Merck
CN
所有图片(1)

文件

安全信息

ACK5010PG

Millipore

Amicon ®Pro Affinity Concentration Kit蛋白G,配备10kDa Amicon® Ultra-0.5设备

Amicon Pro Affinity Concentration Kit Protein G - A Centrifugal Tool for purifying & concentrating Antibodies.

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eCl@ss:
36100101
NACRES:
NB.24

物料

Amicon Ultra styrene-butadiene device
Ultracel® regenerated cellulose membrane (Amicon Ultra-0.5; low binding)
polyethylene cap
polyethylene frit
polypropylene device (for exchange)
polypropylene frit
polypropylene tube (AU0.5; for collection)
polypropylene tube (for collection)
polypropylene tube (holder)

无菌性

non-sterile

产品线

Amicon®

制造商/商品名称

Amicon® Pro

参数

10 mL sample volume

技术

buffer exchange: suitable
protein purification: suitable (antibody labeling)
protein purification: suitable (concentration)
protein purification: suitable (enrichment)

长度

12 cm (4.7 in.)

直径

2.97 cm

过滤面积

1 cm2

孔径

10 kDa NMWCO

运输

wet ice

一般描述

该试剂盒包括12/pk Amicon Pro、12/pk Amicon Ultra NMWCO 10 kDa、3 ml蛋白G树脂(结合容量:20 mg人IgG/ml琼脂糖)、2 X 66 ml结合/清洗缓冲液、12 ml洗脱缓冲液、2.5 ml中和缓冲液
过滤器类型:超滤
过滤器编码:PLCGC

应用

Amicon Pro亲和浓缩试剂盒蛋白G-用于纯化&浓缩抗体的离心工具。

特点和优势

最小最终浓缩体积:15 µL

外形

色码:透明,带有粉色盖

法律信息

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

象形图

FlameCorrosion

警示用语:

Danger

危险声明

危险分类

Flam. Liq. 2 - Met. Corr. 1

储存分类代码

3 - Flammable liquids

WGK

WGK 2

法规信息

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Kevin J Forsberg et al.
Chemistry & biology, 22(7), 888-897 (2015-06-23)
Enzymes capable of inactivating tetracycline are paradoxically rare compared with enzymes that inactivate other natural-product antibiotics. We describe a family of flavoenzymes, previously unrecognizable as resistance genes, which are capable of degrading tetracycline antibiotics. From soil functional metagenomic selections, we
Zahra Seraj et al.
PloS one, 15(5), e0232953-e0232953 (2020-05-20)
The unpleasant smell released from dead bodies, may serve as an alarm for avoiding certain behaviour or as feeding or oviposition attractants for animals. However, little is known about their effect on the structure and function of proteins. Previously, we
Zahra Seraj et al.
Scientific reports, 9(1), 18615-18615 (2019-12-11)
Numerous efforts have been directed towards investigating the different stages leading to the fibrillation process in neurodegenerative diseases and finding the factors modulating it. In this study, using a wide range of molecular techniques as well as fibrillation kinetics coupled

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