FANCD2 Polyclonal Antibody, 20ul Micro Centrifuge Tubes and neurodegenerative disorders

and neurodegenerative disorders

Multiple alternatively spliced transcript variants encoding several different isoforms have been found for this gene

making it ideal for various laboratory applications

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

1- 100 mL)

FANCD2 Polyclonal Antibody, 20ul Micro Centrifuge Tubes and neurodegenerative disordersThe 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