CEP68 Polyclonal Antibody, 100ul Pipette Controller A mutation in this gene

A mutation in this gene has been associated with bilateral nasolacrimal duct obstruction (LCDD)

22µm pore size and a 50mm diameter

however| the expression pattern suggests a role in lipid homeostasis in cells of the immune system

The solute carrier family 9 member A6 localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume

An important paralog of C1R is HP

CEP68 Polyclonal Antibody, 100ul Pipette Controller A mutation in this geneCEP68 (Centrosomal Protein 68) is a Protein Coding gene. Diseases associated with CEP68 include Retinitis Pigmentosa 28. Involved in maintenance of centrosome cohesion, probably as part of a linker structure which prevents centrosome splitting (PubMed: 18042621). Required for localization of CDK5RAP2 to the centrosome during interphase.