NHE-9 rabbit pAb
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 Specifications
Background
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
Available Sizes
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