1. Cell Cycle/DNA Damage
    Cytoskeleton
    Antibody-drug Conjugate/ADC Related
    Apoptosis
    Autophagy
  2. Microtubule/Tubulin
    ADC Cytotoxin
    Apoptosis
    Autophagy
  3. Paclitaxel

Paclitaxel (Synonyms: 紫杉醇)

目录号: HY-B0015 纯度: 99.96%
产品使用指南

Paclitaxel 是一种天然抗肿瘤药,可稳定微管蛋白 (tubulin) 的聚合。Paclitaxel 可导致有丝分裂停滞和诱导细胞凋亡 (apoptosis),最终导致细胞死亡。Paclitaxel 还可诱导细胞自噬 (autophagy)。

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Paclitaxel Chemical Structure <

Paclitaxel Chemical Structure

CAS No. : 33069-62-4

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10 mM * 1 mL in DMSO ¥572
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10 mg ¥520
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50 mg ¥900
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100 mg ¥1500
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500 mg ¥5000
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Top Publications Citing Use of Products

MCE 顾客使用本产品发表的 102 篇科研文献

    Paclitaxel purchased from MCE. Usage Cited in: Am J Cancer Res. 2017 Apr 1;7(4):903-912.

    Synergistic inhibition of colony formation of ATC cells by E7080 and Paclitaxel. Representative images of colony formation in C643 cells treated with vehicle control (DMSO) or E7080 and Paclitaxel at the indicated concentrations, individually or in combination, are shown in left panel. Quantitative analysis of colony numbers is shown in right panel.

    Paclitaxel purchased from MCE. Usage Cited in: Biochim Biophys Acta. 2018 May;1862(5):1134-1147.

    The effects of CS1 on polymerized microtubules are also investigated using a cellular tubulin polymer assay. Nocodazole (1 μM) and Paclitaxel (1.5 μM) are used as depolymerization and polymerization controls, respectively.

    Paclitaxel purchased from MCE. Usage Cited in: J Agric Food Chem. 2019 Feb 13;67(6):1656-1665.

    Western blot image and statistical analysis of phosphorylated γH2AX levels in HT-29 cells with different treatments after 48 h. Myricetin and PTX used are 32 μM and 100 nM, respectively.
    • 生物活性

    • 纯度 & 产品资料

    • 参考文献

    生物活性

    Paclitaxel is a naturally occurring antineoplastic agent and stabilizes tubulin polymerization. Paclitaxel can cause both mitotic arrest and apoptotic cell death. Paclitaxel also induces autophagy[1][2].

    IC50 & Target[1]

    Traditional Cytotoxic Agents

     

    体外研究
    (In Vitro)

    Paclitaxel (20 nM; 48 hours) induces programmed cell death and exists a block at the G2/M phase of the cell cycle[1].
    Paclitaxel (20 nM; 48 hours) induces a consistent increase in the level of p53[1].

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

    Apoptosis Analysis[1]

    Cell Line: MCF-7, MDA-MB-231 cells
    Concentration: 20 nM
    Incubation Time: 48 hours
    Result: Induced programmed cell death.

    Cell Cycle Analysis[1]

    Cell Line: MCF-7, MDA-MB-231 cells
    Concentration: 20 nM
    Incubation Time: 48 hours
    Result: >60% of MCF-7 cells and 50% of MDA-MB-231 cells were in the G2/M phase following 24 h treament.

    Western Blot Analysis[1]

    Cell Line: MCF-7 cells (harboring wild-type p53)
    Concentration: 20 nM
    Incubation Time: 48 hours
    Result: Induced a consistent increase in the level of p53.
    体内研究
    (In Vivo)

    Paclitaxel (1-20 mg/kg; i.p.; 1 time/2 days for five cycles) obviously induces liver metastases at the low-Paclitaxel group with little influence on primary tumor growth[3].

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

    Animal Model: MDA-231 xenograft-bearing mice[3]
    Dosage: 1, 20 mg/kg
    Administration: Intraperitoneal injection; five cycles (1 time/2 days)
    Result: Liver metastases were obviously induced in the low-PTX (1 mg/kg) group with little influence on primary tumor growth compared with high-PTX group.
    Clinical Trial
    分子量

    853.91

    Formula

    C47H51NO14

    CAS 号
    中文名称

    紫杉醇

    结构分类
    来源
    运输条件

    Room temperature in continental US; may vary elsewhere.

    储存方式

    4°C, protect from light

    *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

    溶解性数据
    In Vitro: 

    DMSO : 100 mg/mL (117.11 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 1.1711 mL 5.8554 mL 11.7108 mL
    5 mM 0.2342 mL 1.1711 mL 2.3422 mL
    10 mM 0.1171 mL 0.5855 mL 1.1711 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 (protect from light)。-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 (2.44 mM); Clear solution

      此方案可获得 ≥ 2.08 mg/mL (2.44 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 (2.44 mM); Suspended solution; Need ultrasonic

      此方案可获得 2.08 mg/mL (2.44 mM) 的均匀悬浊液,悬浊液可用于口服和腹腔注射。

      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 (2.44 mM); Clear solution

      此方案可获得 ≥ 2.08 mg/mL (2.44 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 MCE 网站选购。
    参考文献

    纯度: 99.97%

    • 摩尔计算器

    • 稀释计算器

    The molarity calculator equation

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

    质量   浓度   体积   分子量 *
    = × ×

    The dilution calculator equation

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
    × = ×
    C1   V1   C2   V2

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    目录号:
    HY-B0015
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