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  1. Cell Cycle/DNA Damage
  2. Nucleoside Antimetabolite/Analog
  3. 6-Mercaptopurine hydrate

6-Mercaptopurine hydrate  (Synonyms: 6-巰基嘌呤 一水合物; Mercaptopurine hydrate; 6-MP hydrate)

目錄號: HY-13677A 純度: 99.74%
COA 產(chǎn)品使用指南

6-Mercaptopurine hydrate (Mercaptopurine hydrate; 6-MP hydrate) 是一種嘌呤類似物,是內(nèi)源性嘌呤的拮抗劑且已被廣泛用作抗白血病活性分子和免疫抑制活性分子。

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6-Mercaptopurine hydrate Chemical Structure

6-Mercaptopurine hydrate Chemical Structure

CAS No. : 6112-76-1

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規(guī)格 價格 是否有貨 數(shù)量
10 mM * 1 mL in DMSO ¥258
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5 mg ¥235
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10 mg ¥330
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50 mg ¥450
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100 mg ¥650
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500 mg ¥990
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1 g   詢價  
5 g   詢價  

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Customer Review

Other Forms of 6-Mercaptopurine hydrate:

    6-Mercaptopurine hydrate purchased from MCE. Usage Cited in: Nat Commun. 2022 Nov 17;13(1):7031.  [Abstract]

    6-Mercaptopurine (6-MP; 300 μM; pretreatment for 2 h) significantly inhibits EcSTH-induced phosphorylation of AMPK and ACC1 in HeLaTet-on EcSTH and MDA-MB-231Tet-on EcSTH cells.
    • 生物活性

    • 實驗參考方法

    • 純度 & 產(chǎn)品資料

    • 參考文獻

    生物活性

    6-Mercaptopurine hydrate (Mercaptopurine hydrate; 6-MP hydrate) is a purine analogue which acts as an antagonist of the endogenous purines and has been widely used as antileukemic agent and immunosuppressive agent.

    IC50 & Target

    endogenous purines[1]

    體外研究
    (In Vitro)

    6-Mercaptopurine hydrate (Mercaptopurine hydrate;6-MP hydrate) 以劑量響應(yīng)方式誘導(dǎo) NR4A3 轉(zhuǎn)錄活性 1.6 至 11 倍 (P<0.01)。結(jié)果發(fā)現(xiàn),6-Mercaptopurine hydrate 導(dǎo)致 NR4A3 蛋白水平呈劑量依賴性增加。
    6-Mercaptopurine hydrate 處理使基底細胞和胰島素中的細胞表面 GLUT4 增加 1.8 至 3.6 倍 (P<0.01) -刺激細胞比對照組高 2.9 至 4.4 倍 (P<0.01)。還發(fā)現(xiàn) 6-Mercaptopurine hydrate 在基礎(chǔ)和胰島素刺激條件下均以劑量響應(yīng)方式顯著增加磷酸化 AS160[2]

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

    體內(nèi)研究
    (In Vivo)

    6-Mercaptopurine hydrate (6-MP) 處理組的胎兒端腦中,S 期細胞群在 36 和 48 小時增加,并在處理后 72 小時恢復(fù)到對照水平。G2/M期細胞數(shù)量在24小時開始增加,在36小時達到峰值,在48小時減少,最后在72小時回到對照水平。另一方面,亞G1期細胞群 (凋亡細胞) 在36小時開始增加,48小時達到峰值,然后在72小時減少[3]

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

    Clinical Trial
    分子量

    170.19

    Formula

    C5H6N4OS

    CAS 號
    性狀

    固體

    顏色

    Light yellow to yellow

    中文名稱

    6-巰基嘌呤水合物;6-巰基嘌呤 一水合物

    運輸條件

    Room temperature in continental US; may vary elsewhere.

    儲存方式
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 2 years
    -20°C 1 year
    溶解性數(shù)據(jù)
    細胞實驗: 

    DMSO 中的溶解度 : 50 mg/mL (293.79 mM; 超聲助溶; 吸濕的 DMSO 對產(chǎn)品的溶解度有顯著影響,請使用新開封的 DMSO)

    H2O 中的溶解度 : < 0.1 mg/mL (insoluble)

    配制儲備液
    濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg
    1 mM 5.8758 mL 29.3789 mL 58.7579 mL
    5 mM 1.1752 mL 5.8758 mL 11.7516 mL
    查看完整儲備液配制表

    * 請根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲備液;一旦配成溶液,請分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效。
    儲備液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C儲存時,請在2年內(nèi)使用, -20°C儲存時,請在1年內(nèi)使用。

    • 摩爾計算器

    • 稀釋計算器

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

    質(zhì)量
    =
    濃度
    ×
    體積
    ×
    分子量 *

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

    This equation is commonly abbreviated as: C1V1 = C2V2

    濃度 (start)

    C1

    ×
    體積 (start)

    V1

    =
    濃度 (final)

    C2

    ×
    體積 (final)

    V2

    動物實驗:

    請根據(jù)您的 實驗動物和給藥方式 選擇適當?shù)娜芙夥桨浮?

