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  1. Immunology/Inflammation Apoptosis Anti-infection
  2. COX Apoptosis Parasite
  3. Ibuprofen

Ibuprofen  (Synonyms: 布洛芬; (±)-Ibuprofen)

目錄號: HY-78131 純度: 99.97%
COA 產(chǎn)品使用指南

Ibuprofen ((±)-Ibuprofen) 是一種口服有效的 COX-1 選擇性抑制劑,IC50 值為 13 μM。Ibuprofen 抑制細胞增殖、血管生成,并誘導(dǎo)細胞凋亡 (apoptosis)。Ibuprofen 是一種非甾體抗炎試劑和一氧化氮 (NO) 供體。Ibuprofen可用于疼痛、腫脹、炎癥、感染、免疫學(xué)、癌癥的研究。

MCE 的所有產(chǎn)品僅用作科學(xué)研究或藥證申報,我們不為任何個人用途提供產(chǎn)品和服務(wù)

Ibuprofen Chemical Structure

Ibuprofen Chemical Structure

CAS No. : 15687-27-1

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10 mM * 1 mL in DMSO ¥500
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Customer Review

Other Forms of Ibuprofen:

  • 生物活性

  • 純度 & 產(chǎn)品資料

  • 參考文獻

生物活性

Ibuprofen ((±)-Ibuprofen) is a potent, orally active, selective COX-1 inhibitor with an IC50 value of 13 μM. Ibuprofen inhibits cell proliferation, angiogenesis, and induces cell apoptosis. Ibuprofen is a nonsteroidal anti-inflammatory agent and a nitric oxide (NO) donor. Ibuprofen ((±)-Ibuprofen) can be used in the research of pain, swelling, inflammation, infection, immunology, cancers[1][2][5][8].

IC50 & Target[1]

COX-1

13 μM (IC50)

COX-2

370 μM (IC50)

