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Merck
CN

SNAP2BHMB050

Millipore

SNAP id® 2.0 MultiBlot Holders

4.5 x 8.4 cm, horizontal, flat profile for compact space storage

别名:

Western blot, Western blot holders, blot holders

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关于此项目

UNSPSC代码:
41116010
eCl@ss:
42029053
NACRES:
NA.32
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产品名称

SNAP id® 2.0 MultiBlot支架(4.5 x 8.4 cm), The new MultiBlot Holders ensure that each half blot membrane is aligned horizontally, allowing for the uniform distribution of antibody. The flat profile alows for compact space allocation for storage, shipping and waste management.

质量水平

制造商/商品名称

SNAP id®

技术

western blot: suitable

相容性

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

检测方法

chemiluminescent
colorimetric
fluorometric

运输

ambient

储存温度

room temp

应用

用于免疫印迹检测。

法律信息

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

免责声明

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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实验方案

Western blot protocol details protein transfer from gels to nitrocellulose, crucial for immunoblotting procedures in research.

带有用于不同印迹过程工作流程步骤的Western blot实验方法,描述了蛋白从SDS聚丙烯酰胺凝胶(SDS-PAGE)到硝酸纤维素膜(NC膜)的电泳转移。也称为免疫印迹实验方法。

相关内容

There’s so much room for experimental variability in traditional immunodetection workflows. For your peace of mind – and ours – we designed the SNAP i.d.® 2.0 system to streamline your Western blot and immunohistochemistry experiments. The concept is simple: a vacuum-driven flow of blocking, antibody, and washing solutions reduces slide and membrane handling. That means a lot less shaking, dipping, pouring and waiting. And now you can process multiple blots and slides in parallel, so it’s easy to apply consistent conditions across experiments.

Antibody reuse for Western blotting is a common practice for many researchers. While many antibodies lose potency with time or degrade even faster due to improper storage conditions, it is important to recognize the potential value of recovering the primary antibody for possible reuse in some experiments. The SNAP i.d.® 2.0 system is not only able to reduce the immunodetection processing time, but its flexibility lets you combine conditions used in the standard immunodetection protocol and also allows the collection of antibody for future reuse. Here, we compare the antibody recovery and reuse in the standard immunodetection protocol with the antibody recovery and reuse in SNAP i.d.® system using the extended protocol and the original SNAP i.d.® protocol.

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