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Mouse solute carrier family 26 (sulfate transporter) , member 2 ELISA Kit | SLC26A2 elisa kit

Mouse Sulfate transporter, SLC26A2 ELISA Kit

Gene Names
Slc26a2; Dtd; ST-OB
Reactivity
Mouse
Synonyms
solute carrier family 26 (sulfate transporter); member 2; Mouse Sulfate transporter; SLC26A2 ELISA Kit; Mouse Sulfate transporter (SLC26A2) ELISA kit; D5S1708; DTD; DTDST; EDM4; MST153; MSTP157; diastrophic dysplasia sulfate transporter; solute carrier family 26 member 2; sulfate anion transporter 1; SLC26A2 elisa kit
Ordering
For Research Use Only!
Reactivity
Mouse
Preparation and Storage
Store all reagents at 2-8 degree C

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
81,604 Da
NCBI Official Full Name
sulfate transporter
NCBI Official Synonym Full Names
solute carrier family 26 (sulfate transporter), member 2
NCBI Official Symbol
Slc26a2
NCBI Official Synonym Symbols
Dtd; ST-OB
NCBI Protein Information
sulfate transporter; solute carrier family 26 member 2; diastrophic dysplasia protein homolog
UniProt Protein Name
Sulfate transporter
Protein Family
UniProt Gene Name
Slc26a2
UniProt Synonym Gene Names
Dtd; Dtdst
UniProt Entry Name
S26A2_MOUSE

Uniprot Description

SLC26A2: Sulfate transporter. May play a role in endochondral bone formation. Defects in SLC26A2 are the cause of diastrophic dysplasia (DTD). DTD is an autosomal recessive disease characterized by osteochondrodysplasia with clinical features including dwarfism, spinal deformation, and specific joint abnormalities. Defects in SLC26A2 are the cause of achondrogenesis type 1B (ACG1B). ACG1B is a recessively inherited chondrodysplasia characterized by extremely poor skeletal development and perinatal death. Defects in SLC26A2 are the cause of atelosteogenesis type 2 (AO2); also known as neonatal osseous dysplasia 1. AO2 is characterized by severely shortened limbs, small chest, scoliosis, club foot of the equinovarus type (talipes equinovarus), abducted thumbs and great toes, and cleft palate. Patients die of respiratory insufficiency shortly after birth because of the collapse of the airways and pulmonary hypoplasia due to the small rib cage. Defects in SLC26A2 are the cause of multiple epiphyseal dysplasia type 4 (EDM4). EDM is a generalized skeletal dysplasia associated with significant morbidity. Joint pain, joint deformity, waddling gait, and short stature are the main clinical signs and symptoms. EDM is broadly categorized into the more severe Fairbank and the milder Ribbing types. EDM4 is a recessively inherited form, characterized by early childhood-onset hip dysplasia and recurrent patella dislocation. Short stature in EDM4 patients is not frequent. Belongs to the SLC26A/SulP transporter (TC 2.A.53) family.

Protein type: Transporter, SLC family; Transporter; Membrane protein, integral; Membrane protein, multi-pass

Cellular Component: membrane; integral to membrane

Molecular Function: sulfate transmembrane transporter activity; secondary active sulfate transmembrane transporter activity

Biological Process: ossification; transport; sulfate transport; ion transport; transmembrane transport

Research Articles on SLC26A2

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Product Notes

The Mouse SLC26A2 slc26a2 (Catalog #AAA9329549) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA9329549 ELISA Kit recognizes Mouse SLC26A2. It is sometimes possible for the material contained within the vial of "solute carrier family 26 (sulfate transporter) , member 2, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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