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Merck
CN

SNAP2MB3

SNAP id® 2.0 Protein Detection System

Double MultiBlot

别名:

蛋白检测系统

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UNSPSC Code:
41116010
eCl@ss:
42029053
NACRES:
NB.22
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产品名称

SNAP i.d. 2.0蛋白质检测系统-双MultiBlot (4.5 x 8.4 cm), Developed to meet the needs of our Western blotting customers, the SNAP i.d. 2.0 system produces blots of a very high quality. Unique vacuum-driven technology & a built-in flow distributor actively drive reagents through the membrane.

manufacturer/tradename

SNAP id®

technique(s)

western blot: suitable

compatibility

for use with Commercially available blocking reagents, for use with Luminata Western HRP Substrates, for use with Nitrocellulose, for use with PVDF (Immobilon membranes), for use with blØk<TMSYMBOL></TMSYMBOL>-CH Buffer (cat. no. WBAVDCH01), for use with blØk<TMSYMBOL></TMSYMBOL>-FL Buffer (cat. no. WBAVDFL01), for use with blØk<TMSYMBOL></TMSYMBOL>-PO Buffer (cat. no. WBAVDP001), for use with commercially available detection reagents

detection method

chemiluminescent, colorimetric, fluorometric

shipped in

ambient

storage temp.

room temp

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General description

该系统包括SNAP i.d. 2.0底座,两个多印迹固定架,两个抗体收集托盘,真空管,滚动垫&印迹辊,两个润湿托盘和一个快速入门指南

Application

为满足我们的蛋白质印迹法客户的需求而开发的SNAP i.d. 2.0系统会产生非常高质量的印迹。独特的真空驱动技术 & 内置流量分配器主动驱动试剂通过膜。
用于免疫印迹检测。

Other Notes

替代品:WBAVDBASE

Legal Information

SNAP id is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。

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商品

Understand the importance of using high-quality water in protein electrophoresis and Western blotting to improve assay sensitivity and accuracy.

实验方案

The SNAP i.d. 2.0 Protein Detection System is the second generation of the SNAP i.d. method for detecting immunoreactive proteins on Western blots.

相关内容

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We get it. Westerns can be a pain in the blot, and we’ve certainly made our share. So, share with us your ugly blots and receive a surprise! And while we can’t tell you what it is – that would spoil the surprise - except that it will spark creativity in the lab.

Two attributes of the Amicon® Pro device make it a convenient device for preparing pure, labeled antibody. First, the device enables highly efficient buffer exchange via diafiltration with simultaneous sample concentration in a single 15 minute spin. Second, the entire workflow can be performed within a single device, reducing the potential for sample loss. In this report, we describe the successful use of the Amicon® Pro device for small–scale biotinylation of a target antibody. The biotinylated antibody was used for detection of protein immunoprecipitated from cell lysate.

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