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Teriparatide

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产品编号 T13128Cas号 52232-67-4
别名 特立帕肽, PTH 1-34, Human parathyroid hormone-(1-34), hPTH (1-34)

Teriparatide is an agonist of PHT(IC50 of 2 nM in HEK293 cells).

Teriparatide

Teriparatide

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产品编号 T13128 别名 特立帕肽, PTH 1-34, Human parathyroid hormone-(1-34), hPTH (1-34)Cas号 52232-67-4

Teriparatide is an agonist of PHT(IC50 of 2 nM in HEK293 cells).

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产品介绍

生物活性
产品描述
Teriparatide is an agonist of PHT(IC50 of 2 nM in HEK293 cells).
靶点活性
PTH:2 nM
体内活性
In Teriparatide-treated animals, Trabecular bone calcium and dry weight of the distal femur increased significantly. The increase in trabecular calcium compared with vehicle control occurred as early as 1 week after initiation of treatment with a 35% and 45% increase, respectively, for 10 μg/kg and 40 μg/kg Teriparatide. Similar results were observed for trabecular dry weight. After 4 weeks of treatment with 10 mg/kg or 40 mg/kg Teriparatide, trabecular calcium increased significantly by 70% and 123%, respectively, compared with the vehicle and by 73%. The 4-week Teriparatide administration + 8-week vehicle administration decrease the pore ratio, number, and density as well as the cortical area and thickness, compared with the 4-week Teriparatide administration, but the pore ratio, cortical area, and thickness are still higher compared with the 12-week vehicle administration. The 4-week Teriparatide administration increase the pore ratio, number, and density as well as the cortical area, thickness, and bone mineral content (BMC), without significant influencing the volumetric bone mineral density (BMD). The 4-week Teriparatide administration + 8-week higherdose IBN administration increase the cortical area, thickness, BMC, and volumetric BMD and decrease the pore ratio, but not the pore number or density, compared with the 4-week Teriparatide administration + 8-week vehicle administration.
别名特立帕肽, PTH 1-34, Human parathyroid hormone-(1-34), hPTH (1-34)
化学信息
分子量4117.72
分子式C181H291N55O51S2
CAS No.52232-67-4
密度no data available
储存&溶解度
存储keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度信息
H2O: 50 mg/mL (12.14 mM)
溶液配制表
H2O
1mg5mg10mg50mg
1 mM0.2429 mL1.2143 mL2.4285 mL12.1426 mL
5 mM0.0486 mL0.2429 mL0.4857 mL2.4285 mL
10 mM0.0243 mL0.1214 mL0.2429 mL1.2143 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments比如您的给药剂量是 10 mg/kg ,每只动物体重 20 g ,给药体积 100 μLTargetMol | Animal experiments 一共给药动物 10 只 ,您使用的配方为 5% TargetMol | reagent DMSO+ 30%PEG300+ 5%Tween 80 + 60% ddH2O. 那么您的工作液浓度为 2 mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween 80, 混匀澄清,再加 600μLddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
%Tween 80
%ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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