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Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 (SLC35A3) ELISA Kits

SLC35A3 encodes a UDP-N-acetylglucosamine transporter found in the golgi apparatus membrane. Additionally we are shipping Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 Antibodies (16) and Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 Proteins (4) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Mouse SLC35A3 SLC35A3 229782 Q8R1T4
Anti-Human SLC35A3 SLC35A3 23443 Q9Y2D2
Anti-Rat SLC35A3 SLC35A3 310808 Q6AXR5
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More ELISA Kits for Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 Interaction Partners

Human Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 (SLC35A3) interaction partners

  1. UDP-galactose (show B4GALT1 ELISA Kits) (SLC35A2 (show SLC35A2 ELISA Kits)) and UDP-N-acetylglucosamine (show MGAT4B ELISA Kits) (SLC35A3) Transporters Form Glycosylation-related Complexes with Mannoside Acetylglucosaminyltransferases (Mgats).

  2. Identified deleterious mutations in SLC35A3 in eight patients from a large kindred, who suffered from autism spectrum disorder, arthrogryposis and epilepsy.

  3. The data further supports the hypothesis that UGT (show SLC35A2 ELISA Kits) and NGT cooperate in the UDP-Gal (show B4GALT1 ELISA Kits) delivery for glycosyltransferases located in the Golgi apparatus.

  4. A mutation in the SLC35A3 gene is associated with vertebral malformations in cattle. A missense mutation likely effects signal transduction which relies on glycosylation.

  5. SLC35A3 is an unlikely candidate for the pathogenesis of vertebral malformations because no mutation was found in this cohort study.

Cow (Bovine) Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 (SLC35A3) interaction partners

  1. A defective SLC35A3 gene is associated with severe axial skeletal deformities, symmetric arthrogryposis of the lower limb joints, craniofacial dysmorphism, and cardiac anomalies.

Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 (SLC35A3) Antigen Profile

Antigen Summary

This gene encodes a UDP-N-acetylglucosamine transporter found in the golgi apparatus membrane. In cattle, a missense mutation in this gene causes complex vertebral malformation. Alternative splicing results in multiple transcript variants.

Gene names and symbols associated with SLC35A3

  • solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 (Slc35a3) antibody
  • solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member A3 (SLC35A3) antibody
  • solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member A3 (Slc35a3) antibody
  • 2310050P13Rik antibody

Protein level used designations for SLC35A3

UDP-N-acetylglucosamine transporter , golgi UDP-GlcNAc transporter , solute carrier family 35 member A3 , solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 , UDP N-acetylglucosamine transporter , solute carrier family 35 member 3

GENE ID SPECIES
229782 Mus musculus
23443 Homo sapiens
442991 Canis lupus familiaris
520918 Bos taurus
310808 Rattus norvegicus
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