Eric Schirmer Lab:
Schirmer lab plasmids
Unpublished
Unpublished
Plasmids from Article
| ID | Plasmid | Purpose |
|---|---|---|
| 61991 | NET43 pEGFP-N2 (609) | mammalian expression of nuclear envelope transmembrane protein |
| 61995 | NET92 pmRFP-N2 (643) | mammalian expression of nuclear envelope transmembrane protein |
| 62045 | NET29A.Mm pEGFP-N2 (1326) | mammalian expression of nuclear envelope transmembrane protein |
| 62046 | NET29b.Mm pEGFP-N2 (1327) | mammalian expression of nuclear envelope transmembrane protein |
| 62052 | NET29A.Hs pRRLSIN (1742) | lentiviral expression of nuclear envelope transmembrane protein |
| 62053 | NET29B.mm pRRLSIN (1744) | lentiviral expression of nuclear envelope transmembrane protein |
| 124262 | STING-V1 | C-terminally tagged STING with split Venus Construct for studying localisation of STING in different cellular compartments |
| 124263 | V1-STING | N-terminally tagged STING with split Venus Construct for studying localisation of STING in different cellular compartments |
| 124264 | STING-V2 | C-terminally tagged STING with split Venus Construct for studying localisation of STING in different cellular compartments |
| 124265 | V2-STING | N-terminally tagged STING with split Venus Construct for studying localisation of STING in different cellular compartments |
| 124266 | NLS-mRFP-V1 | Nuclear localised mRFP reporter construct with one half of split Venus |
| 124267 | NLS-mRFP-V2 | Nuclear localised mRFP reporter construct with one half of split Venus |
| 124268 | Lamin A-mRFP | Wild-type Lamin A, C-terminally tagged with mRFP |
| 124269 | Lamin A (R298C)-mRFP | Lamin A mutant (R298C), C-terminally tagged with Mrfp. Mutation associated with CMT neuropathy. |
| 124270 | Lamin A (R377H)-mRFP | Lamin A mutant (R377H), C-terminally tagged with mRFP. Mutation associated with EDMD myopathy. |
| 124271 | Lamin A (G465D)-mRFP | Lamin A mutant (G465D), C-terminally tagged with mRFP. Mutation associated with FPLD lipodystrophy. |
| 124272 | Lamin A (R527P)-mRFP | Lamin A mutant (R527P), C-terminally tagged with mRFP. Mutation associated with EDMD myopathy. |
| 124273 | Lamin A (R482Q)-mRFP | Lamin A mutant (R482Q), C-terminally tagged with mRFP. Mutation associated with FPLD lipodystrophy. |
| 124274 | Lamin A (R435C)-mRFP | Lamin A mutant (R435C), C-terminally tagged with mRFP. Mutation associated with Progeria. |