Type i interferonopathy due to a homozygous loss-of-inhibitory function mutation in stat2

HIGHLIGHTS

SUMMARY

    Duncan et_al subsequently described two patients from the same family with a homozygous STAT2 mutation specifically affecting this negative_feedback regulatory role of STAT2. Shortly thereafter, Gruber et_al identified another patient with a mutation involving the same amino_acid residue of STAT2. Lentiviruses were produced by co-transfection of pCMVVSV-G (Addgene plasmid no. 8454), psPAX2 (Addgene plasmid no. 12260), and lentiviral transfer plasmid (pHRSIN-CSGW-STAT2 WT, pHR-SIN-CSGW-STAT2 p.(A219V), or pHR-SIN-CSGW-STAT2 p.(R148W)) in HEK 293FT_cells using Lipofectamine 2000 Transfection Reagent (11,668,019, Invitrogen,). The p.(A219V . . .

     

    Logo ScioWire Beta black

    If you want to have access to all the content you need to log in!

    Thanks :)

    If you don't have an account, you can create one here.

     

Scroll to Top

Add A Knowledge Base Question !

+ = Verify Human or Spambot ?