B6;129-Tg(UBC-Dclre1c,-GFP)6Jpdv/Orl

Status

Available to order

EMMA IDEM:01806
Citation informationRRID:IMSR_EM:01806 

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International strain nameB6;129-Tg(UBC-Dclre1c,-GFP)6Jpdv/Orl
Alternative nameArtT
Strain typeTransgenic Strains
Allele/Transgene symbolTg(UBC-Dclre1c,-GFP)6Jpdv
Gene/Transgene symbolTg(UBC-Dclre1c,-GFP)6Jpdv

Information from provider

ProviderJean-Pierre De Villartay
Provider affiliationCRBS (Centre de Recherche en Biomédecine), Inserm UMR 1109 (Immuno-Rhumatologie Moléculaire, IRM)
Genetic informationThe transgene contains a floxed murine Artemis (DNA cross-link repair 1C, Dclre1c) coding sequence fused to a tandem affinity purification (TAP) tag sequence.
Phenotypic informationNot known.
Breeding historyBackcrossed to C57BL/6, F2.
References
  • A generic protein purification method for protein complex characterization and proteome exploration.;Rigaut G, Shevchenko A, Rutz B, Wilm M, Mann M, Séraphin B, ;1999;Nature biotechnology;17;1030-2; 10504710
  • Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.;Moshous D, Callebaut I, de Chasseval R, Corneo B, Cavazzana-Calvo M, Le Deist F, Tezcan I, Sanal O, Bertrand Y, Philippe N, Fischer A, de Villartay J P, ;2001;Cell;105;177-86; 11336668
  • Role for DNA repair factor XRCC4 in immunoglobulin class switch recombination.;Soulas-Sprauel Pauline, Le Guyader Gwenaël, Rivera-Munoz Paola, Abramowski Vincent, Olivier-Martin Christelle, Goujet-Zalc Cécile, Charneau Pierre, de Villartay Jean-Pierre, ;2007;The Journal of experimental medicine;204;1717-27; 17606631

Information from EMMA

Archiving centreCNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France

Literature references

  • A generic protein purification method for protein complex characterization and proteome exploration.;Rigaut G, Shevchenko A, Rutz B, Wilm M, Mann M, Séraphin B, ;1999;Nature biotechnology;17;1030-2; 10504710
  • Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.;Moshous D, Callebaut I, de Chasseval R, Corneo B, Cavazzana-Calvo M, Le Deist F, Tezcan I, Sanal O, Bertrand Y, Philippe N, Fischer A, de Villartay J P, ;2001;Cell;105;177-86; 11336668
  • Role for DNA repair factor XRCC4 in immunoglobulin class switch recombination.;Soulas-Sprauel Pauline, Le Guyader Gwenaël, Rivera-Munoz Paola, Abramowski Vincent, Olivier-Martin Christelle, Goujet-Zalc Cécile, Charneau Pierre, de Villartay Jean-Pierre, ;2007;The Journal of experimental medicine;204;1717-27; 17606631

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