FANCA Polyclonal Antibody, 50ul sgRNA customized design CDK11B shares very high sequence

CDK11B shares very high sequence identity with a neighboring gene

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

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

2000 [PubMed 10799485])

this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function

FANCA Polyclonal Antibody, 50ul sgRNA customized design CDK11B shares very high sequenceThe 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