FANCD2 Polyclonal Antibody, 20ul Micro Centrifuge Tubes Mutations in SPTAN1 are the

Mutations in SPTAN1 are the cause of early infantile epileptic encephalopathy-5

The translation initiation factor EIF2 catalyzes the first regulated step of protein synthesis initiation

This apolipoprotein L family member may play a role in lipid exchange and transport throughout the body

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FANCD2 Polyclonal Antibody, 20ul Micro Centrifuge Tubes Mutations in SPTAN1 are theThe 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