SL9A3 Polyclonal Antibody, 20ul Cell Culture & Maintenance with identical protein backbones but

with identical protein backbones but different glycosylation profiles

Mutations in this gene may underlie hereditary disorders of balance and hearing

Diseases associated with PRAF2 include neuroblastoma

As the sequence environment of the 2 potential ATG initiator codons is the same for the other altrnatively spliced isoforms| alternative initiation of translation could also occur on these transcripts

SL9A3 Polyclonal Antibody, 20ul Cell Culture & Maintenance with identical protein backbones butThe protein encoded by this gene is an epithelial brush border Na H exchanger that uses an inward sodium ion gradient to expel acids from the cell. Defects in this gene are a cause of congenital secretory sodium diarrhea. Pseudogenes of this gene exist on chromosomes 10 and 22.