Barttin Antibodies

AND BSND ELISA kits, Barttin Proteins

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

We validate the specificity of these antibodies to Barttin by testing them on tissues known to express BSND positively and negatively. Browse below to find the BSND antibody that suites your experiment. We have 3 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.

Previous: CBLIF Next: DAP3

BSND Infographic by Boster Bio

All BSND Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-Barttin BSND Antibody

Western blot analysis of extracts of various cell lines, using BSND antibody at 1:1000 dilution

Human, Mouse, Rat

$405
Cat # A09766
100ul

Human BSND Recombinant Protein

SDS-PAGE

$281
Cat # PROTQ8WZ55
Starting from 10ug

BSND (NM_057176) Human Over-expression Lysate

Human

$628
Cat # LS007809
20 µg, 100 µg

BSND Overview

Facts about Barttin.

BSND 3D structure. Source: alphafold

Barttin (BSND)

Functions as a beta-subunit for CLCNKA and CLCNKB chloride channels.
From the kidney CLCNK/BSND heteromers mediate chloride reabsorption by facilitating its basolateral efflux.

From the stria, CLCNK/BSND stations drive potassium secretion by recycling chloride for the basolateral SLC12A2 cotransporter. .

Gene Information

Human
Gene Name:	BSND
Uniprot:	Q8WZ55
Entrez:	7809

Family

Belongs to:

No superfamily

Alternative Names

BARTMGC119284; Bartter syndrome, infantile, with sensorineural deafness (Barttin); barttin; deafness, autosomal recessive 73; DFNB73; MGC119283; MGC119285

Molecular Weight

Mass (kDA):
35.197 kDA

Genomic Context


Human

Location:	1p32.3
Sequence:	1; NC_000001.11 (54998933..55017172)

Tissue Specificity

Expressed primarily in kidney. Expressed in specific nephron segments and in the stria vascularis of the inner ear.

Subcellular Localizations

Cell membrane; Multi-pass membrane protein. Cytoplasm. A significant amount also observed intracellularly. Staining in membranes of the renal tubule and of potassium-secreting epithelia of the inner ear is basolateral (By similarity).

Diseases

Bartter Disease
Complete Hearing Loss
Sensorineural Hearing Loss (disorder)
Hypertensive Disease
Alkalosis
Metabolic Alkalosis
Kidney Failure
Kidney Diseases
Gitelman Syndrome
Kidney Failure, Chronic
Polyhydramnios
Diabetes Mellitus

Deafness Congenital
Hypercalciuria
Hyperaldosteronism
Polyuria
Dehydration
Nephrogenic Diabetes Insipidus

Pathways

Transport
Chloride Transport
Localization
Pathogenesis
Secretion
Glomerular Filtration
Water Homeostasis
Transepithelial Chloride Transport
Excretion
Renal Water Homeostasis
Membrane Hyperpolarization
Anion Transport
Endocytosis

Transepithelial Transport
Regulation Of Transport
Membrane Depolarization
Translation
Cellular Localization
Acid Secretion
Regulation Of Blood Pressure

PTMs

Phosphorylation

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

References

PMID: 11687798 by Birkenhaeger R., et al. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure.

PMID: 11734858 by Estevez R., et al. Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion.