1. Anti-infection Apoptosis Autophagy
  2. HIV Reverse Transcriptase Apoptosis Autophagy
  3. Dapivirine

Dapivirine  (Synonyms: 达匹维林; TMC120; R147681)

目录号: HY-14266 纯度: 99.80%
COA 产品使用指南 技术支持

Dapivirine (TMC120) 是二芳基嘧啶 (DAPY) 的原型,是具有口服活性的非核苷类逆转录酶抑制剂 (NRTI)。Dapivirine (TMC120) 可直接与 HIV 的逆转录酶结合。Dapivirine (TMC120)调节自噬并诱导 Akt、Bad 和 SAPK/JNK 的激活。

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Dapivirine Chemical Structure

Dapivirine Chemical Structure

CAS No. : 244767-67-7

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规格 价格 是否有货 数量
10 mM * 1 mL in DMSO ¥399
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1 mg ¥245
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5 mg ¥550
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10 mg ¥900
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25 mg ¥1650
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50 mg ¥2475
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100 mg ¥3500
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500 mg   询价  

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Customer Review

Other Forms of Dapivirine:

查看 HIV 亚型特异性产品:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Dapivirine (TMC120), the prototype of diarylpyrimidines (DAPY), is an orally active and nonnucleoside reverse transcriptase inhibitor (NRTI). Dapivirine (TMC120) binds directly to HIV-1 reverse transcriptase. Dapivirine (TMC120) regulates autophagy and induced Akt, Bad and SAPK/JNK activations[1][2].

IC50 & Target

HIV-1

 

