Tunicamycin from Streptomyces sp.

98%

  • Product Code: 110883
  CAS:    11089-65-9
Molecular Weight: 816.89 g./mol Molecular Formula: C₃₇H₆₀N₄O₁₆
EC Number: MDL Number: MFCD00065709
Melting Point: Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Tunicamycin is widely used in biochemical research as a potent inhibitor of N-linked glycosylation. It effectively blocks the first step in the biosynthesis of N-linked glycoproteins, making it a valuable tool for studying the role of glycosylation in cellular processes, protein folding, and secretion. Researchers utilize it to investigate the effects of glycosylation on protein function, cell signaling, and the development of diseases such as cancer and viral infections. Additionally, tunicamycin is employed in studies related to endoplasmic reticulum (ER) stress and the unfolded protein response (UPR), as it induces ER stress by disrupting protein glycosylation. Its application extends to exploring potential therapeutic strategies targeting glycosylation pathways in various pathological conditions.
Product Specification:
Test Specification
Purity (HPLC) 98-100
Appearance White To Off-White To Light Yellow Crystals Or Powder
Solubility In Methanol Almost Transparency
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.001 10-20 days ฿3,990.00
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-
0.005 10-20 days ฿15,490.00
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-
Tunicamycin from Streptomyces sp.
Tunicamycin is widely used in biochemical research as a potent inhibitor of N-linked glycosylation. It effectively blocks the first step in the biosynthesis of N-linked glycoproteins, making it a valuable tool for studying the role of glycosylation in cellular processes, protein folding, and secretion. Researchers utilize it to investigate the effects of glycosylation on protein function, cell signaling, and the development of diseases such as cancer and viral infections. Additionally, tunicamycin is employed in studies related to endoplasmic reticulum (ER) stress and the unfolded protein response (UPR), as it induces ER stress by disrupting protein glycosylation. Its application extends to exploring potential therapeutic strategies targeting glycosylation pathways in various pathological conditions.
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