FANCD2(Phospho Ser222) Polyclonal Antibody, 50ul Cell Culture Plates Mutations in this gene cause

Mutations in this gene cause VLDLR-associated cerebellar hypoplasia

The functioning of this gene is implicated in a wide variety of inflammation-associated disease states

ADIPOQ is expressed in adipose tissue exclusively

NMDA receptor channels are heteromers composed of three different subunits: NR1 (GRIN1)

It is not currently known whether the encoded protein is a functional ribosomal protein or whether it has evolved a function that is independent of the ribosome

FANCD2(Phospho Ser222) Polyclonal Antibody, 50ul Cell Culture Plates Mutations in this gene causeThe 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