Tunicamycin

CAT:
400-SIH-397-5MG
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Tunicamycin - image 1
Tunicamycin - image 2
Thumbnail 1
Thumbnail 2

Tunicamycin

  • Background :

    As a nucleoside antibiotic, Tunicamycin blocks the formation of protein N-glycosidic linkages by inhibiting the transfer of N-acetylglucosamine 1-phosphate to dolichol monophosphate. This causes an induction of glucose-regulated protein 78 (GRP78) mRNA expression, which in turn increases ER stress and subsequently induces autophagy (1-4). Triggers a-synuclein oligomerization, dopaminergic neurons death and locomotor impariement, potentially a model for Parkinson's Disease (5).
  • Description :

    Autophagy inducer
  • Product Name Alternative :

    Tunicamycin from Streptomyces sp.
  • UNSPSC :

    41116105
  • Type :

    Inducer
  • Source :

    Isolated from Streptomyces lysosuperficus
  • Field of Research :

    Cancer | Autophagy | Neuroscience | Neurodegeneration | Parkinson's Disease | Synuclein
  • Purity :

    >98% (HPLC) as a mixture of tunicamycin A, B, C and D
  • Weight :

    0.005
  • Format :

    White solid.
  • Solubility :

    Soluble in DMSO (>10 mg/ml) or ethanol (5 mg/ml; warm).
  • Molecular Formula :

    C39H64N4O16
  • Molecular Weight :

    844.95
  • Precautions :

    Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.
  • References & Citations :

    1. Unal E.S., et al. (2008) Biochim Biophys Acta. 1778(6): 1407-14. 2. Ding W.X., et al. (2007) J Biol Chem. 282(7): 4702-10. 3. Ishii S., et al. (1987) J Neurochem. 49(5): 1606-12. 4. Zhang J., et al. (2013) J Surg Res. 183(2): 929-35. 5. Coppola-Segovia V., et al. (2016) Molecular Neuro. 54, 5798-5806.
  • CAS Number :

    11089-65-9

Featured Selection

Popular Products

Discover our most sought-after biotechnology products, trusted by researchers worldwide