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GlcAT-I Antibody (D-7): sc-390475

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Datasheets
  • GlcAT-I Antibody (D-7) is a mouse monoclonal IgM κ GlcAT-I antibody, cited in 3 publications, provided at 200 µg/ml
  • specific for an epitope mapping between amino acids 323-334 at the C-terminus of GlcAT-I of human origin
  • recommended for detection of GlcAT-I of mouse, rat and human origin by WB, IP, IF, IHC(P) and ELISA
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for GlcAT-I Antibody (D-7). This work is in progress.

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GlcAT-I Antibody (D-7) is a mouse monoclonal IgM antibody that detects GlcAT-I protein of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), immunohistochemistry, and enzyme-linked immunosorbent assay (ELISA). Anti-GlcAT-I antibody (D-7) is available as the non-conjugated form. GlcAT-I, also known as beta-1,3-glucuronyltransferase 3 (B3GAT3), is a 335 amino acid single-pass type II membrane protein that belongs to the glycosyltransferase 43 family. GlcAT-I plays a crucial role in proteoglycan biosynthesis by catalyzing the formation of the glycosaminoglycan-protein linkage through a glucuronyl transfer reaction, utilizing manganese as a cofactor. GlcAT-I shows strict specificity for the Gal-beta-1,3-Gal-beta-1,4-Xyl linkage, which is essential for the structural integrity and function of proteoglycans in the extracellular matrix. GlcAT-I exists as a disulfide-linked homodimer and is ubiquitously expressed, with localization primarily in the Golgi apparatus membrane, where N-glycosylation occurs to influence activity and stability.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

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GlcAT-I Antibody (D-7) References:

  1. Characterization of recombinant human glucuronyltransferase I involved in the biosynthesis of the glycosaminoglycan-protein linkage region of proteoglycans.  |  Tone, Y., et al. 1999. FEBS Lett. 459: 415-20. PMID: 10526176
  2. Structure/function of the human Ga1beta1,3-glucuronosyltransferase. Dimerization and functional activity are mediated by two crucial cysteine residues.  |  Ouzzine, M., et al. 2000. J Biol Chem. 275: 28254-60. PMID: 10842173
  3. Heparan/chondroitin sulfate biosynthesis. Structure and mechanism of human glucuronyltransferase I.  |  Pedersen, LC., et al. 2000. J Biol Chem. 275: 34580-5. PMID: 10946001
  4. The functional glycosyltransferase signature sequence of the human beta 1,3-glucuronosyltransferase is a XDD motif.  |  Gulberti, S., et al. 2003. J Biol Chem. 278: 32219-26. PMID: 12794088
  5. Phosphorylation and sulfation of oligosaccharide substrates critically influence the activity of human beta1,4-galactosyltransferase 7 (GalT-I) and beta1,3-glucuronosyltransferase I (GlcAT-I) involved in the biosynthesis of the glycosaminoglycan-protein linkage region of proteoglycans.  |  Gulberti, S., et al. 2005. J Biol Chem. 280: 1417-25. PMID: 15522873
  6. Stimulation of proteoglycan synthesis by glucuronosyltransferase-I gene delivery: a strategy to promote cartilage repair.  |  Venkatesan, N., et al. 2004. Proc Natl Acad Sci U S A. 101: 18087-92. PMID: 15601778
  7. Molecular basis for acceptor substrate specificity of the human beta1,3-glucuronosyltransferases GlcAT-I and GlcAT-P involved in glycosaminoglycan and HNK-1 carbohydrate epitope biosynthesis, respectively.  |  Fondeur-Gelinotte, M., et al. 2007. Glycobiology. 17: 857-67. PMID: 17567734
  8. 2-o-phosphorylation of xylose and 6-o-sulfation of galactose in the protein linkage region of glycosaminoglycans influence the glucuronyltransferase-I activity involved in the linkage region synthesis.  |  Tone, Y., et al. 2008. J Biol Chem. 283: 16801-7. PMID: 18400750
  9. Molecular cloning and expression of glucuronyltransferase I involved in the biosynthesis of the glycosaminoglycan-protein linkage region of proteoglycans.  |  Kitagawa, H., et al. 1998. J Biol Chem. 273: 6615-8. PMID: 9506957

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

GlcAT-I Antibody (D-7)

sc-390475
200 µg/ml
$316.00

GlcAT-I (D-7) Neutralizing Peptide

sc-390475 P
100 µg/0.5 ml
$68.00

What application is the blocking peptide sc-390475 P appropriate for?

Asked by: Trav11
Thank you for your question. The blocking peptide is intended for use as a negative control, by pre-adsorbing the mouse monoclonal antibody against the antigen. For full protocol details, please contact our Technical Services Department or view our online protocol here: https://www.scbt.com/scbt/resources/protocols/peptide-neutralization
Answered by: Technical Support
Date published: 2017-02-28
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Rated 4 out of 5 by from Clean detection of overexpressed B3GAT3Produced one clean and specific band in Western blot with HEK293 cells tranfected with B3GAT3 plasmid. No background bands.
Date published: 2021-02-11
Rated 5 out of 5 by from Excellent immunoperoxidase cytoplasmic stainingExcellent immunoperoxidase cytoplasmic staining in formalin fixed, paraffin-embedded human liver tissue. -SCBT QC
Date published: 2015-04-24
Rated 5 out of 5 by from Produced positive Western Blot data of GlcATProduced positive Western Blot data of GlcAT-I expression in CCRF-CEM, MOLT-4 and SUP-T1 whole cell lysates. -SCBT QC
Date published: 2013-02-07
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GlcAT-I Antibody (D-7) is rated 4.7 out of 5 by 3.
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