    以下溶解方案都請先按照 In Vitro 方式配制澄清的儲備液,再依次添加助溶劑:
    ——為保證實驗結(jié)果的可靠性,澄清的儲備液可以根據(jù)儲存條件,適當保存;體內(nèi)實驗的工作液,建議您現(xiàn)用現(xiàn)配,當天使用
    以下溶劑前顯示的百分比是指該溶劑在您配制終溶液中的體積占比;如在配制過程中出現(xiàn)沉淀、析出現(xiàn)象,可以通過加熱和/或超聲的方式助溶

    • 方案 一

      請依序添加每種溶劑: 10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.5 mg/mL (14.69 mM); 澄清溶液

      此方案可獲得 ≥ 2.5 mg/mL(飽和度未知)的澄清溶液。

      1 mL 工作液為例,取 100 μL 25.0 mg/mL 的澄清 DMSO 儲備液加到 400 μL PEG300 中,混合均勻;再向上述體系中加入 50 μL Tween-80,混合均勻;然后再繼續(xù)加入 450 μL 生理鹽水 定容至 1 mL。

      生理鹽水的配制:將 0.9 g 氯化鈉,溶解于 ddH?O 并定容至 100 mL,可以得到澄清透明的生理鹽水溶液。
    動物溶解方案計算器
    請輸入動物實驗的基本信息:

    給藥劑量

    mg/kg

    動物的平均體重

    g

    每只動物的給藥體積

    μL

    動物數(shù)量

    由于實驗過程有損耗,建議您多配一只動物的量
    請輸入您的動物體內(nèi)配方組成:
    %
    DMSO +
    +
    %
    Tween-80 +
    %
    Saline
    如果您的動物是免疫缺陷鼠或者體弱鼠,建議 DMSO 中的在最后工作液體系中的占比盡量不超過 2%。
    方案所需 助溶劑 包括:DMSO, ,均可在 MCE 網(wǎng)站選購。 ,Tween 80,均可在 MCE 網(wǎng)站選購。
    計算結(jié)果
    工作液所需濃度 : mg/mL
    儲備液配制方法 : mg 藥物溶于 μL  DMSO(母液濃度為 mg/mL)。
    您所需的儲備液濃度超過該產(chǎn)品的實測溶解度,以下方案僅供參考,如有需要,請與 MCE 中國技術(shù)支持聯(lián)系。
    動物實驗體內(nèi)工作液的配制方法 : 取 μL DMSO 儲備液,加入 μL 。 μL ,混合均勻至澄清,再加 μL Tween 80,混合均勻至澄清,再加 μL 生理鹽水。
    連續(xù)給藥周期超過半月以上,請謹慎選擇該方案。
    請確保第一步儲備液溶解至澄清狀態(tài),從左到右依次添加助溶劑。您可采用超聲加熱 (超聲清洗儀,建議頻次 20-40 kHz),渦旋吹打等方式輔助溶解。
    純度 & 產(chǎn)品資料

    純度: 99.74%

    參考文獻
    Kinase Assay
    [2]

    L6 myotubes are treated with DMSO control or 6-Mercaptopurine hydrate (6-MP) for 24 h, with the final 3 h of incubation including treatments in serum-free DMEM, and further incubated in the absence or presence of 100 nM insulin for 60 min at 37°C. Then, protein lysates (50 μg) are collected and subjected to SDS-PAGE. The proteins are finally quantified by densitometric analysis of scanned films using Image J software[2].

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

    Cell Assay
    [2]

    Cell viability is measured using Cell Viability Assay. L6 skeletal muscle cells are seeded in 96-well plates at a density of 10,000 cells/well and differentiated into myotubes within 7 days. Cells are treated with different doses of 6-Mercaptopurine hydrate (6-MP) for 24 h before the assay. For analysis of cell viability, plates are equilibrated at room temperature for 30 min; 50 μL of Cell Titer-Glo reagent is added to each well, and plates are mixed for 12 min on an orbital shaker. Luminescence is quantified using a luminometer[2].

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

    Animal Administration
    [3]

    Around thirteen-week-old pregnant rats are used in this study. The animals are housed individually in wire-mesh cages in an air-conditioned room (temperature, 23±3°C; humidity, 50±20%; ventilation, 10 times/hour; lighting, 12 h light to12 h dark cycle) and are given pelleted diet and water ad libitum. In the experiment, fifteen pregnant rats are injected i.p. with 50 mg/kg 6-Mercaptopurine hydrate (6-MP) on E13, and three dams each are sacrificed by exsanguination from the abdominal aorta under ether anesthesia at 12, 24, 36, 48, and 72 h. Fetuses are collected from each dam by Caesarean section. As controls, fifteen pregnant rats are injected i.p. with 2.0% methylcellulose solution in distilled water at E13, and three dams are sacrificed at each of the same time-points[3].

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

    參考文獻

    完整儲備液配制表

    * 請根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲備液;一旦配成溶液,請分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效。
    儲備液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C儲存時,請在2年內(nèi)使用, -20°C儲存時,請在1年內(nèi)使用。

    可選溶劑 濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg 25 mg
    DMSO 1 mM 5.8758 mL 29.3789 mL 58.7579 mL 146.8946 mL
    5 mM 1.1752 mL 5.8758 mL 11.7516 mL 29.3789 mL
    10 mM 0.5876 mL 2.9379 mL 5.8758 mL 14.6895 mL
    15 mM 0.3917 mL 1.9586 mL 3.9172 mL 9.7930 mL
    20 mM 0.2938 mL 1.4689 mL 2.9379 mL 7.3447 mL
    25 mM 0.2350 mL 1.1752 mL 2.3503 mL 5.8758 mL
    30 mM 0.1959 mL 0.9793 mL 1.9586 mL 4.8965 mL
    40 mM 0.1469 mL 0.7345 mL 1.4689 mL 3.6724 mL
    50 mM 0.1175 mL 0.5876 mL 1.1752 mL 2.9379 mL
    60 mM 0.0979 mL 0.4896 mL 0.9793 mL 2.4482 mL
    80 mM 0.0734 mL 0.3672 mL 0.7345 mL 1.8362 mL
    100 mM 0.0588 mL 0.2938 mL 0.5876 mL 1.4689 mL
    Help & FAQs
    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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    產(chǎn)品名稱:
    6-Mercaptopurine hydrate
    目錄號:
    HY-13677A
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