Radioprotectin-1,99.51%

产品编号:Bellancom-114380| CAS NO:1622006-09-0| 分子式:C23H19ClN2O6S| 分子量:486.92

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货号 包装 价格 库存与货期 购买量 操作
Bellancom-114380
4500.00 杭州 北京(现货)
Bellancom-114380
7500.00 杭州 北京(现货)
Bellancom-114380
22000.00 杭州 北京(现货)
Bellancom-114380
33000.00 杭州 北京(现货)

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Radioprotectin-1

产品介绍 Radioprotectin-1 是一种高效特异性的溶血磷脂酸受体 2 (LPA2) 激动剂,EC50 值为 25 nM (鼠源 LPA2 亚型) 。
生物活性

Radioprotectin-1 is a potent and specific nonlipid agonist of lysophosphatidic acid receptor 2 (LPA2), with an EC50 value of 25 nM for murine LPA2 subtype.

体外研究

Radioprotectin-1 is a potent agonist of LPA2 with an EC50 of 5 pM and functions as a full agonist at the human ortholog of LPA2.
Radioprotectin-1 (0-3 μM; 15 minutes) effectively reduces apoptosis induced by γ-irradiation and the radiomimetic drug Adriamycin in cells that expressed LPA2 either endogenously or after transfection.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay

Cell Line: MEF cells , IEC-6 cells
Concentration: 0 μM, 0.1 μM, 0.3 μM, 1.0 μM,3 μM
Incubation Time: 15 minutes
Result: Protected cells from apoptosis by γ-irradiation- and the radiomimetic chemotherapeutic Adiamycin.
体内研究
(In Vivo)

Radioprotectin-1 is a high-potency specific agonist of the murine LPA2 GPCR .
Radioprotectin-1 (0.1 mg/kg, 0.3 mg/kg; s.c.; every 12 hours; for 3 days) decreases the mortality of C57BL/6 mice in models of the hematopoietic acute radiation syndromes (HE-ARS) and gastrointestinal acute radiation syndromes (GI-ARS) .
Radioprotectin-1 exerts its radioprotective and radiomitigative action through specific activation of the upregulated LPA2 GPCR in Lgr5+stem cells.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 8-10 weeks old C57BL/6 female mice bearing total body irradiation (TBI)
Dosage: 0.1 mg/kg, 0.3 mg/kg
Administration: Subcutaneous injection; every 12 hours; for 3 days
Result: Decreased mortality of C57BL/6 mice in models of the HE-ARS and the GI-ARS.
体内研究

Radioprotectin-1 is a high-potency specific agonist of the murine LPA2 GPCR .
Radioprotectin-1 (0.1 mg/kg, 0.3 mg/kg; s.c.; every 12 hours; for 3 days) decreases the mortality of C57BL/6 mice in models of the hematopoietic acute radiation syndromes (HE-ARS) and gastrointestinal acute radiation syndromes (GI-ARS) .
Radioprotectin-1 exerts its radioprotective and radiomitigative action through specific activation of the upregulated LPA2 GPCR in Lgr5+stem cells.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 8-10 weeks old C57BL/6 female mice bearing total body irradiation (TBI)
Dosage: 0.1 mg/kg, 0.3 mg/kg
Administration: Subcutaneous injection; every 12 hours; for 3 days
Result: Decreased mortality of C57BL/6 mice in models of the HE-ARS and the GI-ARS.
体内研究

Radioprotectin-1 is a high-potency specific agonist of the murine LPA2 GPCR .
Radioprotectin-1 (0.1 mg/kg, 0.3 mg/kg; s.c.; every 12 hours; for 3 days) decreases the mortality of C57BL/6 mice in models of the hematopoietic acute radiation syndromes (HE-ARS) and gastrointestinal acute radiation syndromes (GI-ARS) .
Radioprotectin-1 exerts its radioprotective and radiomitigative action through specific activation of the upregulated LPA2 GPCR in Lgr5+stem cells.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 8-10 weeks old C57BL/6 female mice bearing total body irradiation (TBI)
Dosage: 0.1 mg/kg, 0.3 mg/kg
Administration: Subcutaneous injection; every 12 hours; for 3 days
Result: Decreased mortality of C57BL/6 mice in models of the HE-ARS and the GI-ARS.
性状Solid
溶解性数据
In Vitro: 

DMSO : 125 mg/mL (256.72 mM; Need ultrasonic)

H2O : < 0.1 mg/mL (insoluble)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.0537 mL 10.2686 mL 20.5373 mL
5 mM 0.4107 mL 2.0537 mL 4.1075 mL
10 mM 0.2054 mL 1.0269 mL 2.0537 mL
*

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
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 2.08 mg/mL (4.27 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (4.27 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH₂O 中,得到澄清透明的生理盐水溶液
  • 2.

    请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.08 mg/mL (4.27 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (4.27 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 3.

    请依序添加每种溶剂: 10% DMSO    90% corn oil

    Solubility: ≥ 2.08 mg/mL (4.27 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (4.27 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在 西域 网站选购。
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献

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