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1373715-00-4

1373715-00-4 structure
1373715-00-4 structure
  • Name: Luspatercept
  • Chemical Name: Luspatercept
  • CAS Number: 1373715-00-4
  • Molecular Formula:
  • Molecular Weight:
  • Catalog: Signaling Pathways Stem Cell/Wnt TGF-beta/Smad
  • Create Date: 2018-07-18 12:17:14
  • Modify Date: 2024-01-11 19:33:09
  • Luspatercept (ACE-536) is a recombinant modified ActRIIB fusion protein that binds with transforming growth factor β superfamily ligands. Luspatercept increases the erythrocyte numbers and promotes maturation of erythroid precursors. Luspatercept binds with GDF11 and inhibits Smad2/3 signaling. Luspatercept can be used for the research of anemia[1].

Name Luspatercept
Description Luspatercept (ACE-536) is a recombinant modified ActRIIB fusion protein that binds with transforming growth factor β superfamily ligands. Luspatercept increases the erythrocyte numbers and promotes maturation of erythroid precursors. Luspatercept binds with GDF11 and inhibits Smad2/3 signaling. Luspatercept can be used for the research of anemia[1].
Related Catalog
In Vitro Luspatercept (0.1-1000 ng/mL) 抑制 A204 细胞中 GDF11 和 GDF8 诱导的 Smad2 和 Smad 3 信号通路[1]。 Luspatcept 与 GDF11,GDF8,activin B,BMP10 和 BMP6 结合[1]。
In Vivo Luspatercept (0.1-60mg /kg,皮下注射;10mg /kg,静脉注射;每周 2 次,共 8 周) 增加小鼠、大鼠和猴子的红细胞 (RBC) 数量、血红蛋白水平和红细胞堆积[1]。 Luspatercept (10mg /kg,皮下注射,1 次) 降低 C57BL/6 小鼠骨髓和脾脏中的红细胞形成单位 (BFU-Es) 和红血球形成单位 (CFU-Es)[1]。 Luspatercept (10mg /kg,腹腔注射,1 次) 抑制小鼠脾脏 Smad2/3 磷酸化[1]。 Animal Model: C57BL/6 mice[1] Dosage: 0.1, 0.3, 1, 3 and 10 mg/kg Administration: Subcutaneous injection and intravenous injection; 0.1-10 mg/kg (C57BL/6 mice, s.c.), 6-60 mg/kg (Sprague Dawley rats, s.c.), 0.4-30 mg/kg (cynomolgus monkeys, s.c.), 10 mg/kg, (cynomolgus monkeys, i.v.); twice weekly for 8 weeks Result: Dose-dependently increased the level of RBC, hemoglobin and hematocrit in mice, rats and monkeys.
References

[1]. Suragani RN, et al. Transforming growth factor-β superfamily ligand trap ACE-536 corrects anemia by promoting late-stage erythropoiesis. Nat Med. 2014 Apr;20(4):408-14.  

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