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
Caco-2 IC50
0.73 μM
Compound: DAPIVIRINE
Determination of IC50 values for inhibition of SARS-CoV-2 induced cytotoxicity of Caco-2 cells after 48 hours by high content imaging
Determination of IC50 values for inhibition of SARS-CoV-2 induced cytotoxicity of Caco-2 cells after 48 hours by high content imaging
10.21203/rs.3.rs-23951/v1
Caco-2 CC50
5 μM
Compound: DAPIVIRINE
Toxicity against Caco-2 cells determined at 48 hours by intracellular ATP concentration using the CellTiter-Glo Luminescent Cell Viability Assay
Toxicity against Caco-2 cells determined at 48 hours by intracellular ATP concentration using the CellTiter-Glo Luminescent Cell Viability Assay
10.21203/rs.3.rs-23951/v1
Macrophage CC50
> 20000 nM
Compound: dapivirine
Cytotoxicity against human monocyte derived macrophages after 24 hrs by MTT assay
Cytotoxicity against human monocyte derived macrophages after 24 hrs by MTT assay
[PMID: 19029331]
MRC5 IC50
> 64 μM
Compound: 1, TMC120
Cytotoxicity against human MRC5 SV2 cells assessed as reduction in cell growth after 72 hrs
Cytotoxicity against human MRC5 SV2 cells assessed as reduction in cell growth after 72 hrs
[PMID: 25199582]
MRC5 IC50
1.25 μM
Compound: 1, TMC120
Trypanocidal activity against nifurtimox-sensitive Trypanosoma cruzi Tulahuen CL2 infected in human MRC5 SV2 cells assessed as parasite growth inhibition after 168 hrs by beta-galactosidase assay
Trypanocidal activity against nifurtimox-sensitive Trypanosoma cruzi Tulahuen CL2 infected in human MRC5 SV2 cells assessed as parasite growth inhibition after 168 hrs by beta-galactosidase assay
[PMID: 25199582]
MT2 EC50
0.0007 μM
Compound: 8a, TMC120
Antiviral activity against wild type HIV1 3B infected in human MT2 cells assessed as protection against virus-induced effect by MTT assay
Antiviral activity against wild type HIV1 3B infected in human MT2 cells assessed as protection against virus-induced effect by MTT assay
[PMID: 23937980]
MT2 EC50
0.039 μM
Compound: 8a, TMC120
Antiviral activity against HIV1 3B harboring reverse transcriptase K103N/Y181C double mutant infected in human MT2 cells assessed as protection against virus-induced effect by MTT assay
Antiviral activity against HIV1 3B harboring reverse transcriptase K103N/Y181C double mutant infected in human MT2 cells assessed as protection against virus-induced effect by MTT assay
[PMID: 23937980]
MT2 EC50
0.039 μM
Compound: 8a, TMC120
Antiviral activity against HIV1 3B harboring reverse transcriptase Y181C mutant infected in human MT2 cells assessed as protection against virus-induced effect by MTT assay
Antiviral activity against HIV1 3B harboring reverse transcriptase Y181C mutant infected in human MT2 cells assessed as protection against virus-induced effect by MTT assay
[PMID: 23937980]
MT2 CC50
1.9 μM
Compound: TMC120
Cytotoxicity against human MT2 cells after 5 days by MTT assay
Cytotoxicity against human MT2 cells after 5 days by MTT assay
[PMID: 24900627]
MT4 EC50
> 20 μM
Compound: TMC120
Antiviral activity against TMC120-resistant HIV1 harboring RT 100I, 138G mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
Antiviral activity against TMC120-resistant HIV1 harboring RT 100I, 138G mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
[PMID: 24805780]
MT4 EC50
> 20 μM
Compound: TMC120
Antiviral activity against TMC125-resistant HIV1 harboring RT 109M, 138K, 190E mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
Antiviral activity against TMC125-resistant HIV1 harboring RT 109M, 138K, 190E mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
[PMID: 24805780]
MT4 EC50
0.001 μM
Compound: TMC120
Antiviral activity against zidovudine-resistant HIV1 harboring RT 67N, 70R, 215F, 219Q mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
Antiviral activity against zidovudine-resistant HIV1 harboring RT 67N, 70R, 215F, 219Q mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
[PMID: 24805780]
MT4 EC50
0.002 μM
Compound: TMC120
Antiviral activity against MDR-resistant HIV1 harboring 41L, 74V, 106A, 215Y mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
Antiviral activity against MDR-resistant HIV1 harboring 41L, 74V, 106A, 215Y mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
[PMID: 24805780]
MT4 EC50
0.003 μM
Compound: TMC120
Antiviral activity against wild type HIV1 3B infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
Antiviral activity against wild type HIV1 3B infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
[PMID: 24805780]
MT4 EC50
0.003 μM
Compound: TMC120
Antiviral activity against saquinavir-resistant HIV1 infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
Antiviral activity against saquinavir-resistant HIV1 infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
[PMID: 24805780]
MT4 EC50
0.03 nM
Compound: TMC120
Antiviral activity against wild type HIV 1 NL4-3 infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antiviral activity against wild type HIV 1 NL4-3 infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 21438533]
MT4 EC50
0.04 μM
Compound: TMC120
Antiviral activity against N119-sensitive HIV1 harboring Y181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
Antiviral activity against N119-sensitive HIV1 harboring Y181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
[PMID: 24805780]
MT4 EC50
0.05 μM
Compound: TMC120
Antiviral activity against A17-sensitive HIV1 harboring 103N, 181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
Antiviral activity against A17-sensitive HIV1 harboring 103N, 181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
[PMID: 24805780]
MT4 EC50
0.1 μM
Compound: TMC120
Antiviral activity against 6-[(3,5-Dimethylphenyl)fluoromethyl]-5-ethyl-1-{[[4-(3-hydroxyprop-1-ynyl)benzyl]oxy]methyl}pyrimidine-2,4(1H,3H)-dione-resistant HIV1 harboring RT 106I, 181C mutant infected in human MT4 cells assessed as inhibition of virus-in
