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技术规格
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.
Applications:
ELISA, IHC
Name of antibody:
SLC9A9
Immunogen:
Synthetic peptide of human SLC9A9
Full name:
solute carrier family 9, subfamily A (NHE9, cation proton antiporter 9), member 9
Synonyms:
NHE9; AUTS16
SwissProt:
Q8IVB4
ELISA Recommended dilution:
1000-2000
IHC positive control:
Human breast cancer
IHC Recommend dilution:
25-100