FANCA Polyclonal Antibody, 50ul sgRNA customized design Me2SO and PMA treatment in

Me2SO and PMA treatment in differentiating myeloid leukemia cells

Mutations in this gene are associated with ectodermal dysplasia| and cleft lip/palate syndrome 3 (EEC3)

Haploinsufficiency of this protein can cause maternal riboflavin deficiency

SYT11 is a member of the synaptotagmin gene family and encodes Synaptotagmin-11 similar to other family members that are known calcium sensors and mediate calcium-dependent regulation of membrane trafficking in synaptic transmission

This enzyme highly contributes to the antioxidant defense system

FANCA Polyclonal Antibody, 50ul sgRNA customized design Me2SO and PMA treatment inThe 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