Hi, There are different opinions about this but primarily it depends on the cells that you are growing. In differentiated cell lines the cells wont get reclocked at all. In the lab I work in, we dont consider that the cells can be reclocked. The best way of labelling would be labeling the cell lines...

2. Different cancer cells will definitely require different media. But the general procedure assuming you need to get cells from a particular tissue would be to get the tissue, extract the cells, digest ECM..., try culturing them in a flask / Tissue culture plate (depending on the type of cells it c...

Its been so long since I have won this game, didnt get anything specific by winning but then if its the moment that counts, then I win.
I know this win wont last too long.

Note to self - once a winner always a winner!

knowing the organism is crucial but given that its a general question a general answer would be that you would use a nucleotide blast (given that you have the gene sequence).

Seemed so to me too. Thank you so much

I am not very sure now it seems so. But yes a clarification would help.
Thanks though.

I do not understand what is meant by splice isoforms. I used to think that they are the products of alternate splicing. But I was reading a paper on: "mTORbeta Splicing Isoform Promotes Cell Proliferation and Tumorigenesis" And I got confused and decided to get the basic definition right. ...

Ahh back I am.

For Q2 D is right for in meiosis 1 there is a separation of homologous chromosomes and not chromatids.

I wiiiinnnn

If you must have noticed the proteins travel from one organelle to another. This transport is made possible by the vesicles. Now one can ask why does this have to be so? Its simple a protein needs to reach a specific place for its post translational modification and there must be something that must...

I am the next one i presume lol