Date published: 2025-10-20

1-800-457-3801

SCBT Portrait Logo
Seach Input

3α,4β,3α-Galactotetraose (CAS 56038-38-1)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Galalpha1-3Galbeta1-4Galalpha1-3Gal
Application:
3α,4β,3α-Galactotetraose is a short polymer with 4 galactose monomers
CAS Number:
56038-38-1
Purity:
≥95%
Molecular Weight:
666.58
Molecular Formula:
C24H42O21
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

3α,4β,3α-Galactotetraose is a complex oligosaccharide that plays a pivotal role in glycobiology research, especially in studies related to carbohydrate-based interactions in biological systems. This tetrasaccharide, consisting of galactose units linked by specific glycosidic bonds, serves as an essential tool for investigating the specificity and mechanism of glycosidases and glycosyltransferases—enzymes critical for the synthesis and breakdown of glycan structures. Its unique structure enables the study of carbohydrate recognition by lectins, which are proteins that bind sugar molecules and mediate cellular interactions and signaling pathways. Research utilizing 3α,4β,3α-Galactotetraose often focuses on elucidating how these sugar molecules influence cellular recognition processes, such as cell adhesion, immune response modulation, and pathogen invasion. Furthermore, this oligosaccharide is used in the development of synthetic glycans that mimic natural structures, aiding in the exploration of their biological functions and their potential role in modulating biological processes. The insights gained from these studies contribute significantly to the understanding of glycoscience, particularly in how sugars affect complex biological systems and their potential to influence biochemical pathways.


3α,4β,3α-Galactotetraose (CAS 56038-38-1) References

  1. MALDI linear-field reflectron TOF post-source decay analysis of underivatized oligosaccharides: determination of glycosidic linkages and anomeric configurations using anion attachment.  |  Guan, B. and Cole, RB. 2008. J Am Soc Mass Spectrom. 19: 1119-31. PMID: 18554925
  2. Fed-batch synthesis of galacto-oligosaccharides with Aspergillus oryzae β-galactosidase using optimal control strategy.  |  Vera, C., et al. 2014. Biotechnol Prog. 30: 59-67. PMID: 24167086
  3. Production of galactooligosaccharides using a hyperthermophilic β-galactosidase in permeabilized whole cells of Lactococcus lactis.  |  Yu, L. and O'Sullivan, DJ. 2014. J Dairy Sci. 97: 694-703. PMID: 24359820
  4. Alteration and localization of glycan-binding proteins in human hepatic stellate cells during liver fibrosis.  |  Zhong, Y., et al. 2015. Proteomics. 15: 3283-95. PMID: 26058380
  5. Electron Transfer Dissociation and Collision-Induced Dissociation of Underivatized Metallated Oligosaccharides.  |  Schaller-Duke, RM., et al. 2018. J Am Soc Mass Spectrom. 29: 1021-1035. PMID: 29492773
  6. Creating a Mass Spectral Reference Library for Oligosaccharides in Human Milk.  |  Remoroza, CA., et al. 2018. Anal Chem. 90: 8977-8988. PMID: 29969231
  7. Ligand-aided 1H Nuclear Magnetic Resonance Spectroscopy for Non-destructive Estimation of Sulfate Content in Sulfated Saccharides.  |  Bak, J., et al. 2020. Anal Sci. 36: 1269-1273. PMID: 32565527
  8. Influence of reaction conditions on the selectivity of the synthesis of lactulose with microbial β-galactosidases.  |  Guerrero, Cecilia, et al. 2011. Journal of Molecular Catalysis B: Enzymatic. 72.3-4: 206-212.
  9. Heterologous expression of a newly screened β-agarase from Alteromonas sp. GNUM1 in Escherichia coli and its application for agarose degradation.  |  Seo, Young Bin, et al. 2014. Process Biochemistry. 49.3: 430-436.
  10. Selective bioconversion with yeast for the purification of raw lactulose and transgalactosylated oligosaccharides.  |  Guerrero, Cecilia, et al. 2018. International dairy journal. 81: 131-137.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3α,4β,3α-Galactotetraose, 2 mg

sc-256601
2 mg
$113.00