NHE-9 rabbit pAb

• Background :

  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]

• Description :

  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],

• Product Name Alternative :

  SLC9A9; NHE9; Nbla00118; Sodium/hydrogen exchanger 9; Na (+) /H (+) exchanger 9; NHE-9; Solute carrier family 9 member 9

• UniProt :

  Q8IVB4

• Swiss Prot :

  Q8IVB4

• Reactivity :

  Human; Mouse

• Immunogen :

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

• Target :

  NHE-9

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB; ELISA

• Concentration :

  1 mg/ml

• Dilution :

  Western Blot: 1/500 - 1/2000. ELISA: 1/40000. Not yet tested in other applications.

• Buffer :

  -20°C/1 year

• Molecular Weight :

  65kD

• Storage Conditions :

  -20°C/1 year

• Observed Molecular Weight :

  65kD

• Fragment :

  IgG

• Subcellular Location :

  Late endosome membrane ; Multi-pass membrane protein .

• Other Product Names :

  SLC9A9; NHE9; Nbla00118; Sodium/hydrogen exchanger 9; Na (+) /H (+) exchanger 9; NHE-9; Solute carrier family 9 member 9

• Gene ID (Human) :

  285195