2 absorbs directly in the UV range at 240, or you can measure indirectly via xylenol orange assay, which would need a standard curve making. Hope that helps!
@dr.satyabratasahoo564423 күн бұрын
Nice
@SHDEdits8 ай бұрын
A bit confusing to use percentage to illustrate I0 and I, as it’d be an absolute quantity of irradiance rather than a fraction to anything. Would make more sense to illustrate the initial fraction via transmittance, then show absorbance as the anti logarithm to the base 10 of that.
@saharmuhamed60793 ай бұрын
Can i know the matters which can be measured by it and the matters can't
@linusfrancis69064 ай бұрын
Is epsilon the same as wavelength?
@katharinehubbard50434 ай бұрын
No - wavelength uses the lambda symbol. Epsilon is a measure of how inherently absorbent a particular molecule is at a particular wavelength, so acts as a calibration constant
@linusfrancis69064 ай бұрын
My assignment has asked me to calculate the concentration of several solutions using beer's law - we calculated their absorbance and I'm assuming L is 1cm - so by converting the equation C = A/EL - but it hasn't given us an epsilom symbol, @@katharinehubbard5043
@nahlaessam26882 жыл бұрын
how could it be NONLINEAR? IT IS LINEAR
@katharinehubbard50432 жыл бұрын
I should have probably done this explanation the other way around. For molecules that absorb light directly (eg NADH, chlorophyll, DNA) the relationship will definitely be linear. However for some spectrophotometer assays that measure concentration indirectly there will be saturation. The obvious example here is a Bradford assay to measure protein - the Bradford reagent is only sensitive to low/medium protein concentrations, and saturates at high concentration. The relationship between protein concentration and absorbance is therefore non linear, so the standard curve method is used. Hope that makes things clearer!
@migueljuanbartolo2654 Жыл бұрын
@@katharinehubbard5043so if you're measuring protein by a dye-binding method, could the relationship be linear if solutions are very dilute?
@teebaya Жыл бұрын
الصووت حلوو
@AmruMagdy9 ай бұрын
Your videos save my entire university career!! Thank you for all you do,