Antiviral activity against 6-[(3,5-Dimethylphenyl)fluoromethyl]-5-ethyl-1-{[[4-(3-hydroxyprop-1-ynyl)benzyl]oxy]methyl}pyrimidine-2,4(1H,3H)-dione-resistant HIV1 harboring RT 106I, 181C mutant infected in human MT4 cells assessed as inhibition of virus-in
[PMID: 24805780]
MT4 EC50
0.1 μM
Compound: TMC120
Antiviral activity against MC1220-resistant HIV1 harboring RT 100I, 179D, 181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
Antiviral activity against MC1220-resistant HIV1 harboring RT 100I, 179D, 181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
[PMID: 24805780]
MT4 EC50
0.2 μM
Compound: TMC120
Antiviral activity against efavirenz-resistant HIV1 harboring RT 100I, 103R, 179D, 225H mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
Antiviral activity against efavirenz-resistant HIV1 harboring RT 100I, 103R, 179D, 225H mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity after 4 days by MTT assay
[PMID: 24805780]
MT4 EC50
0.3 nM
Compound: TMC120
Antiviral activity against multidrug-resistant HIV 1 IRLL98 harboring reverse transcriptase K101Q/Y181C/G190a mutant infected in human MT4 cells assessed as virus-induced cytopathic effect after 5 days by MTT assay
Antiviral activity against multidrug-resistant HIV 1 IRLL98 harboring reverse transcriptase K101Q/Y181C/G190a mutant infected in human MT4 cells assessed as virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 21438533]
MT4 EC50
0.6 nM
Compound: TMC120
Antiviral activity against wild type HIV1 NL4-3 infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antiviral activity against wild type HIV1 NL4-3 infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 22428851]
MT4 IC50
0.9 nM
Compound: dapivirine
Antiviral activity against HIV-1 3B infected in human MT4 cells after 7 days by RT assay
Antiviral activity against HIV-1 3B infected in human MT4 cells after 7 days by RT assay
[PMID: 19029331]
MT4 EC50
1.2 nM
Compound: TMC120
Antiviral activity against HIV1 harboring reverse transcriptase K103N mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antiviral activity against HIV1 harboring reverse transcriptase K103N mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 22428851]
MT4 EC50
1.2 nM
Compound: TMC120
Antiviral activity against HIV1 harboring reverse transcriptase Y181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antiviral activity against HIV1 harboring reverse transcriptase Y181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 22428851]
MT4 EC50
1.2 nM
Compound: TMC120
Antiviral activity against HIV 1 harboring reverse transcriptase K103N mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antiviral activity against HIV 1 harboring reverse transcriptase K103N mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 21438533]
MT4 EC50
1.2 nM
Compound: TMC120
Antiviral activity against HIV 1 harboring reverse transcriptase Y181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antiviral activity against HIV 1 harboring reverse transcriptase Y181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 21438533]
MT4 CC50
2 μM
Compound: TMC120
Cytotoxicity against human MT4 cells after 96 hrs by MTT assay
Cytotoxicity against human MT4 cells after 96 hrs by MTT assay
[PMID: 24805780]
MT4 CC50
2150 nM
Compound: dapivirine
Cytotoxicity against human MT4 cells after 24 hrs by MTT assay
Cytotoxicity against human MT4 cells after 24 hrs by MTT assay
[PMID: 19029331]
MT4 CC50
3000 nM
Compound: TMC120
Cytotoxicity against human MT4 cells assessed as reduction in cell viability after 5 days by MTT assay
Cytotoxicity against human MT4 cells assessed as reduction in cell viability after 5 days by MTT assay
[PMID: 30525601]
MT4 CC50
3000 nM
Compound: TMC120
Cytotoxicity against human MT4 cells after 5 days by MTT assay
Cytotoxicity against human MT4 cells after 5 days by MTT assay
[PMID: 22428851]
MT4 CC50
3035.8 nM
Compound: TMC120
Cytotoxicity against human MT4 cells assessed as cell viability by MTT assay
Cytotoxicity against human MT4 cells assessed as cell viability by MTT assay
[PMID: 21438533]
MT4 EC50
330 nM
Compound: TMC120
Antiviral activity against HIV1 harboring reverse transcriptase Y188L mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antiviral activity against HIV1 harboring reverse transcriptase Y188L mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 22428851]
MT4 EC50
333.9 nM
Compound: TMC120
Antiviral activity against HIV 1 harboring reverse transcriptase Y188L mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antiviral activity against HIV 1 harboring reverse transcriptase Y188L mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 21438533]
TZM CC50
2.47 μM
Compound: 1, TMC120
Cytotoxicity against human TZM-bl cells assessed as cell viability after 48 hrs by WST1 assay
Cytotoxicity against human TZM-bl cells assessed as cell viability after 48 hrs by WST1 assay
[PMID: 25199582]
TZM CC50
2.88 μM
Compound: 6, TMC120, Dapivirine
Cytotoxicity against human TZM-b1 cells infected with wild type HIV1 BaL after 48 hrs using formazan dye by WST1 assay
Cytotoxicity against human TZM-b1 cells infected with wild type HIV1 BaL after 48 hrs using formazan dye by WST1 assay
[PMID: 21930388]
TZM CC50
20400 nM
Compound: dapivirine
Cytotoxicity against human TZM-bl cells after 24 hrs by MTT assay
Cytotoxicity against human TZM-bl cells after 24 hrs by MTT assay
[PMID: 19029331]
TZM CC50
3.4 μM
Compound: TMC120
Cytotoxicity against human TZM-bl cells assessed as reduction in cell viability after 2 days by WST-1 assay
Cytotoxicity against human TZM-bl cells assessed as reduction in cell viability after 2 days by WST-1 assay
[PMID: 26898379]
体外研究
(In Vitro)

