Keratin 37/38 Polyclonal Antibody, 50ul Serum & Sample Tubes Mutations in PKD2 are associated

Mutations in PKD2 are associated with autosomal dominant polycystic kidney disease type 2

IFI16 encodes a member of the HIN-200 (hematopoietic interferon-inducible nuclear antigens with 200 amino acid repeats) family of cytokines

In other eukaryotes

MAD1L1 (MAD1 mitotic arrest deficient like 1) is a component of the mitotic spindle-assembly checkpoint that prevents the onset of anaphase until all chromosome are properly aligned at the metaphase plate

EBV infection membrane protein 1 (LMP1) is found to interact with this and other TRAF proteins

Keratin 37/38 Polyclonal Antibody, 50ul Serum & Sample Tubes Mutations in PKD2 are associatedThe protein encoded by KRT37 (keratin 37) is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12 q21 and have the same direction of transcription.