SC65 Polyclonal Antibody, 50ul Purification Mutations in THBD are a

Mutations in THBD are a cause of thromboembolic disease

that is exclusively expressed in adult skeletal muscle

CXCL3 encodes a member of the CXC subfamily of chemokines

Mutations in this gene cause autosomal recessive spastic paraplegia 7

SC65 Polyclonal Antibody, 50ul Purification Mutations in THBD are aThis nucleolar protein was first characterized because it was an autoantigen in cases on interstitial cystitis. The protein, with a predicted molecular weight of 50 kDa, appears to be localized in the particulate compartment of the interphase nucleolus, with a distribution distinct from that of nucleolar protein B23. During mitosis it is associated with chromosomes.