- Messages
- 9
- Reaction score
- 14
- Points
- 13
thanks A TON!!!
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My pleasurethanks A TON!!!
First we should discuss this one ? :SAnd question 2.
Tell me anything u remember, specially abt percentage decrease and question abt standard error.First we should discuss this one ? :S
Infact I'm bit confused about Q2 Don't remember :'D
I think My percentage decrease was in 80's :S If I am not wrong :/Tell me anything u remember, specially abt percentage decrease and question abt standard error.
what was your % decrease of enzyme activity for y?What does the standard error show u abt the reliability of the data?
same value was calculated by me (Y) it was 83.33 but as the question was to the nearest whole number so 83 was the answer Hyna?
I dont think it is correct, because different size of fragments move the same distance in all the electrograms regardless of the Res Enzyme used. Only the distance move by different sizes of fragments changes when P.D is variable or AGAROSE is changed. but the investigation was to check the effect of different REs EnzymesFor C (i) i wrote the distances moved by different sizes of fragments. will it be considered correct? :3
Actually 24 hrs have passed :'DAs far as I know you should not discuss the paper before 24 hour it has been over so you might be in trouble
god bless !
I wrote from right to left and complimentaryWhat about the nucleotide sequence? Which way did you have to read it? I wrote it from left to right.
I wrote exactly the same constantsFor The controlled variables i wrote: 1) keep the concentration of the restriction enzyme constant in all samples. 2) Keep the tempfor restriction enzymes sample constant.
For the One relating that how we can say Eco R1 and Hin D3 have some fragments within themselves (dont know the exact wording though) i wrote some of the fragments from both show same movement..
For the part relating why student hypothesis is not correct.. i wrote the no. of sample is less no repeats so data may be anomalous..
Are they correct??
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