Anti-Human 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 PA08083
Size 100μl
Host Type Rabbit
Immunogen Synthetic peptide of human SLC9A9
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
Clone
Uniprot Q8IVB4
Concentration 0.7 mg/mL
Dilution IHC 1:25-1:100
Formulation
Application IHC,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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