Sulfate transporter Antibodies

AND SLC26A2 ELISA kits, Sulfate transporter Proteins

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

We validate the specificity of these antibodies to Sulfate transporter by testing them on tissues known to express SLC26A2 positively and negatively. Browse below to find the SLC26A2 antibody that suites your experiment. We have 2 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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SLC26A2 Infographic by Boster Bio

All SLC26A2 Products

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Specificity

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Price

Anti-Sulfate transporter SLC26A2 Antibody

Human, Mouse, Rat

$405
Cat # A04631
100ul

SLC26A2 (NM_000112) Human Over-expression Lysate

Human

$628
Cat # LS001836
100 µg

SLC26A2 Overview

Facts about Sulfate transporter.

SLC26A2 3D structure. Source: alphafold

Sulfate transporter (SLC26A2)

Sulfate transporter. May play a role in endochondral bone formation.

Gene Information

Human
Gene Name:	SLC26A2
Uniprot:	P50443
Entrez:	1836

Family

Belongs to:

SLC26A/SulP transporter (TC 2.A.53) family

Alternative Names

D5S1708; Diastrophic dysplasia protein; diastrophic dysplasia sulfate transporter; DTDMSTP157; DTDSTMST153; EDM4; solute carrier family 26 (sulfate transporter), member 2; Solute carrier family 26 member 2; sulfate anion transporter 1; sulfate transporter

Molecular Weight

Mass (kDA):
81.662 kDA

Genomic Context


Human

Location:	5q32
Sequence:	5; NC_000005.10 (149960758..149987400)

Tissue Specificity

Ubiquitously expressed.

Subcellular Localizations

Cell membrane; Multi-pass membrane protein.

Diseases

Dysplasia
Diastrophic Dysplasia
Osteochondrodysplasias
Multiple Epiphyseal Dysplasia
Atelosteogenesis
Achondrogenesis, Type Ib (disorder)
Bone Diseases, Developmental
Skeletal Dysplasia
Dwarfism
Achondroplasia
Pendred's Syndrome

Diarrhea
Complete Hearing Loss
Congenital Abnormality
Fetal Diseases
Congenital Clubfoot

Pathways

Transport
Sulfation
Sulfate Transport
Ossification
Localization
Secretion
Anion Transport
Oxalate Transport
Chondrocyte Differentiation
Translation
Endochondral Ossification
Osteoblast Differentiation

Ion Transport
Chondrocyte Proliferation
Cell Differentiation
Bone Remodeling
Bone Development
Pathogenesis
Acid Secretion

PTMs

Sulphation

Glycosylation

Oxidation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SLC26A2

References

PMID: 7923357 by Haestbacka J., et al. The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping.

PMID: 8528239 by Superti-Furga A., et al. Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene.