FANCD2(Phospho Ser222) Polyclonal Antibody, 50ul Cell Culture Plates a member of the CC-chemokine

a member of the CC-chemokine family

Mutations in this gene cause VLDLR-associated cerebellar hypoplasia

ADIPOQ is expressed in adipose tissue exclusively

This gene is closely linked to related family member T-box 3 (ulnar mammary syndrome) on human chromosome 12

Epidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun-exposed skin

FANCD2(Phospho Ser222) Polyclonal Antibody, 50ul Cell Culture Plates a member of the CC-chemokineThe 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