Dapivirine (4-64 μM,24、48、72、96 和 120 小时) 抑制胶质瘤细胞增殖并诱导细胞凋亡 (16 μM,12-48 小时)[1]
Dapivirine (8 和 16 μM,12 h) 增强胶质瘤细胞的侵袭[1]
Dapivirine (16 μM,12 h,24 h 和 48 h) 促进 U87 细胞自噬[1]
Dapivirine (TMC120-R147681) 在 10 nM 浓度下明显阻断原代培养物中的感染,但二次培养物显示需要 100 nM 浓度才能完全阻止前病毒整合[3]

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

Cell Proliferation Assay[1]

Cell Line: U87 glioblastoma cells.
Concentration: 4, 8, 16 μM.
Incubation Time: 24, 48, 72, 96 and 120 hours.
Result: Inhibited proliferation of glioma cells.
IC50 was 10.73 μM.

Apoptosis Analysis[1]

Cell Line: U87 glioblastoma cells.
Concentration: 16 μM.
Incubation Time: 12h, 24h and 48h.
Result: Induced apoptosis.
Decreased caspase-3.
体内研究
(In Vivo)

Dapivirine (16 mg/kg,每 3 天一次,持续 12 天) 在小鼠人胶质母细胞瘤模型中表现出强大的抗肿瘤活性[1]
Dapivirine 已被证明具有半衰期在 65 至 90 小时范围内[4]

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

Animal Model: U87 cells were subcutaneously injected into the nude mice[1].
Dosage: 16 mg/kg.
Administration: Once every 3 days for 12 days.
Result: Significantly decreased the tumor volumes.
A significant decrease in Ki67 (a marker for proliferating cells that is overexpressed in many cancers) staining in sections of dapivirine-treated tumors compared to tumors from vehicle-treated mice.
Clinical Trial
分子量

329.41

Formula

C20H19N5

CAS 号
性状

固体

颜色

White to off-white

中文名称

达匹维林

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 2 years
-20°C 1 year
溶解性数据
细胞实验: 

DMSO 中的溶解度 : ≥ 47 mg/mL (142.68 mM; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

* "≥" means soluble, but saturation unknown.

