Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Maltotetraose (Fujioligo 450) are potent inhibitors of TNF-α-induced intercellular adhesion molecule-1 (ICAM-1) expression, maltotetraose may be beneficial in the suppression of early atherosclerosis development.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
5 mg | In stock | $ 42.00 | |
10 mg | In stock | $ 66.00 | |
25 mg | In stock | $ 97.00 | |
50 mg | In stock | $ 158.00 |
Description | Maltotetraose (Fujioligo 450) are potent inhibitors of TNF-α-induced intercellular adhesion molecule-1 (ICAM-1) expression, maltotetraose may be beneficial in the suppression of early atherosclerosis development. |
In vivo | Maltotetraose reduced PDGF-induced sprout formation by mouse aorta explants and inhibited TNF-α-induced NF-κB activation and ICAM-1 expression in MOVAS-1 cells[1]. |
Animal Research | Ex vivo migration of VSMCs was measured by aortic . Mouse thoracic aortas were excised from 8-week-old male Balb/c mice and adipose tissue was removed. The aortas were sectioned into 1-mm–long cross-sections, rinsed with serum-free DMEM, treated with 1 mg/mL collagenenase type II, placed in matrigel-coated wells, covered with 50 uL matrigel, and allowed to gel for more than 30 min at 37℃ in a 5% CO2 atmosphere. The aortic rings were treated with 20 ug/mL MALTOTETRAOSE for 30 min, followed by stimulation with 20 ng/mL PDGF-BB. Aortic ring sprouts were photographed on day 7[1]. |
Synonyms | Fujioligo 450, Amylotetraose, α-1,4-Tetraglucose |
Molecular Weight | 666.58 |
Formula | C24H42O21 |
CAS No. | 34612-38-9 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 55 mg/mL (82.51 mM)
You can also refer to dose conversion for different animals. More
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MALTOTETRAOSE 34612-38-9 Apoptosis Metabolism TNF Endogenous Metabolite Fujioligo-450 Inhibitor Fujioligo 450 inhibit Amylotetraose a-1,4-Tetraglucose α-1,4-Tetraglucose Fujioligo450 alpha-1,4-Tetraglucose inhibitor