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Merck
CN

FCMAB294F

Milli-Mark® Anti-Ubiquitin Antibody, Lys48-Specific-FITC, clone Apu2

clone Apu2, Milli-Mark®, from rabbit

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关于此项目

UNSPSC代码:
12352203
eCl@ss:
32160702
NACRES:
NA.41
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生物来源

rabbit

偶联物

FITC conjugate

抗体形式

purified immunoglobulin

抗体产品类型

primary antibodies

克隆

Apu2, monoclonal

种属反应性

human

制造商/商品名称

Milli-Mark®

技术

flow cytometry: suitable

同位素/亚型

IgG

UniProt登记号

运输

wet ice

靶向翻译后修饰

unmodified

基因信息

human ... UBB(7314)

一般描述

Molecular weight varies
Polyubiquitin chains linked through the Lys48 residue of ubiquitin are most commonly associated with proteins targeted for proteosomal degradation. In contrast, polyubiquitin chains linked through the Lys63 residue of ubiquitin (Ub) are associated with nonproteolytic functions such as signal transduction. Lys63-linked polyUb chains connect components of NFκB signaling in a highly regulated manner, and genetic evidence indicates the involvement of Lys63-linked Ub chains in stress response and DNA repair. Research in yeast has suggested Lys63-linked Ub chains stimulate endocytosis.

免疫原

Epitope: Lys48 ubiquitination site
Immunogen used was di-ubiquitin linked at Lys48

应用

Milli-Mark Anti-Ubiquitin Antibody, Lys48-Specific-FITC, clone Apu2 is an antibody against Ubiquitin for use in FC.
Research Category
Signaling
Research Sub Category
Ubiquitin & Ubiquitin Metabolism

生化/生理作用

Recognizes ubiquitin linked at Lys48. Does not recognize ubiquitin linked at Lys63 or free ubiquitin.

外形

Protein A purified
Purified recombinant rabbit monoclonal IgG conjugated to FITC in PBS with 0.1% sodium azide and 15 mg/mL BSA.

制备说明

Maintain refrigerated at 2-8°C protected from light for up to 6 months from date of receipt.

分析说明

Control
HeLa cells
Evaluated by flow cytometry using HeLa cells

法律信息

MILLI-MARK is a registered trademark of Merck KGaA, Darmstadt, Germany

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Amelia B Karlsson et al.
Molecular biology of the cell, 25(8), 1355-1365 (2014-02-14)
Troyer syndrome is an autosomal recessive hereditary spastic paraplegia (HSP) caused by frameshift mutations in the SPG20 gene that results in a lack of expression of the truncated protein. Spartin is a multifunctional protein, yet only two conserved domains--a microtubule-interacting

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