Dear all,

I am working on a high glycosylated protein, which was produced from HEK293 
cells.  Last time I added glycosylation inhibitor, the protein could exist some 
monomers and dimers in a buffer pH5.4. This time I didn't add glycosylation 
inhibitor, the protein seems highly aggregated and couldn't be separated in the 
same buffer. Does anyone have any experience working with glycoprotein and 
could you give me some suggestions?  Many thanks in advance!


Best regards,


Yours sincerley,



Wei





[cid:image001.jpg@01CC116E.513B3050]


________________________________
Helmholtz-Zentrum f?r Infektionsforschung GmbH | Inhoffenstra?e 7 | 38124 
Braunschweig | www.helmholtz-hzi.de

Vorsitzende des Aufsichtsrates: MinDir'in B?rbel Brumme-Bothe, 
Bundesministerium f?r Bildung und Forschung
Stellvertreter: MinDirig Heiko Gevers, Nieders?chsisches Ministerium f?r 
Wissenschaft und Kultur
Gesch?ftsf?hrung: Prof. Dr. Dirk Heinz; Ulf Richter, MBA
Gesellschaft mit beschr?nkter Haftung (GmbH)
Sitz der Gesellschaft: Braunschweig
Handelsregister: Amtsgericht Braunschweig, HRB 477

<<inline: image001.jpg>>

<<attachment: Wei Li.vcf>>

Reply via email to