SLC9A9 Antibodies

AND SLC9A9 ELISA kits, SLC9A9 Proteins

Many biological assays use antibodies to detect SLC9A9, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with SLC9A9 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop SLC9A9 antibodies...

We validate the specificity of these antibodies to SLC9A9 by testing them on tissues known to express SLC9A9 positively and negatively. Browse below to find the SLC9A9 antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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SLC9A9 Infographic by Boster Bio

All SLC9A9 Products

Product

Figures

Specificity

Applications

Price

Anti-NHE-9 SLC9A9 Antibody

5 Q&As

Human, Mouse

ELISA, WB

$399
Cat # A05959-1
100μl

SLC9A9 Overview

Facts about Sodium/hydrogen exchanger 9.

SLC9A9 3D structure. Source: alphafold

Sodium/hydrogen exchanger 9 (SLC9A9)

May act in electroneutral exchange of protons for Na(+) across membranes. Involved from the effusion of Golgi luminal H(+) in exchange for cytosolic cations.

Involved in organelle ion homeostasis by contributing to the maintenance of the distinctive acidic pH values of the Golgi and post-Golgi compartments in the cell. .

Gene Information

Human
Gene Name:	SLC9A9
Uniprot:	Q8IVB4
Entrez:	285195

Family

Belongs to:

monovalent cation:proton antiporter 1 (CPA1) transporter (TC 2.A.36) family

Alternative Names

AUTS16; FLJ35613; Na(+)/H(+) exchanger 9; NHE9; NHE-9; putative protein product of Nbla00118; sodium/hydrogen exchanger 9; sodium/proton exchanger NHE9; solute carrier family 9 (sodium/hydrogen exchanger); solute carrier family 9 (sodium/hydrogen exchanger), isoform 9; solute carrier family 9 (sodium/hydrogen exchanger), member 9; Solute carrier family 9 member 9

Molecular Weight

Mass (kDA):
72.565 kDA

Genomic Context


Human

Location:	3q24
Sequence:	3; NC_000003.12 (143265222..143848492, complement)

Tissue 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.

Subcellular Localizations

Late endosome membrane; Multi-pass membrane protein.

Diseases

Attention Deficit Hyperactivity Disorder
Malnutrition
Autistic Disorder
Mental Disorders
Dysequilibrium Syndrome
Malignant Squamous Cell Neoplasm
Tissue Adhesions
Chromosome Inversion
Carcinoma

Substance Use Disorder
Squamous Cell Carcinoma Of Esophagus
Esophageal Neoplasms

Interacting Proteins

ZDHHC17

Pathways

Protein Phosphorylation
Cell Division
Glycosylation
Synaptic Transmission
Regulation Of Gene Expression
Pathogenesis

Cytokinesis

PTMs

Glycosylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SLC9A9

References

PMID: 14569117 by De Silva M.G., et al. Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype.

PMID: 15522866 by Nakamura N., et al. Four Na+/H+ exchanger isoforms are distributed to Golgi and post- Golgi Compartments and are involved in organelle pH regulation.