產品與服務

Nomenclature: CB17/Icr-Prkdc^scid/IcrCr

Type: Inbred, immunodeficient

Origin: SCID mice possess a genetic autosomal recessive mutation Prkdc^scid. Discovered in 1980 by Bosma in C.B-17/Icr mice at Fox Chase Cancer Center. SCID mice show a severe combined immunodeficiency affecting both B and T lymphocytes. They have normal natural killer (NK) cells, macrophages and granulocytes. NCI received this mouse in 1991. To Charles River in 2014.

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