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AB138411

Anti-Artemis (phospho S516) antibody

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(2 Publications)

Rabbit Polyclonal Artemis phospho S516 antibody. Suitable for WB and reacts with Human samples. Cited in 2 publications.

View Alternative Names

ARTEMIS, ASCID, SCIDA, SNM1C, DCLRE1C, Protein artemis, DNA cross-link repair 1C protein, Protein A-SCID, SNM1 homolog C, SNM1-like protein, hSNM1C

1 Images
Western blot - Anti-Artemis (phospho S516) antibody (AB138411)
  • WB

Unknown

Western blot - Anti-Artemis (phospho S516) antibody (AB138411)

All lanes:

Western blot - Anti-Artemis (phospho S516) antibody (ab138411) at 1/500 dilution

All lanes:

HepG2 cell extracts (treated with EGF at 200 ng/ml for 30 minutes) at 30 µg

Predicted band size: 78 kDa

false

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

WB

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

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Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Purification notes
ab138411 was affinity purified from rabbit antiserum by affinity chromatography using epitope specific phosphopeptide. The antibody against non phosphopeptide was removed by chromatography using non phosphopeptide corresponding to the phosphorylation.
Storage buffer
pH: 7.4 Preservative: 0.02% Sodium azide Constituents: PBS, 50% Glycerol (glycerin, glycerine), 0.88% Sodium chloride
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Artemis also known as DNA cross-link repair 1C (DCLRE1C) is a protein that plays an important role in DNA repair. It has a molecular mass of approximately 78 kDa. Artemis expresses mainly in cells of the immune system including lymphocytes and has been shown to contribute to maintaining genome stability. The protein acts as a nuclease which means it can cleave phosphodiester bonds within a nucleic acid chain allowing for the resolution of DNA double-strand breaks (DSBs).
Biological function summary

Artemis functions in the resolution of DNA double-strand breaks during processes such as V(D)J recombination and class switch recombination which are essential for the immune system's adaptive response. It forms a complex with DNA-dependent protein kinase catalytic subunit (DNA-PKcs) which is essential for its activation. The complex is necessary for the non-homologous end joining (NHEJ) pathway a major pathway to repair DSBs. The proper functioning of Artemis ensures the integrity and diversity of the antigen receptor repertoire.

Pathways

Artemis plays a critical role in the non-homologous end joining pathway. This pathway is one of the two main mechanisms for repairing double-strand breaks in DNA the other being homologous recombination. Artemis works in conjunction with other proteins such as Ku70/80 and DNA ligase IV in NHEJ. Additionally Artemis's role in V(D)J recombination links it with key immune processes affecting the diversity of antibodies and T-cell receptors important for effective immune responses.

Improper function or mutations in the Artemis protein can lead to severe combined immunodeficiency (SCID) a disorder characterized by a lack of functional immune response. Artemis mutations relate to increased sensitivity to ionizing radiation linking it with radiosensitivity disorders. It also interacts with the protein ATM (ataxia-telangiectasia mutated) which is similarly involved in DNA damage response highlighting a connection between Artemis dysfunction and increased susceptibility to genomic instability-related disorders.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Nuclease involved in DNA non-homologous end joining (NHEJ); required for double-strand break repair and V(D)J recombination (PubMed : 11336668, PubMed : 11955432, PubMed : 12055248, PubMed : 14744996, PubMed : 15071507, PubMed : 15574326, PubMed : 15936993). Required for V(D)J recombination, the process by which exons encoding the antigen-binding domains of immunoglobulins and T-cell receptor proteins are assembled from individual V, (D), and J gene segments (PubMed : 11336668, PubMed : 11955432, PubMed : 14744996). V(D)J recombination is initiated by the lymphoid specific RAG endonuclease complex, which generates site specific DNA double strand breaks (DSBs) (PubMed : 11336668, PubMed : 11955432, PubMed : 14744996). These DSBs present two types of DNA end structures : hairpin sealed coding ends and phosphorylated blunt signal ends (PubMed : 11336668, PubMed : 11955432, PubMed : 14744996). These ends are independently repaired by the non homologous end joining (NHEJ) pathway to form coding and signal joints respectively (PubMed : 11336668, PubMed : 11955432, PubMed : 14744996). This protein exhibits single-strand specific 5'-3' exonuclease activity in isolation and acquires endonucleolytic activity on 5' and 3' hairpins and overhangs when in a complex with PRKDC (PubMed : 11955432, PubMed : 15071507, PubMed : 15574326, PubMed : 15936993). The latter activity is required specifically for the resolution of closed hairpins prior to the formation of the coding joint (PubMed : 11955432). Also required for the repair of complex DSBs induced by ionizing radiation, which require substantial end-processing prior to religation by NHEJ (PubMed : 15456891, PubMed : 15468306, PubMed : 15574327, PubMed : 15811628).
See full target information DCLRE1C pS516

Publications (2)

Recent publications for all applications. Explore the full list and refine your search

Nucleic acids research 51:7972-7987 PubMed37395399

2023

DNA-PK is activated by SIRT2 deacetylation to promote DNA double-strand break repair by non-homologous end joining.

Applications

Unspecified application

Species

Unspecified reactive species

PamelaSara E Head,Priya Kapoor-Vazirani,Ganji P Nagaraju,Hui Zhang,Sandip K Rath,Nho C Luong,Ramona Haji-Seyed-Javadi,Fatmata Sesay,Shi-Ya Wang,Duc M Duong,Waaqo Daddacha,Elizabeth V Minten,Boying Song,Diana Danelia,Xu Liu,Shuyi Li,Eric A Ortlund,Nicholas T Seyfried,David M Smalley,Ya Wang,Xingming Deng,William S Dynan,Bassel El-Rayes,Anthony J Davis,David S Yu

Frontiers in pharmacology 11:580978 PubMed33628171

2021

An Integrated Strategy for Effective-Component Discovery of Astragali Radix in the Treatment of Lung Cancer.

Applications

Unspecified application

Species

Unspecified reactive species

Bing Yang,Nan Yang,Yaping Chen,Maomao Zhu,Yuanpei Lian,Zhiwei Xiong,Bei Wang,Liang Feng,Xiaobin Jia
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