06-1130
Anti-RNF168 Antibody
Synonym(s):
E3 ubiquitin-protein ligase RNF168, RING finger protein 168
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About This Item
eCl@ss:
32160702
UNSPSC Code:
12352203
biological source
rabbit
antibody form
affinity isolated antibody
clone
polyclonal
purified by
affinity chromatography
species reactivity
human
technique(s)
immunoprecipitation (IP): suitable, western blot: suitable
NCBI accession no.
UniProt accession no.
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General description
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.
~79 kDa observed.
Immunogen
Histidine-tagged recombinant protein corresponding to the C-terminus of human RNF168.
Application
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
Epigenetics & Nuclear Function
Research Sub Category
Chromatin Biology
Chromatin Biology
Biochem/physiol Actions
This antibody recognizes RNF168 at the C-terminus.
Physical form
Purified rabbit polyclonal in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.
Preparation Note
Stable for 1 year at 2-8°C from date of receipt.
Analysis Note
Control
Jurkat cell lysate
Jurkat cell lysate
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.
Western Blot Analysis: 0.1 μg/mL of this antibody detected RNF168 on 10 μg of Jurkat cell lysate.
Other Notes
Concentration:Please refer to the Certificate of Analysis for the lot-specific concentration.
Disclaimer
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
Storage Class
10-13 - German Storage Class 10 to 13
Regulatory Information
新产品
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Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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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.
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
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
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
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