FANCA Polyclonal Antibody, 100ul Centrifuges Mutations in this gene have

Mutations in this gene have be associated glycogen storage disease

The product of this gene catalyzes sulfonation by transferring a sulfate group to the 3' position of galactose in N-acetyllactosamine in both type 2 (Gal-beta-1-4GlcNAc-R) oligosaccharides and core-2-branched O-glycans| but not on type 1 or core-1-branched structures

Interacts with PPP6C

as well as X-linked combined immunodeficiency (XCID)

Made of high-quality PET/PS with excellent chemical stability Available in various specifications

FANCA Polyclonal Antibody, 100ul Centrifuges Mutations in this gene haveThe Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal