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Key Documents

MATRNPS50

Millipore

96孔收集板

Clear, Non-Sterile, Transport Receiver Plate, 100uL volume, 50 plates, Styrene

别名:

96-well plate, Microplate

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About This Item

分類程式碼代碼:
41104923
eCl@ss:
32039006
NACRES:
NB.22

材料

polystyrene

品質等級

無菌

non-sterile

產品線

MultiScreen®

製造商/商標名

MultiScreen®

參數

100 μL sample volume (per well)

技術

cell culture | mammalian: suitable
parallel artificial membrane permeation assay (PAMPA): suitable

板尺寸

96 wells

運輸包裝

ambient

一般說明

带有接收板的MultiScreen-Mesh板提供了一个完整的系统,用于一步方案中的培养、检验和读取分析结果。该系统非常适合使用多细胞生物作为体内模型评估新化合物的靶标筛选和其他应用。

MultiScreen-Mesh优化了96孔格式的化合物和靶标识别。96孔尼龙网板和96孔托盘配合在一起,为测量多细胞生物的麻痹、细胞毒性和死亡的测定提供了即用型系统。从适合您应用的补片孔径范围中进行选择。简单地将寄生虫、线虫或其他多细胞生物转移到孔中,用目标化合物处理,并测量生物体的迁移。平板光学透明,可与成像显微镜或其他显微镜分析一起使用。如果需要,可以在平板上涂上一层薄层琼脂。

在FACS分析仪中进行细胞分析之前,MultiScreen-Mesh板也已被证明可用作高通量细胞过滤网。为了在将平板加载到FACS仪器之前解离细胞团块,可以通过重力流或通过轻轻离心将细胞悬浮液通过筛孔板运行。

该滤板提供了一个完整的系统,可用于一步方案中的培养、检验和读取分析结果。该系统是目标筛选和其他评估新化合物对整个多细胞生物影响的应用的理想选择。对MultiScreen-Mesh滤板进行了优化,以96孔格式识别化合物和靶标。滤板和96孔托盘配合在一起,为测量多细胞生物的麻痹、细胞毒性和死亡的测定提供了即用型系统。只需将寄生虫、线虫或其他多细胞生物转移到孔中,用目标化合物处理,并测量生物体的迁移。

功能&优势:
- 多种配置和应用
- 化学相容性
- 自动化相容性
- 卓越的真空过滤和滤液收集
- 平板光学透明,可与成像显微镜或其他显微分析一起使用

应用
- 全生物体筛选

應用

研究类别
细胞培养

蛋白质

外觀

色码:透明

其他說明

自动化兼容:否

法律資訊

MULTISCREEN is a registered trademark of Merck KGaA, Darmstadt, Germany

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商品

This is a white paper on the Evaluation of the reproducibility of Parallel Artificial Membrane Permeation Assays (PAMPA) using MultiScreen® Filter Plates.

This is a protocol for a Membrane Integrity test for Lipid-PAMPA Artificial Membranes

Combining solubility & PAMPA assays streamlines drug permeability testing.

Combining solubility & PAMPA assays streamlines drug permeability testing.

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实验方案

Assays that predict passive absorption of orally administered drugs have become increasingly important in the drug discovery process. As previously described by Faller and Kansy such assays provide rapid, low cost and automation friendly methods to measure a compound’s passive permeability.

Assays that predict passive absorption of orally administered drugs have become increasingly important in the drug discovery process. As previously described by Faller and Kansy such assays provide rapid, low cost and automation friendly methods to measure a compound’s passive permeability.

Assays that predict passive absorption of orally administered drugs have become increasingly important in the drug discovery process. As previously described by Faller and Kansy such assays provide rapid, low cost and automation friendly methods to measure a compound’s passive permeability.

Assays that predict passive absorption of orally administered drugs have become increasingly important in the drug discovery process. As previously described by Faller and Kansy such assays provide rapid, low cost and automation friendly methods to measure a compound’s passive permeability.

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