Name: N-Acetyl-D-lactosamine
Price: Inquiry

- Overview
  - Please contact us at for specific academic pricing.
- Properties
  - Categories
    
    Lactooligosaccharides
    
    Alternative Name
    
    LacNAc;Galactopyranosyl-b-1,4-N-acetyl-D-glucosamine;2-Acetamido-2-deoxy-D-lactose;Galb1-4GlcNAc
    
    CAS Number
    
    32181-59-2
    
    Molecular Formula
    
    C14H25NO11
    
    Molecular Weight
    
    383.35 g/mol
    
    MDL Number
    
    MFCD00063785
    
    Note
    
    There is no hazardous surcharge associated with this product.
    There is no special packaging charge associated with this product.
    
    * For research use only. Not for human or veterinary use
- Reference
  - Gunnarsson et al (1984). Oligosaccharide structures mediating agglutination of sheep erythrocytes by Staphylococcus saprophyticus. Infection and Immunity. 45(1):41-6.
    Zhou (2003). Why are glycoproteins modified by poly-N-acetyllactosamine glyco-conjugates. Current Protein and Peptide Science. 4(1): 1–9.
    Loomes et al (1984). Erythrocyte receptors for Mycoplasma pneumoniae are sialylated oligosaccharides of Ii antigen type. Nature 307: 560.
    Ito et al (1996) Histochemical demonstration and analysis of poly-N-acetyllactosamine structures in normal and malignant human tissues. Histolgy and Histopathology. 11(1): 203–14.
    Prieels et al (1981). Co-purification of the Lewis blood group N-acetylglucosaminide alpha 1 goes to 4 fucosyltransferase and an N-acetylglucosaminide alpha 1 goes to 3 fucosyltransferase from human milk. Journal of Biological Chemistry. 256: 10456.
    Shinohara et al (1996). Bifunctional labeling reagent for oligosaccharides to incorporate both chromophore and biotin groups. Analytical Chemistry. 68: 2573-2579.
    Drechsler et al (2015). Galectin-3, Renal Function, and Clinical Outcomes: Results from the LURIC and 4D Studies. Journal of the American Society of Nephrology. 26: 2213-2221.