beta 1,3-Galactosyltransferase-Like (B3GALTL) ELISA Kits

The protein encoded by B3GALTL is a beta-1,3-glucosyltransferase that transfers glucose to O-linked fucosylglycans on thrombospondin type-1 repeats (TSRs) of several proteins. Zusätzlich bieten wir Ihnen B3GALTL Antikörper (21) und B3GALTL Proteine (7) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
B3GALTL 145173 Q6Y288
Anti-Maus B3GALTL B3GALTL 381694 Q8BHT6
B3GALTL    
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Top B3GALTL ELISA Kits auf antikoerper-online.de

Showing 10 out of 11 products:

Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Anbieter Lieferzeit Preis Details
Ratte 0.1 ng/mL 5.0-100 ng/mL   96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
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Human
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
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Huhn
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
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Schaf
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
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Meerschweinchen
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
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Schwein
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
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Kaninchen
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
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Hund
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
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Ziege
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
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Affe
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
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Weitere ELISA Kits für B3GALTL Interaktionspartner

Human beta 1,3-Galactosyltransferase-Like (B3GALTL) Interaktionspartner

  1. POFUT2 (zeige POFUT2 ELISA Kits) and B3GLCT mediate a noncanonical endoplasmic reticulum quality-control mechanism that recognizes folded thrombospondin type 1 repeats and stabilizes them by glycosylation.

  2. Mutations in the coding region of B3GALTL were identified in nine patients; six had a documented phenotype of classic Peters plus syndrome (PPS) and the remaining three had a clinical diagnosis of PPS with incomplete clinical documentation.

  3. a novel c.597-2 A>G splicing mutation within the B3GALTL gene in typical Peters-plus syndrome

  4. A novel homozygous c.597-2A>G mutation was identified in both patients with Peters plus syndrome harbouring a novel splice site mutation in the B3GALTL gene

  5. Vertebral defects in a patient with Peters plus syndrome and mutations in B3GALTL.

  6. The present report confirms the wide clinical spectrum of Peters plus syndrome, underlines the major clinical criteria of the syndrome and the major implication of B3GALTL gene in this condition.

  7. Novel B3GALTL mutation in Peters-plus Syndrome

  8. B3GTL is transcribed in a wide range of tissues and has conserved domains and motifs

  9. We report here the molecular cloning and characterization of a novel beta1,3-glucosyltransferase (beta3Glc-T) that synthesizes a Glcbeta1,3Fucalpha- structure on the TSR (zeige CFL1 ELISA Kits) domain.

  10. Biallelic truncating mutations in the beta 1,3-galactosyltransferase-like gene (B3GALTL) in all 20 tested patients, showed that Peters Plus is a monogenic, primarily single-mutation syndrome.

B3GALTL Antigen-Profil

Beschreibung des Gens

The protein encoded by this gene is a beta-1,3-glucosyltransferase that transfers glucose to O-linked fucosylglycans on thrombospondin type-1 repeats (TSRs) of several proteins. The encoded protein is a type II membrane protein. Defects in this gene are a cause of Peters-plus syndrome (PPS).

Genbezeichner und Symbole assoziert mit B3GALTL

  • beta 3-glucosyltransferase (B3GLCT) Antikörper
  • beta 3-glucosyltransferase (b3glct) Antikörper
  • beta 3-glucosyltransferase L homeolog (b3glct.L) Antikörper
  • beta-3-glucosyltransferase (B3glct) Antikörper
  • B3Glc-T Antikörper
  • B3GLCT Antikörper
  • B3GTL Antikörper
  • beta3Glc-T Antikörper
  • Gal-T Antikörper
  • Gm1057 Antikörper

Bezeichner auf Proteinebene für B3GALTL

beta 1,3-galactosyltransferase-like , beta 3-glycosyltransferase-like , UDP-GAL:beta-GlcNAc beta-1,3-galactosyltransferase-like , beta-1,3-glucosyltransferase , beta-3-glycosyltransferase-like , beta3Glc-T , beta-1,3-glucosyltransferase-like

GENE ID SPEZIES
428075 Gallus gallus
780006 Xenopus (Silurana) tropicalis
100127336 Xenopus laevis
145173 Homo sapiens
381694 Mus musculus
101111560 Ovis aries
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