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Merck
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文件

MAUF01005

Millipore

MultiScreen® 96孔超滤板,带Ultracel®-10膜kD

别名:

96-well centrifuge concentrator

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About This Item

分類程式碼代碼:
41104923
NACRES:
NB.24

材料

polypropylene plate
regenerated cellulose (RC)
silicone O-ring (medical grade)

描述

For sample purification, concentration and desalting of biological solutions or protein removal

無菌

non-sterile

製造商/商標名

MultiScreen®

高度

20.1 mm , without lid
22.0 mm , with lid

長度

127.8 mm

容積

0.5 mL

寬度

85.5 mm

孔徑

10 kDa NMWCO

儲存溫度

room temp

一般說明

带Ultracel®膜的MultiScreen® 96孔超滤板(MultiScreen超滤板)用于处理生物水溶液(0.1至0.5 mL)。超滤板仅在离心压力模式下使用,并与标准离心机微量滴定板摆动斗转子兼容。它旨在配合用于超滤液收集的96孔微滴度接收板。这些板是设计用于样品分析前的蛋白质去除和样品纯化、浓缩和生物溶液脱盐。 
Reliability
The 96-well MultiScreen® filter plate incorporates Ultracel® -10 10,000 kDa nominal molecular weight limit regenerated cellulose ultrafiltration membrane for low-binding, high recovery results. It is designed for use with centrifugation and is compatible with standard microtiter plates, instrumentation, and liquid handling equipment.

MultiScreen® filter plate with Ultracel® -10 membrane is designed for low protein binding and high protein retention. The assay-grade plates meet stringent manufacturing release specifications and are lot tested for protein retention for >95% retention of cytochrome c (12,500 Daltons). They also offer high well-to-well uniformity of performance.

Versatile Operation
MultiScreen® filter plates with Ultracel® -10 membrane allow for processing and collection of sample volumes from 50 to 500 µL. They are compatible with a range of standard receiver 96-well microtiter plates including 300 µL, 700 µL deep well and 150 µL conical well.

應用

带Ultracel®-10膜kD的MultiScreen® 96孔超滤板适用于高通量蛋白浓缩和缓冲交换。

外觀

色码:自然

法律資訊

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

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Priscilla A Moore et al.
Methods in molecular biology (Clifton, N.J.), 498, 309-314 (2008-11-07)
High-throughput protein purification is a complex, multi-step process. There are several technical challenges in the course of this process that are not experienced when purifying a single protein. Among the most challenging are the high-throughput protein concentration and buffer exchange

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