Tctex5 Polyclonal Antibody, 100ul Tubes DefectsF8 results in hemophilia A

DefectsF8 results in hemophilia A

Recessive mutations in this gene have been associated with a hereditary form of spastic paraparesis (HSP)

The binding of this protein to double-strand DNA induces a DNA topological change

With a capacity of 100-1000μl

The enzyme has strong sequence homology with prolylcarboxypeptidase and is active at both acidic and neutral pH

Tctex5 Polyclonal Antibody, 100ul Tubes DefectsF8 results in hemophilia APPP1R11 (protein phosphatase 1 regulatory inhibitor subunit 11) encodes a specific inhibitor of protein phosphatase 1 (PP1) with a differential sensitivity toward the metal independent and metal dependent forms of PP1. PPP1R11 is located within the major histocompatibility complex class I region on chromosome 6.