p56Dok-2(Phospho-Tyr351) Rabbit Polyclonal Antibody, 100ul Sampling Tubes Mutations in this gene result

Mutations in this gene result in Bernard-Soulier syndromes and platelet-type von Willebrand disease

a chromosomal region involved in both translocations and deletions in human malignancies

PSCA includes a polymorphism that results in an upstream start codon in some individuals

Integrin beta-5 acts as a receptor for adenovirus type C

Serine/threonine protein kinase which enhances GLI1 and GLI2 transcriptional activity and consequently positively regulates GLI-dependent SHH signaling

p56Dok-2(Phospho-Tyr351) Rabbit Polyclonal Antibody, 100ul Sampling Tubes Mutations in this gene resultThe protein encoded by this gene is constitutively tyrosine phosphorylated in hematopoietic progenitors isolated from chronic myelogenous leukemia (CML) patients in the chronic phase. It may be a critical substrate for p210(bcr abl) a chimeric protein whose presence is associated with CML. This encoded protein binds p120 (RasGAP) from CML cells.