Product description

This gene encodes a protein with structural similarities to complement component C9 that is important in immunity. This protein forms membrane pores that allow the release of granzymes and subsequent cytolysis of target cells. Whether pore formation occurs in the plasma membrane of target cells or in an endosomal membrane inside target cells is subject to debate. Mutations in this gene are associated with a variety of human disease including diabetes, multiple sclerosis, lymphomas, autoimmune lymphoproliferative syndrome (ALPS), aplastic anemia, and familial hemophagocytic lymphohistiocytosis type 2 (FHL2), a rare and lethal autosomal recessive disorder of early childhood. [provided by RefSeq, Aug 2017]

Specifications
Supplier
OriGene Technologies Inc
Shipping & storage
Shipping condition
Blue Ice
Storage temperature
-20°C

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PRF1 (GFP-tagged) - Human perforin 1 (pore forming protein) (PRF1), transcript variant 2

RG208940

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PRF1 (GFP-tagged) - Human perforin 1 (pore forming protein) (PRF1), transcript variant 2

RG208940

By filling out this form, you request a sample. You will receive an order confirmation within one working day. The order cannot be modified after receipt of the order confirmation.


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