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 3.0358 mL 15.1788 mL 30.3576 mL
5 mM 0.6072 mL 3.0358 mL 6.0715 mL
查看完整储备液配制表

* 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, 2 years; -20°C, 1 year。-80°C储存时,请在2年内使用, -20°C储存时,请在1年内使用。

  • 摩尔计算器

  • 稀释计算器

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

质量
=
浓度
×
体积
×
分子量 *

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

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物实验:

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

  • 方案 一

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

    Solubility: 2.08 mg/mL (6.31 mM); 悬浊液; 超声助溶

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

    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;再向上述体系中加入 50 μL Tween-80,混合均匀;然后再继续加入 450 μL 生理盐水 定容至 1 mL

    生理盐水的配制:将 0.9 g 氯化钠,溶解于 ddH₂O 并定容至 100 mL,可以得到澄清透明的生理盐水溶液。
  • 方案 二

    请依序添加每种溶剂: 10% DMSO    90% Corn Oil

    Solubility: ≥ 2.08 mg/mL (6.31 mM); 澄清溶液

    此方案可获得 ≥ 2.08 mg/mL(饱和度未知)的澄清溶液,此方案实验周期在半个月以上的动物实验酌情使用。

    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。

动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
请输入您的动物体内配方组成:
%
DMSO +
+
%
Tween-80 +
%
Saline
如果您的动物是免疫缺陷鼠或者体弱鼠,建议 DMSO 中的在最后工作液体系中的占比尽量不超过 2%。
方案所需 助溶剂 包括:DMSO ,均可在 MCE 网站选购。 Tween 80,均可在 MCE 网站选购。
计算结果
工作液所需浓度 : mg/mL
储备液配制方法 : mg 药物溶于 μL  DMSO(母液浓度为 mg/mL)。
您所需的储备液浓度超过该产品的实测溶解度,以下方案仅供参考,如有需要,请与 MCE 中国技术支持联系。
动物实验体内工作液的配制方法 : 取 μL DMSO 储备液,加入 μL  μL ,混合均匀至澄清,再加 μL Tween 80,混合均匀至澄清,再加 μL 生理盐水
连续给药周期超过半月以上,请谨慎选择该方案。
请确保第一步储备液溶解至澄清状态,从左到右依次添加助溶剂。您可采用超声加热 (超声清洗仪,建议频次 20-40 kHz),涡旋吹打等方式辅助溶解。
纯度 & 产品资料

纯度: 99.80%

参考文献

完整储备液配制表

* 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, 2 years; -20°C, 1 year。-80°C储存时,请在2年内使用, -20°C储存时,请在1年内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 3.0358 mL 15.1788 mL 30.3576 mL 75.8940 mL
5 mM 0.6072 mL 3.0358 mL 6.0715 mL 15.1788 mL
10 mM 0.3036 mL 1.5179 mL 3.0358 mL 7.5894 mL
15 mM 0.2024 mL 1.0119 mL 2.0238 mL 5.0596 mL
20 mM 0.1518 mL 0.7589 mL 1.5179 mL 3.7947 mL
25 mM 0.1214 mL 0.6072 mL 1.2143 mL 3.0358 mL
30 mM 0.1012 mL 0.5060 mL 1.0119 mL 2.5298 mL
40 mM 0.0759 mL 0.3795 mL 0.7589 mL 1.8973 mL
50 mM 0.0607 mL 0.3036 mL 0.6072 mL 1.5179 mL
60 mM 0.0506 mL 0.2530 mL 0.5060 mL 1.2649 mL
80 mM 0.0379 mL 0.1897 mL 0.3795 mL 0.9487 mL
100 mM 0.0304 mL 0.1518 mL 0.3036 mL 0.7589 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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产品名称:
Dapivirine
目录号:
HY-14266
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