ARMCX2 Polyclonal Antibody, 20ul Contamination Detection & Removal With 50 units/μL activity and

With 50 units/μL activity and a convenient 200 μL size

The human genome contains related pseudogenes

Mutations in APP have been implicated in autosomal dominant Alzheimer disease and cerebroarterial amyloidosis (cerebral amyloid angiopathy)

Mutations in the promoter region of this gene lead to a diminished response to antileukotriene drugs used in the treatment of asthma and may also be associated with atherosclerosis and several cancers

The human genome contains several non-transcribed pseudogenes of SLC25A6

ARMCX2 Polyclonal Antibody, 20ul Contamination Detection & Removal With 50 units/μL activity andARMCX2 encodes a protein (armadillo repeat containing, X linked 2) containing a potential N terminal transmembrane domain and multiple armadillo (arm) repeats. Proteins containing arm repeats are involved in development, maintenance of tissue integrity, and tumorigenesis. ARMCX2 is located in a cluster of related genes on chromosome X. There is a pseudogene for ARMCX2 on chromosome 7. Alternative splicing in the 5' UTR results in multiple transcript