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

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 (17) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
SLC35A3 229782 Q8R1T4
SLC35A3 23443 Q9Y2D2
Rat SLC35A3 SLC35A3 310808 Q6AXR5
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Top Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 Proteins at antibodies-online.com

Showing 3 out of 4 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
Insect Cells Mouse rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Log in to see 49 to 54 Days
$4,244.78
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Insect Cells Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Log in to see 49 to 54 Days
$6,041.49
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HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
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SLC35A3 Proteins by Origin and Source

Origin Expressed in Conjugate
Mouse (Murine)

Human ,
,

More Proteins for Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 (SLC35A3) Interaction Partners

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

  1. UDP-galactose (show B4GALT1 Proteins) (SLC35A2 (show SLC35A2 Proteins)) and UDP-N-acetylglucosamine (show MGAT4B Proteins) (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 Proteins) and NGT cooperate in the UDP-Gal (show B4GALT1 Proteins) 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) Protein Profile

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

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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