Anti-Recombinant-TREX1 antibody [RM2K47] (STJA0025912)

SPECIFICATIONS
ClonalityMonoclonal
HostRabbit
ConjugationUnconjugated
IsotypeIgG
STJA0025912
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General Information

Short DescriptionRabbit monoclonal anti-Recombinant-Three-Prime Repair Exonuclease 1 for use in IF, IHC and WB in Human samples. Datasheet included with dilution recommendations, and related reagents.
ApplicationsIF/IHC/WB
HostRabbit
ReactivityHuman
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityMonoclonal
Clone IDRM2K47
IsotypeIgG
ConjugationUnconjugated
PurificationProtein A/G purified from cell culture supernatant
Dilution RangeIF: 1:50-1:200, IHC: 1:100-1:200, WB: 1:1000-1:2000
Formulation0.01M PBS, pH 7.4, 0.05% BSA, 50% Glycerol, 0.05% Sodium Azide
Storage InstructionSuitable for storage at +4°C between 1-2 weeks. For longer term store at-20°C for up to 12 months.

Target Information

Gene SymbolTREX1
Gene ID11277
Uniprot IDTREX1_HUMAN

Additional Info

Post Translational Modifications Ubiquitinated, but not targeted to proteasomal degradation. Ubiquitination may be important for interaction with UBQLN1.
Function Major cellular 3'-to-5' DNA exonuclease which digests single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA) with mismatched 3' termini. Prevents cell-intrinsic initiation of autoimmunity. Acts by metabolizing DNA fragments from endogenous retroelements, including L1, LTR and SINE elements. Plays a key role in degradation of DNA fragments at cytosolic micronuclei arising from genome instability: its association with the endoplasmic reticulum membrane directs TREX1 to ruptured micronuclei, leading to micronuclear DNA degradation. Micronuclear DNA degradation is required to limit CGAS activation and subsequent inflammation. Unless degraded, these DNA fragments accumulate in the cytosol and activate the cGAS-STING innate immune signaling, leading to the production of type I interferon. Prevents chronic ATM-dependent checkpoint activation, by processing ssDNA polynucleotide species arising from the processing of aberrant DNA replication intermediates. Inefficiently degrades oxidized DNA, such as that generated upon antimicrobial reactive oxygen production or upon absorption of UV light. During GZMA-mediated cell death, contributes to DNA damage in concert with NME1. NME1 nicks one strand of DNA and TREX1 removes bases from the free 3' end to enhance DNA damage and prevent DNA end reannealing and rapid repair.
Protein Name Three-Prime Repair Exonuclease 1
3'-5' Exonuclease Trex1
Deoxyribonuclease Iii
Dnase Iii
Database Links Reactome: R-HSA-3248023
Reactome: R-HSA-3270619
Cellular Localisation Nucleus
Cytoplasm
Cytosol
Endoplasmic Reticulum Membrane
Peripheral Membrane Protein
Retained In The Cytoplasm Through The C-Terminal Region
Localization To The Endoplasmic Reticulum Membrane Is Required To Direct Trex1 To Ruptured Micronuclei
In Response To Dna Damage
Translocates To The Nucleus Where It Is Specifically Recruited To Replication Foci
Translocation To The Nucleus Also Occurs During Gzma-Mediated Cell Death
Alternative Antibody Names Anti-Three-Prime Repair Exonuclease 1 antibody
Anti-3'-5' Exonuclease Trex1 antibody
Anti-Deoxyribonuclease Iii antibody
Anti-Dnase Iii antibody
Anti-TREX1 antibody

Information sourced from Uniprot.org

Citations

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