NHE-9 Polyclonal Antibody

Background:
solute carrier family 9 member A9(SLC9A9) Homo sapiens This gene encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. The encoded protein localizes the to the late recycling endosomes and may play an important role in maintaining cation homeostasis. Mutations in this gene are associated with autism susceptibility 16 and attention-deficit/hyperactivity disorder. [provided by RefSeq, Mar 2012],

Alternative Names:
SLC9A9, NHE9, Nbla00118, Sodium/hydrogen exchanger 9, Na(+)/H(+) exchanger 9, NHE-9, Solute carrier family 9 member 9

Immunogen: The antiserum was produced against synthesized peptide derived from human SLC9A9. AA range:171-220

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

Observed band: 65

GeneID: SLC9A9

Storage: -20°C/1 year

NOTE: For Research Use Only