anti-CMP-Sialic Acid Transporter (CMPST) Anticorps

The protein encoded by CMPST is found in the membrane of the Golgi apparatus, where it transports nucleotide sugars into the Golgi. De plus, nous expédions CMP-Sialic Acid Transporter Kits (4) et CMP-Sialic Acid Transporter Protéines (3) et beaucoup plus de produits pour cette protéine.

afficher tous les anticorps Gène GeneID UniProt
CMPST 24060 Q61420
CMPST 10559 P78382
CMPST 313139  
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Top anti-CMP-Sialic Acid Transporter Anticorps sur anticorps-enligne.fr

Showing 3 out of 6 products:

Catalogue No. Reactivité Hôte Conjugué Application Images Quantité Livraison Prix Détails
Humain Lapin Inconjugué ELISA, IHC   100 μL 11 to 16 Days
$454.83
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Humain Lapin Inconjugué ELISA, IHC   50 μL 11 to 16 Days
$412.19
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Humain Lapin Inconjugué IHC, ELISA   50 μL 9 to 11 Days
$483.57
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Plus d’anticorps contre CMP-Sialic Acid Transporter partenaires d’interaction

Mouse (Murine) CMP-Sialic Acid Transporter (CMPST) interaction partners

  1. CMP-sialic acid transporter is localized in the medial-trans Golgi

  2. analysis of the functional murine CMP-sialic acid transporter expressed in the E. coli inner membrane

Human CMP-Sialic Acid Transporter (CMPST) interaction partners

  1. We performed exome sequencing on an individual with a profound neurological presentation and identified rare compound heterozygous mutations, p.Thr156Arg and p.Glu196Lys, in the CMP-sialic acid transporter, SLC35A1. Patient primary fibroblasts and serum showed a considerable decrease in the amount of N- and O-glycans terminating in sialic acid

  2. the SLC35A1 generates additional isoforms through alternative splicing.

  3. SLC35A1-deficient cells lack of alpha-dystroglycan O-mannosylation, ligand binding and incorporation of sialic acids.

  4. We confirm an autosomal recessive, generalized sialylation defect due to mutations in SLC35A1

  5. substrate binding specificity

  6. this defect is a new type of congenital disorder of glycosylation (CDG) of type IIf affecting the transport of CMP-sialic acid into the Golgi apparatus.

  7. this study, we introduced two critical genes encoding human CMP-N-acetylneuraminic acid synthetase and CMP-sialic acid transporter into tobacco suspension-cultured cell to pave a route for sialic biosynthetic pathway.

  8. CMP-sialic acid transporter is localized in the medial-trans Golgi

CMP-Sialic Acid Transporter (CMPST) profil antigène

Profil protéine

The protein encoded by this gene is found in the membrane of the Golgi apparatus, where it transports nucleotide sugars into the Golgi. One such nucleotide sugar is CMP-sialic acid, which is imported into the Golgi by the encoded protein and subsequently glycosylated. Defects in this gene are a cause of congenital disorder of glycosylation type 2F (CDG2F). Two transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with CMPST

  • solute carrier family 35 (CMP-sialic acid transporter), member 1 (Slc35a1) anticorps
  • solute carrier family 35 member A1 (Slc35a1) anticorps
  • solute carrier family 35 member A1 (SLC35A1) anticorps
  • AA408150 anticorps
  • AI314851 anticorps
  • CDG2F anticorps
  • CMP-SA-Tr anticorps
  • CMP-Sia-Tr anticorps
  • CMPST anticorps
  • CST anticorps
  • hCST anticorps

Protein level used designations for CMPST

CMP-SA-Tr , CMP-Sia-Tr , CMP-sialic acid transporter , solute carrier family 35 member A1 , Solute carrier family 35 member A1 , mutated CMP-sialic acid transporter A1 , solute carrier family 35 (CMP-sialic acid transporter), member 1 , solute carrier family 35 (UDP-galactose transporter), member 1

GENE ID SPECIES
24060 Mus musculus
100689322 Cricetulus griseus
10559 Homo sapiens
313139 Rattus norvegicus
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