I'm isolating the nuclei of HepG2 cells using homogenization with the douncer, spinning at 1000 g obtaining crude nuclear fractions and then loading the CNF on sucrose gradient. BUT when i check with ER marker calnexin i find the nuclear fraction has even stronger bands than membrane fractions. That means that ER is not separated from nuclei. Any suggestions on how to obtain a nuclear fraction pure of ER?
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dan_
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Posted 22 June 2009 - 11:14 AM
Hi,
Qiagen has a kit that work well for this application : Qproteome cell compartment kit.
I presently use this kit I have always clean nuclear extract.
Hope this can help you.
Qiagen has a kit that work well for this application : Qproteome cell compartment kit.
I presently use this kit I have always clean nuclear extract.
Hope this can help you.
fred197237, on Jun 4 2009, 09:16 AM, said:
I'm isolating the nuclei of HepG2 cells using homogenization with the douncer, spinning at 1000 g obtaining crude nuclear fractions and then loading the CNF on sucrose gradient. BUT when i check with ER marker calnexin i find the nuclear fraction has even stronger bands than membrane fractions. That means that ER is not separated from nuclei. Any suggestions on how to obtain a nuclear fraction pure of ER?