細胞效力
(Cellular Effect)
Cell Line Type Value Description References
Bel-7402 IC50
> 100 μM
Compound: Ibuprofen
Antiproliferative activity against human Bel7402 cells after 72 hrs by CCK-8 assay
Antiproliferative activity against human Bel7402 cells after 72 hrs by CCK-8 assay
[PMID: 28301815]
Bel7402/5-FU IC50
> 100 μM
Compound: Ibuprofen
Antiproliferative activity against human Bel7402/5-FU cells after 72 hrs by CCK-8 assay
Antiproliferative activity against human Bel7402/5-FU cells after 72 hrs by CCK-8 assay
[PMID: 28301815]
BGC-823 IC50
> 50 μM
Compound: Ibuprofen
Cytotoxicity against human BGC-823 cells assessed as reduction in cell viability measured upto 72 hrs by MTT assay
Cytotoxicity against human BGC-823 cells assessed as reduction in cell viability measured upto 72 hrs by MTT assay
[PMID: 33799070]
Caco-2 IC50
> 50 μM
Compound: Ibuprofen
Cytotoxicity against human Caco2 cells assessed as reduction in cell viability measured upto 72 hrs by MTT assay
Cytotoxicity against human Caco2 cells assessed as reduction in cell viability measured upto 72 hrs by MTT assay
[PMID: 33799070]
CHO IC50
200 μM
Compound: 1
Modulation of gamma-secretase-mediated cleavage of human APP expressed in CHO cells with human presenilin-1 assessed as inhibition of amyloid beta42 production after 24 hrs by ELISA
Modulation of gamma-secretase-mediated cleavage of human APP expressed in CHO cells with human presenilin-1 assessed as inhibition of amyloid beta42 production after 24 hrs by ELISA
[PMID: 20503989]
CHO IC50
200 μM
Compound: 1
Modulation of gamma-secretase expressed in CHO cells co-expressing human APP and wild type human presenilin-1 assessed as inhibition of amyloid beta42 production by ELISA
Modulation of gamma-secretase expressed in CHO cells co-expressing human APP and wild type human presenilin-1 assessed as inhibition of amyloid beta42 production by ELISA
[PMID: 21873070]
COS-7 IC50
> 1000 μM
Compound: Ibuprofen
Cytotoxicity against African green monkey COS7 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
Cytotoxicity against African green monkey COS7 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
[PMID: 32527536]
HCT-116 IC50
448 μM
Compound: IB
Cytotoxicity against human HCT116 cells after 72 hrs by MTT assay
Cytotoxicity against human HCT116 cells after 72 hrs by MTT assay
[PMID: 20171760]
HCT-15 IC50
> 1000 μM
Compound: Ibuprofen
Anticancer activity against human HCT15 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
Anticancer activity against human HCT15 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
[PMID: 32527536]
HT-29 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human HT-29 cells assessed as reduction in cell viability after 24 hrs by MTT assay
Antiproliferative activity against human HT-29 cells assessed as reduction in cell viability after 24 hrs by MTT assay
[PMID: 26750401]
HT-29 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human HT-29 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Antiproliferative activity against human HT-29 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 26750401]
HT-29 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human HT-29 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Antiproliferative activity against human HT-29 cells assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 26750401]
HT-29 IC50
552 μM
Compound: IB
Cytotoxicity against human HT-29 cells after 72 hrs by MTT assay
Cytotoxicity against human HT-29 cells after 72 hrs by MTT assay
[PMID: 20171760]
Huh-7 IC50
37.2 μM
Compound: Ibu
Cytotoxicity against human HuH7 cells assessed as growth inhibition after 72 hrs by sulforhodamine B assay
Cytotoxicity against human HuH7 cells assessed as growth inhibition after 72 hrs by sulforhodamine B assay
[PMID: 26810835]
K562 IC50
> 1000 μM
Compound: Ibuprofen
Anticancer activity against human K562 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
Anticancer activity against human K562 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
[PMID: 32527536]
L02 IC50
> 100 μM
Compound: Ibuprofen
Antiproliferative activity against human LO2 cells after 72 hrs by CCK-8 assay
Antiproliferative activity against human LO2 cells after 72 hrs by CCK-8 assay
[PMID: 28301815]
MCF7 IC50
> 50 μM
Compound: 6
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability measured after 24 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability measured after 24 hrs by MTT assay
[PMID: 35468536]
MCF7 IC50
> 50 μM
Compound: Ibuprofen
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability measured upto 72 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability measured upto 72 hrs by MTT assay
[PMID: 33799070]
MCF7 IC50
92.14 μM
Compound: Ibuprofen
Anticancer activity against human MCF7 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
Anticancer activity against human MCF7 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
[PMID: 32527536]
MDA-MB-231 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human MDA-MB-231 cells assessed as reduction in cell viability after 24 hrs by MTT assay
Antiproliferative activity against human MDA-MB-231 cells assessed as reduction in cell viability after 24 hrs by MTT assay
[PMID: 26750401]
MDA-MB-231 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human MDA-MB-231 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Antiproliferative activity against human MDA-MB-231 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 26750401]
MDA-MB-231 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human MDA-MB-231 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Antiproliferative activity against human MDA-MB-231 cells assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 26750401]
Neutrophil IC50
12.1 μM
