Health Report

Nomenclature NOD.CB17-Prkdcscid/Arc
Product code NODSCID
Strain Description Mutant inbred
Coat Colour Albino (A/A Tyrc/Tyrc)
MHC Haplotype H2Kg7
Complement Factor C5 deficient
  • Prkdcscid – autosomal recessive, protein kinase, DNA activated, catalytic polypeptide.
  • No endogenous T- or B- lymphocyte function.
  • Develops high incidence of thymoma with age and old mice can develop inclusion body nephropathy.
  • Used for the delineation of the role of T cell subsets and auto-antibodies in diabetes.
  • Housed in an isolator.