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Questions related from Philippe Leone
I have a lot of RNAse-free filter tips with an expiration date that has run out since a more or less long time (2017 and even 2014!). Do you think I could I use them anyway without much risk to...
12 December 2018 7,318 0 View
I have an antibody recognizing my protein in its unfolded state, so I can visualize it by western-blot after SDS-PAGE. Unfortunatly, I can't see it after native-PAGE to follow its...
09 September 2014 553 7 View
I generated stable HEK lines, but some lines tend to clump (others not), and when I try to separate the cells by pipetting, lots of them dye. As I intend to run flow cytometry, I guess cell...
04 April 2013 8,033 5 View
I want to use HEK cell for stable selection, I know 293T are not suitable, and I found a batch of 293F (supposed to be cultured in suspension but that seem to grow very well as adherent cells...)....
02 February 2013 4,944 2 View
My plasmid contains a SV40 origin and a Neo selection marker; if I select 293T cells I have to use another antibiotic (and make a co-transfection with a second plasmid for the selection), if I use...
01 January 2013 2,090 1 View
They are not immortalised, contrary to 293T cells.
01 January 2013 5,662 2 View
I want to select stable HEK with Geneticin in order to express a membrane receptor and run functional studies (overexpression is not important). I read that HEK293Ts are not the best cells for...
01 January 2013 2,831 12 View