Compound: Ibuprofen
Immunomodulatory activity in polymorphoneutrophils assessed as inhibition of luminol-induced oxidative burst by chemiluminescence assay
Immunomodulatory activity in polymorphoneutrophils assessed as inhibition of luminol-induced oxidative burst by chemiluminescence assay
[PMID: 18950230]
Neutrophil IC50
27.53 μM
Compound: ibuprofen
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP-indcued superoxide production after 5 mins
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP-indcued superoxide production after 5 mins
[PMID: 20839880]
Neutrophil IC50
32.55 μM
Compound: ibuprofen
Antiinflammatory activity in human neutrophils assessed as fMLP-induced superoxide release after 5 mins by spectrometry
Antiinflammatory activity in human neutrophils assessed as fMLP-induced superoxide release after 5 mins by spectrometry
[PMID: 17822293]
PANC-1 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human PANC1 cells assessed as reduction in cell viability after 24 hrs by MTT assay
Antiproliferative activity against human PANC1 cells assessed as reduction in cell viability after 24 hrs by MTT assay
[PMID: 26750401]
PANC-1 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human PANC1 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Antiproliferative activity against human PANC1 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 26750401]
PANC-1 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human PANC1 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Antiproliferative activity against human PANC1 cells assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 26750401]
PC-3 IC50
> 1000 μM
Compound: Ibuprofen
Anticancer activity against human PC3 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
Anticancer activity against human PC3 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
[PMID: 32527536]
PC-3 IC50
> 50 μM
Compound: Ibuprofen
Cytotoxicity against human PC-3 cells assessed as reduction in cell viability measured upto 72 hrs by MTT assay
Cytotoxicity against human PC-3 cells assessed as reduction in cell viability measured upto 72 hrs by MTT assay
[PMID: 33799070]
RAW264.7 IC50
0.39 μM
Compound: Ibuprofen
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-stimulated PGE2 production by ELISA
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-stimulated PGE2 production by ELISA
[PMID: 28408221]
RAW264.7 IC50
0.86 μM
Compound: Ibuprofen
Inhibition of COX-2 in mouse RAW264.7 cells assessed as decrease in LPS-induced PGE2 production treated prior to LPS challenge by enzyme immunoassay
Inhibition of COX-2 in mouse RAW264.7 cells assessed as decrease in LPS-induced PGE2 production treated prior to LPS challenge by enzyme immunoassay
[PMID: 24656662]
RAW264.7 IC50
14.4 μM
Compound: Ibuprofen
Anti-inflammatory activity against LPS-stimulated mouse RAW264.7 cells assessed as reduction in IL1beta protein expression level after 24 hrs by ELISA
Anti-inflammatory activity against LPS-stimulated mouse RAW264.7 cells assessed as reduction in IL1beta protein expression level after 24 hrs by ELISA
[PMID: 34890996]
RAW264.7 IC50
1483.87 μM
Compound: Ibuprofen
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-stimulated NO production by ELISA
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-stimulated NO production by ELISA
[PMID: 28408221]
RAW264.7 IC50
2.1 μM
Compound: Ibuprofen
Anti-inflammatory activity against LPS-stimulated mouse RAW264.7 cells assessed as reduction in TNFalpha protein expression level after 24 hrs by ELISA
Anti-inflammatory activity against LPS-stimulated mouse RAW264.7 cells assessed as reduction in TNFalpha protein expression level after 24 hrs by ELISA
[PMID: 34890996]
RAW264.7 IC50
3309.84 μM
Compound: Ibuprofen
Cytotoxicity against mouse RAW264.7 cells by MTT assay
Cytotoxicity against mouse RAW264.7 cells by MTT assay
[PMID: 28408221]
RAW264.7 IC50
54.5 μM
Compound: Ibuprofen
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production by measuring nitrite accumulation by Griess method
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production by measuring nitrite accumulation by Griess method
[PMID: 28561586]
SK-LU-1 IC50
90.61 μM
Compound: Ibuprofen
Anticancer activity against human SKLU1 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
Anticancer activity against human SKLU1 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
[PMID: 32527536]
TERT-RPE1 IC50
> 40 μM
Compound: 6
Cytotoxicity against human RPE-1 cells assessed as reduction in cell viability measured after 24 hrs by MTT assay
Cytotoxicity against human RPE-1 cells assessed as reduction in cell viability measured after 24 hrs by MTT assay
[PMID: 35468536]
U-251 IC50
> 1000 μM
Compound: Ibuprofen
Anticancer activity against human U251 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
Anticancer activity against human U251 cells assessed as cell growth inhibition measured after 48 hrs by MTT assay
[PMID: 32527536]
UACC-903 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human UACC-903 cells assessed as reduction in cell viability after 24 hrs by MTT assay
Antiproliferative activity against human UACC-903 cells assessed as reduction in cell viability after 24 hrs by MTT assay
[PMID: 26750401]
UACC-903 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human UACC-903 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Antiproliferative activity against human UACC-903 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 26750401]
UACC-903 IC50
> 50 μM
Compound: Ibu
Antiproliferative activity against human UACC-903 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Antiproliferative activity against human UACC-903 cells assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 26750401]
體外研究
(In Vitro)

