SLC12A9 Antibodies

AND SLC12A9 ELISA kits, SLC12A9 Proteins

Many biological assays use antibodies to detect SLC12A9, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with SLC12A9 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop SLC12A9 antibodies...

We validate the specificity of these antibodies to SLC12A9 by testing them on tissues known to express SLC12A9 positively and negatively. Browse below to find the SLC12A9 antibody that suites your experiment. We have 0 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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SLC12A9 Infographic by Boster Bio

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SLC12A9 Overview

Facts about Solute carrier family 12 member 9.

SLC12A9 3D structure. Source: alphafold

Solute carrier family 12 member 9 (SLC12A9)

May be an inhibitor of SLC12A1.
Seems to correspond to a subunit of a multimeric transport system and thus, additional subunits might be required for its purpose.

Gene Information

Human
Gene Name:	SLC12A9
Uniprot:	Q9BXP2
Entrez:	56996

Family

Belongs to:

SLC12A transporter family

Alternative Names

Solute carrier family 12 member 9

Molecular Weight

Mass (kDA):
96.11 kDA

Genomic Context


Human

Location:	7q22.1
Sequence:	7; NC_000007.14 (100826869..100867012)

Tissue Specificity

Highly expressed in placenta, brain and kidney. Lower expression in lung, liver and heart.

Subcellular Localizations

Cell membrane; Multi-pass membrane protein.

PTMs

Glycoprotein

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SLC12A9

References

PMID: 10871601 by Caron L., et al. Cloning and functional characterization of a cation-Cl-cotransporter- interacting protein.

PMID: 11239002 by Wilson M.D., et al. Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5.