should i be jealous...??

oh... i think i can't even have the choice to ask like that...
cause... i don't have the chance to choose i cannot to be jealous...
i just can't control what i feel...

wish she could be more sensitive just a little bit...
or should i just say to her directly??? but i'm no one to her...

i'm facing my exam tomorrow... i've try my best...

hah....
hi there....
i'm back....

wew... it seems that i really can't manage my own time...
poor me... i've always planned everything one night before of what i'm gonna do today... but always failed... =.="

well then.. just like today... i planned to study n i end up bloging, fb-ing, chatting n bla2....

n maybe tonight i'll out for soccer again.. waw.. haha

i hate they stop the sport class today.. damn
we suppose to play badminton... why should this happen to badminton...
it's my favourite sport... =.="

well then... since i've started my online-ing then i should continue... wahahaha....

then.. i'll just share my lab experiment yesterday...
it's quite cool ya know... haha
the first one is just kind of quick boring demonstration from my professor... so we didn't actually did sth... it called PCR (Polymerase Chain Reaction)

then the second one is cooler.. haha...
it's called agarose gel electrophoresis it's called Agarose, coz the gel is from the mixture from the agarose... haha... cool heh....
well then... i've got some picture of it...



it's the first tool to make the gel from the mixture of agarose n TAE (Tris-HCL Acetate EDTA) buffer... we then pour it into the medium that has black n white strip..




it's the apparatus to run the DNA through the gel... it worked by pulling the DNA mixture down through the gel... the apparatus worked with electromotive force...
by using the flow of the some kind of electricity from the negative charge(anode) to positive charge(cathode)...



well this is the gel... just like "agar agar" i really want to eat it... haha



and this is the gel that has been added the marker n the DNA solution... that has been rundown by the apparatus.. can be seen, the solution (blue) is most likely in the in the bottom.. this gel then will be put above the UV light so see the size of the DNA compare to the marker...




and this is the gel above the UV light... the size not really clear.. since it is blur... haha... poor you!!!

well then... it's really cool for me.. haha


bye2