Recombinant Mouse Rnf168 Protein, Myc/DDK-tagged
Cat.No. : | Rnf168-5551M |
Product Overview : | Purified recombinant protein of mouse full-length ring finger protein 168 (Rnf168), with C-terminal MYC/DDK tag, expressed in HEK293T cells. |
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Description : | E3 ubiquitin-protein ligase required for accumulation of repair proteins to sites of DNA damage. Acts with UBE2N/UBC13 to amplify the RNF8-dependent histone ubiquitination. Recruited to sites of DNA damage at double-strand breaks (DSBs) by binding to ubiquitinated histone H2A and H2AX and amplifies the RNF8-dependent H2A ubiquitination, promoting the formation of 'Lys-63'-linked ubiquitin conjugates. This leads to concentrate ubiquitinated histones H2A and H2AX at DNA lesions to the threshold required for recruitment of TP53BP1 and BRCA1. Also recruited at DNA interstrand cross-links (ICLs) sites and promotes accumulation of 'Lys-63'-linked ubiquitination of histones H2A and H2AX, leading to recruitment of FAAP20 and Fanconi anemia (FA) complex, followed by interstrand cross-link repair. H2A ubiquitination also mediates the ATM-dependent transcriptional silencing at regions flanking DSBs in cis, a mechanism to avoid collision between transcription and repair intermediates. Also involved in class switch recombination in immune system, via its role in regulation of DSBs repair. Following DNA damage, promotes the ubiquitination and degradation of JMJD2A/KDM4A in collaboration with RNF8, leading to unmask H4K20me2 mark and promote the recruitment of TP53BP1 at DNA damage sites. Not able to initiate 'Lys-63'-linked ubiquitination in vitro; possibly due to partial occlusion of the UBE2N/UBC13-binding region. Catalyzes monoubiquitination of 'Lys-13' and 'Lys-15' of nucleosomal histone H2A (H2AK13Ub and H2AK15Ub, respectively). |
Source : | HEK293T |
Species : | Mouse |
Tag : | Myc&DDK |
Molecular Mass : | 61 kDa |
Purity : | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Stability : | Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Storage : | Store at -80 centigrade after receiving vials. |
Concentration : | >50 μg/mL as determined by microplate BCA method |
Storage Buffer : | 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol. |
Gene Name : | Rnf168 ring finger protein 168 [ Mus musculus (house mouse) ] |
Official Symbol : | Rnf168 |
Synonyms : | RNF168; ring finger protein 168; E3 ubiquitin-protein ligase RNF168; ring fnger protein 168; 3110001H15Rik |
Gene ID : | 70238 |
mRNA Refseq : | NM_027355 |
Protein Refseq : | NP_081631 |
UniProt ID : | Q80XJ2 |
Products Types
◆ Recombinant Protein | ||
RNF168-4873H | Recombinant Human RNF168 protein(1-571aa), His-tagged | +Inquiry |
RNF168-679H | Recombinant Human RNF168 Protein, MYC/DDK-tagged | +Inquiry |
RNF168-30H | Recombinant Human RNF168, GST-tagged | +Inquiry |
Rnf168-5127M | Recombinant Mouse Rnf168 Protein (Asn423-Arg565), N-His tagged | +Inquiry |
RNF168-2338H | Recombinant Human RNF168, GST-tagged | +Inquiry |
◆ Lysates | ||
RNF168-1520HCL | Recombinant Human RNF168 cell lysate | +Inquiry |
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Not For Human Consumption!
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Customer Reviews (3)
Write a reviewNot only does it provide reliable and consistent results due to its high quality and purity, but it also holds significant value in understanding cellular processes and disease mechanisms.
This commitment to excellence ensures that researchers are provided with the most advanced and reliable tools for their investigations.
the RNF168 protein offers numerous advantages in trials and research experiments.
Q&As (5)
Ask a questionClinical trials investigating the potential use of RNF168 as a target for cancer therapy or as a biomarker for cancer prognosis may be underway, but specific details would need to be checked.
RNF168 plays a role in initiating a signaling cascade that leads to the recruitment of other DNA repair proteins to the site of DNA damage, promoting repair and maintaining genomic stability.
RNF168 interacts with various proteins involved in the DNA damage response, such as 53BP1 and BRCA1, to coordinate the repair of DNA lesions and maintain genomic stability.
Yes, inherited mutations in the RNF168 gene can increase the risk of developing certain cancers, particularly those associated with DNA damage and repair deficiencies.
The potential side effects and toxicities of targeting RNF168 in cancer therapy are still being explored, and would depend on the specific approach and modality used.
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