Ibuprofen(24 小時)抑制 COX-1COX-2 活性,IC50 值分別為 13 μM 和 370 μM[1]
Ibuprofen (500 μM, 48 小時) 抑制細胞增殖和血管生成,并誘導(dǎo) AGS 細胞 (腺癌胃細胞系) 凋亡[2]
Ibuprofen (500 μM, 48 小時) 下調(diào) AGS 細胞中 Akt、VEGF-A、PCNA、Bcl2、OCT3/4 和 CD44 基因的轉(zhuǎn)錄,但上調(diào)野生型 P53 和 Bax 基因的 RNA 水平[2]
Ibuprofen (500 μM, 24 小時) 可恢復(fù)微管重組、微管依賴性細胞內(nèi)膽固醇轉(zhuǎn)運,并誘導(dǎo)囊性纖維化 (CF) 細胞模型和原代 CF 鼻上皮細胞中微管延伸至細胞周圍[3]。
Ibuprofen(500 μM,24 小時)通過光敏化過程增強 MCF-7 細胞和 MDA-MB-231 細胞中紫外線誘導(dǎo)的細胞死亡[4]。

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

Cell Viability Assay[2]

Cell Line: AGS cells
Concentration: 100-1000 μM
Incubation Time: 24 h, 48 h
Result: Inhibited AGS cell viability with IC50 values of 630 μM (trypan blue staining, 24 h), 456 μM (neutral red assay, 24 h), 549 μM (trypan blue staining, 48 h) and 408 μM (neutral red assay, 48 h).
體內(nèi)研究
(In Vivo)

Ibuprofen(300 mg/kg;口服;每日一次,連續(xù) 14 天)在產(chǎn)后乳腺癌模型中減緩了整體腫瘤生長,增強了抗腫瘤免疫特性,且沒有不良的自身免疫反應(yīng)[5]。
Ibuprofen(60 mg/kg;ih;每隔一天一次,持續(xù) 15 天)可降低奧沙利鉑誘發(fā)的慢性周圍神經(jīng)病變大鼠模型中發(fā)生神經(jīng)病變的風(fēng)險[6]。
Ibuprofen(20 mg/kg;口服;每 12 小時一次,共 5 次)會減少肌肉生長(平均肌纖維橫截面積),但不影響岡上肌腱對運動的適應(yīng)性調(diào)節(jié)[7]。
Ibuprofen(35 mg/kg;口服;每日兩次)可減輕大鼠慢性肺部感染模型對銅綠假單胞菌的炎癥反應(yīng)[8]

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

Animal Model: Syngeneic (D2A1) orthotopic Balb/c mouse model of PPBC (postpartum)[5]
Dosage: 300 mg/kg, daily for 14 days
Administration: Fed in animal feedings (added to pulverized standard chow and mixed dry, then mixed with water, made into chow pellets and dried thoroughly)
Result: Suppresed tumor growth, reduced presence of immature monocytes and increased numbers of T cells.
Enhanced Th1 associated cytokines as well as promoted tumor border accumulation of T cells.
Animal Model: Oxaliplatin?induced peripheral neuropathy[6]
Dosage: 60 mg/kg, every second day for 15 days
Administration: Subcutaneous injection
Result: Lowered sensory nerve conduction velocity (SNCV).
Clinical Trial
分子量

206.28

Formula

C13H18O2

CAS 號
性狀

固體

顏色

White to off-white

中文名稱

布洛芬;異丁苯丙酸;異丁洛芬

運輸條件

Room temperature in continental US; may vary elsewhere.

儲存方式

Store at room temperature 3 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 : 100 mg/mL (484.78 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 4.8478 mL 24.2389 mL 48.4778 mL
5 mM 0.9696 mL 4.8478 mL 9.6956 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 (12.12 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。
  • 方案 二

    請依序添加每種溶劑: 10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 2.5 mg/mL (12.12 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 900 μL 20% 的 SBE-β-CD 生理鹽水水溶液 中,混合均勻。

    2 g SBE-β-CD(磺丁基醚 β-環(huán)糊精)粉末定容于 10 mL 的生理鹽水中,完全溶解至澄清透明。
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: 99.97%

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 4.8478 mL 24.2389 mL 48.4778 mL 121.1945 mL
5 mM 0.9696 mL 4.8478 mL 9.6956 mL 24.2389 mL
10 mM 0.4848 mL 2.4239 mL 4.8478 mL 12.1194 mL
15 mM 0.3232 mL 1.6159 mL 3.2319 mL 8.0796 mL
20 mM 0.2424 mL 1.2119 mL 2.4239 mL 6.0597 mL
25 mM 0.1939 mL 0.9696 mL 1.9391 mL 4.8478 mL
30 mM 0.1616 mL 0.8080 mL 1.6159 mL 4.0398 mL
40 mM 0.1212 mL 0.6060 mL 1.2119 mL 3.0299 mL
50 mM 0.0970 mL 0.4848 mL 0.9696 mL 2.4239 mL
60 mM 0.0808 mL 0.4040 mL 0.8080 mL 2.0199 mL
80 mM 0.0606 mL 0.3030 mL 0.6060 mL 1.5149 mL
100 mM 0.0485 mL 0.2424 mL 0.4848 mL 1.2119 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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