N-Lactoyl-Phenylalanine是一种可由运动诱导的血源性信号代谢物,能抑制进食和肥胖,可用于肥胖研究。
分子量 | 237.25 |
分子式 | C12H15NO4 |
CAS号 | 183241-73-8 |
性状 | Solid |
溶解性 | Water 15 mg/mL |
储存条件 |
粉末型式 -20°C 3年;4°C 2年 溶于溶剂 -80°C 6个月;-20°C 1个月 |
运输方式 | 冰袋运输,根据产品的不同,可能会有相应调整。 |
N-Lactoyl-Phenylalanine是一种可由运动诱导的血源性信号代谢物,能抑制进食和肥胖,可用于肥胖研究。
General animal information(仅供参考)
Animal experiments were performed according to procedure approved by the Stanford University Administrative Panel on Laboratory Animal Care (APLAC). Studies with ABCC5-KO mice were approved by the Institute Animal Care and use Committee of the Netherlands Cancer Institute. Mice were maintained in 12-hr light-dark cycles at 22 °C and ~50% relative humidity and fed a standard irradiated rodent chow diet. Where indicated, high-fat diet (Research Diets 60% kcal from fat) was used. Male C57BL/6J and male C57BL/6J DIO mice were purchased from Jackson Laboratory. Male C57BL/6NCrl mice were purchased from Charles River Laboratory. Whole body CNDP2-KO mice were obtained from the Mutant Mouse Regional Resource Center, a NCRR-NIH funded strain repository. ABCC5-KO mice were obtained from De Wolf et al.28 For in vivo injection of mice with compounds including Lac-Phe, lactate, and phenylalanine, compounds were dissolved in 18:1:1 (by volume) of saline/Kolliphor EL/DMSO. Compounds were administered to mice daily via intraperitoneal injections at 5 μl/g body weight at the indicated doses. For all injection experiments, mice were mock injected with the vehicle for 3–5 days until body weights have stabilized. For glucose tolerance tests, mice were fasted for 6 hours then injected with glucose at 10 μl/g body weight. A dose of 1 g/kg was used for the GTT of vehicle and Lac-Phe treated obese mice. Sample sizes were determined on the basis of previous experiments using similar methodologies. For metabolite administration experiments, mice were randomly assigned to treatment groups. Experimenters were not blinded to groups.
下述溶液配置方法仅为基于分子量计算出的理论值。不同产品在配置溶液前,需考虑其在不同溶剂中的溶解度限制。
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 4.215 mL | 21.0748 mL | 42.1496 mL |
5 mM | 0.843 mL | 4.215 mL | 8.4299 mL |
10 mM | 0.4215 mL | 2.1075 mL | 4.215 mL |
*吸湿的DMSO对产品的溶解度有显著影响,请使用新开封的DMSO;
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
建议您制定动物给药及实验方案时,尽量参考已发表的相关实验文献(溶剂种类及配比众多,简单地溶解目的化合物,并不能解决动物给药依从性、体内生物利用度、组织分布等相关问题,未必能保证目的化合物在动物体内充分发挥生物学效用)。
体内实验的工作液,建议您现用现配,当天使用;如在配制过程中出现沉淀、析出现象,可以通过超声和(或)加热的方式助溶。
切勿一次性将产品全部溶解。
请在下面的计算器中,输入您的动物实验相关数据并点击计算,即可得到该实验的总需药量和工作液终浓度。
例如您给药剂量是10 mg/kg,平均每只动物的体重为20 g,每只动物的给药体积是100 μL,动物数量为20只,则该动物实验的总需药量为4 mg,工作液终浓度为2 mg/mL。
1:鉴于实验过程的损耗,建议您至少多配1-2只动物的量;
2:为该产品最终给药时的浓度。