Anti-Human/Mouse SLC9A9 Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA05285
Size 100μl
Host Type Rabbit
Immunogen Synthesized peptide derived from the Internal region of human NHE-9
Specificity Ubiquitously expressed in all tissues tested. Expressed at highest levels in heart and skeletal muscle, followed by placenta, kidney, and liver. Expressed in the brain, in the medulla and spinal cord.
Isotype IgG
Reacitivity Human,Mouse
Clone
Uniprot Q8IVB4
Concentration 1mg/mL
Dilution WB 1:500-1:2000, ELISA 1:40000
Formulation
Application WB,ELISA
Other Names 5730527A11Rik,9930105B05,AI854429,FLJ35613,Na(+)/H(+) exchanger 9,Nbla00118,NHE 9,NHE-9,NHE9,Putative protein product of Nbla00118,SL9A9,Slc9a9,Sodium/hydrogen exchanger 9,Sodium/proton exchanger NHE9,Solute carrier family 9 (sodium/hydrogen exchanger) isoform 9,Solute carrier family 9 (sodium/hydrogen exchanger) member 9,Solute carrier family 9 member 9
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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