Laboratory Information
| Name | GZ View on WormBase |
|---|---|
| Allele designation | is |
| Head | Pierre Gonczy |
| Institution | Ecole Polytechnique Federale de Lausanne, Lausanne, Switzerland |
| Address | EPFL SV ISREC UPGON Station 19 Lausanne CH-1015 Switzerland |
| Website | http://gonczy-lab.epfl.ch |
| Gene classes | apo tac era |
Strains contributed by this laboratory
| Strain | Genotype | Species | Description |
|---|---|---|---|
| EU1004 | tac-1(or402) II. | C. elegans | Homozygous mutant animals give rise to >97% dead embyros at the restrictive temperature of 26C, with embryos exhibiting a lack of pronuclear migration at the one-cell stage. Homozygous mutant animals give rise to 50% dead embryos at the permissive temperature of 15C. Maintain at 15C. |
| EU1172 | zyg-9(or593) II. | C. elegans | Temperature sensitive. Maintain at 15C. At 26C, animals give rise to 99% dead embryos, with embryos exhibiting lack of pronuclear migration at the one-cell stage. At 15C, animals give rise to 73% dead embryos. |
| EU1355 | zyg-9(or628) II. | C. elegans | Temperature sensitive. Maintain at 15C. At 26C, animals give rise to 100% dead embryos, with embryos exhibiting lack of pronuclear migration at the one-cell stage. At 15C, animals give rise to 42% dead embryos. |
| EU1510 | zyg-9(or634) II. | C. elegans | Temperature sensitive. Maintain at 15C. At 26C, animals give rise to 100% dead embryos, with embryos exhibiting lack of pronuclear migration at the one-cell stage. At 15C, animals give rise to viable progeny. |
| EU944 | tac-1(or455) II. | C. elegans | Homozygous mutant animals give rise to >99% dead embyros at the restrictive temperature of 26C, with embryos exhibiting a lack of pronuclear migration at the one-cell stage. Homozygous mutant animals give rise to viable progeny at the permissive temperature of 15C. Maintain at 15C. |
| GZ264 | unc-119(ed3) III; isIs17. | C. elegans | isIs17 [pGZ295 (pie-1p::GFP::pcn-1(W03D2.4)) + pDP#MM051 (unc-119(+))] Maintain at 25C if possible to avoid possible germ line silencing. The entire coding sequence of PCNA (PCN-1, W03D2.4) was PCR-amplified and the resulting fragment cloned into pie-1::GFP germline expression vector to generate pGZ295, which was co-bombarded with pDP#MM051, which carries an unc-119 cDNA. The transgenic line behaves as though the two plasmids have been jointly integrated. |
| GZ491 | dpy-11(e224) sas-5(t2033) V/nT1 [let-?(m435)] (IV;V). | C. elegans |
This laboratory hasn't submitted any alleles to the CGC.