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Browse our anti-SLC26A2 (SLC26A2) Antibodies

Full name:
anti-Solute Carrier Family 26 (Sulfate Transporter), Member 2 Antibodies (SLC26A2)
On www.antibodies-online.com are 18 Solute Carrier Family 26 (Sulfate Transporter), Member 2 (SLC26A2) Antibodies from 9 different suppliers available. Additionally we are shipping SLC26A2 Proteins (5) and many more products for this protein. A total of 26 SLC26A2 products are currently listed.
Synonyms:
D5S1708, Dtd, Dtdst, EDM4, MST153, MSTP157, SLC26A2, ST-OB
list all antibodies Gene Name GeneID UniProt
SLC26A2 1836 P50443
SLC26A2 117267 O70531
SLC26A2 13521 Q62273

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anti-Mouse (Murine) SLC26A2 Antibodies:

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Top referenced anti-SLC26A2 Antibodies

  1. Human Monoclonal SLC26A2 Primary Antibody for ELISA, WB - ABIN515087 : Yusa, Miyazaki, Kimura, Izawa, Kannagi: Epigenetic silencing of the sulfate transporter gene DTDST induces sialyl Lewisx expression and accelerates proliferation of colon cancer cells. in Cancer research 2010 (PubMed)

More Antibodies against SLC26A2 Interaction Partners

Human Solute Carrier Family 26 (Sulfate Transporter), Member 2 (SLC26A2) interaction partners

  1. slc26a2 is to be a critical otic gene whose dysfunction may induce hearing impairment

  2. findings provide the first identification of autosomal dominant SLC26A2 mutations in patients with dysplastic spondylolysis, suggesting a new clinical entity in the pathogenesis of chondrodysplasia (show COL11A1 Antibodies) involving lumbosacral spine

  3. Diastrophic dysplasia sulfate transporter (SLC26A2) is expressed in the adrenal cortex and regulates aldosterone secretion.

  4. Up-regulation of SLC26A2 is associated with colorectal cancer.

  5. A compound heterozygote SLC26A2 mutation is associated with robin sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia

  6. SLC13A4 (show SLC13A4 Antibodies) and SLC26A2 were the most abundant sulfate transporter mRNAs, which localized to syncytiotrophoblast and cytotrophoblast cells, respectively.

  7. 73% of autosomal-recessive multiple epiphyseal dysplasia patients were either homozygous, or compound heterozygous, for SLC26A2 mutations.

  8. Solute carrier (show SERTAD2 Antibodies) family 26 member a2 (Slc26a2) protein functions as an electroneutral SOFormula/OH-/Cl- exchanger regulated b

  9. Mutations in the SLC26A2 gene causes diastrophic dysplasia.

  10. Analysis suggests that, while the DTDST family of disorders contains at least seven different conditions, gene mutations appear to cause a phenotypic continuum. DTDST genotype alone is an imperfect predictor of clinical severity along this continuum.

Mouse (Murine) Solute Carrier Family 26 (Sulfate Transporter), Member 2 (SLC26A2) interaction partners

  1. Diastrophic dysplasia sulfate transporter (SLC26A2) is expressed in the adrenal cortex and regulates aldosterone secretion.

  2. These findings reveal multiple roles for Slc26a2 in chondrocyte biology and emphasize the importance of Slc26a2-mediated protein sulfation in cell signaling

  3. a Slc26a2 mutation results in matrix disruptions, growth, and degradation of cartilage with impaired sulfation

  4. Characterize transport of oxalate and sulfate by human SLC26A2 and mouse Slc26a2 expressed in Xenopus oocytes.

  5. Homozygous mutant mice for SLC26A2 were characterized by skeletal dysplasia with chondrocytes of irregular size, delay in the formation of the secondary ossification centre and osteoporosis of long bones.

Cow (Bovine) Solute Carrier Family 26 (Sulfate Transporter), Member 2 (SLC26A2) interaction partners

  1. Sheep, goat and cattle R-banded chromosome preps, obtained from synchronized cell cultures, were used to FISH-map leptin (show LEP Antibodies) and SLC26A2 genes on single chromosome bands. SLC26A2 maps on BTA7q24, OAR5q24 and CHI7q24.

SLC26A2 Antigen Profile

Antigen Summary

The diastrophic dysplasia sulfate transporter is a transmembrane glycoprotein implicated in the pathogenesis of several human chondrodysplasias. It apparently is critical in cartilage for sulfation of proteoglycans and matrix organization.

Alternative names and synonyms associated with SLC26A2

  • solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) antibody
  • solute carrier family 26 (sulfate transporter), member 2 (slc26a2) antibody
  • solute carrier family 26 (anion exchanger), member 2 (SLC26A2) antibody
  • solute carrier family 26 (anion exchanger), member 2 (Slc26a2) antibody
  • solute carrier family 26 (sulfate transporter), member 2 (Slc26a2) antibody
  • D5S1708 antibody
  • Dtd antibody
  • Dtdst antibody
  • EDM4 antibody
  • MST153 antibody
  • MSTP157 antibody
  • SLC26A2 antibody
  • ST-OB antibody

Protein level used designations for SLC26A2

solute carrier family 26 (sulfate transporter), member 2 , sulfate transporter-like , diastrophic dysplasia protein , sulfate anion transporter 1 , sulfate transporter , diastrophic dysplasia protein homolog , solute carrier family 26 member 2 , DTD sulfate transporter , Sulfate transporter , solute carrier protein 26a2 , Solute carrier family 26 member 2

GENE ID SPECIES
427611 Gallus gallus
612273 Canis lupus familiaris
709998 Macaca mulatta
100028865 Monodelphis domestica
100388764 Callithrix jacchus
100461101 Pongo abelii
100544098 Meleagris gallopavo
100556372 Anolis carolinensis
1836 Homo sapiens
117267 Rattus norvegicus
13521 Mus musculus
513953 Bos taurus
100034141 Equus caballus
100294558 Ovis aries
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