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重要文件

06-1130

Sigma-Aldrich

Anti-RNF168 Antibody

同義詞:

E3 ubiquitin-protein ligase RNF168, RING finger protein 168

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About This Item

分類程式碼代碼:
12352203
eCl@ss:
32160702

生物源

rabbit

抗體表格

affinity isolated antibody

無性繁殖

polyclonal

純化經由

affinity chromatography

物種活性

human

技術

immunoprecipitation (IP): suitable
western blot: suitable

NCBI登錄號

UniProt登錄號

一般說明

RNF168 is a ubiquitin ligand that binds to ubiquinated histone H2A and localizes to sites of DNA damage. RNF168-dependent chromatin modifications cause 53BP1 and BRCA1 to accumulated at the site. A mutation in RNF168 has been associated with RIDDLE syndrome, an immunodeficiency and radiosensitivity disorder. RNF168 is responsible for securing repair factors at sites of DNA damage. RNF168 has two MIU (motif interacting with ubiquitin) and one UMI (UIM- and MIU-related UBD) ubiquitin binding domains (UBDs) which are essential for proper localization of RNF168.

特異性

This antibody recognizes RNF168 at the C-terminus.

免疫原

Histidine-tagged recombinant protein corresponding to the C-terminus of human RNF168.

應用

Anti-RNF168 Antibody is a Rabbit Polyclonal Antibody for detection of RNF168 also known as E3 ubiquitin-protein ligase RNF168 & has been validated in WB.
Immunoprecipitation Analysis: A representative lot of this antibody was used to immunoprecipitate RNF168 from whole cell lysates (Zhao, H., et al. (2014) Cell Cycle. 13(11):1–11).
Research Category
Epigenetics & Nuclear Function
Research Sub Category
Chromatin Biology

品質

Evaluated by Western Blot in Jurkat cell lysate.

Western Blot Analysis: 0.1 μg/mL of this antibody detected RNF168 on 10 μg of Jurkat cell lysate.

標靶描述

~79 kDa observed.

外觀

Purified rabbit polyclonal in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

儲存和穩定性

Stable for 1 year at 2-8°C from date of receipt.

分析報告

Control
Jurkat cell lysate

其他說明

Concentration:Please refer to the Certificate of Analysis for the lot-specific concentration.

免責聲明

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

儲存類別代碼

10-13 - German Storage Class 10 to 13


分析證明 (COA)

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Hongchang Zhao et al.
Cell cycle (Georgetown, Tex.), 13(11), 1777-1787 (2014-04-16)
Timely and proper cellular response to DNA damage is essential for maintenance of genome stability and integrity. B-cell lymphoma/leukemia 10 (BCL10) facilitates ubiquitination of NEMO in the cytosol, activating NFκB signaling. Translocation and/or point mutations of BCL10 associate with mucosa-associated
Katherine N Choe et al.
EMBO reports, 17(6), 874-886 (2016-05-06)
Defects in DNA replication, DNA damage response, and DNA repair compromise genomic stability and promote cancer development. In particular, unrepaired DNA lesions can arrest the progression of the DNA replication machinery during S-phase, causing replication stress, mutations, and DNA breaks.
Meilen C Muñoz et al.
The Journal of biological chemistry, 287(48), 40618-40628 (2012-10-12)
RNF168 promotes chromosomal break localization of 53BP1 and BRCA1; 53BP1 loss rescues homologous recombination (HR) in BRCA1-deficient cells. RNF168 depletion suppresses HR defects caused by BRCA1 silencing; RNF168 influences HR similarly to 53BP1. RNF168 is important for HR defects caused
Kathy Shire et al.
Journal of cell science, 129(3), 580-591 (2015-12-18)
Promyelocytic leukemia (PML) protein forms the basis of PML nuclear bodies (PML NBs), which control many important processes. We have screened an shRNA library targeting ubiquitin pathway proteins for effects on PML NBs, and identified RNF8 and RNF168 DNA-damage response
Lianzhong Zhang et al.
Genomics, proteomics & bioinformatics, 16(6), 428-438 (2018-12-12)
DNA damage response (DDR) is essential for maintaining genome stability and protecting cells from tumorigenesis. Ubiquitin and ubiquitin-like modifications play an important role in DDR, from signaling DNA damage to mediating DNA repair. In this report, we found that the

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