Human TREX1 protein (Recombinant) (N-His-SUMO) (STJP008872)
SPECIFICATIONS
HostE.coli
ImmunogenHomo sapiens (Human)
General Information
| Short Description | Recombinant-Human TREX1-N-His-SUMO protein was developed from e.coli for the region N-His-SUMO. For use in research applications. |
| Applications | ELISA/Immunogen/SDS-PAGE/WB |
| Host | E.coli |
| Note | STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS. |
Product Properties
| Dilution Range | Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details. |
| Formulation | Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol. |
| Storage Instruction | Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at-20 to-80°C for twelve months from the date of receipt. |
Target Information
| Gene Symbol | TREX1 |
| Gene ID | 11277 |
| Uniprot ID | TREX1_HUMAN |
| Immunogen | Homo sapiens (Human) |
| Immunogen Region | Met11-His222 |
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 13'-5' Exonuclease Trex1Deoxyribonuclease IiiDnase Iii |
| Database Links | Reactome: R-HSA-3248023Reactome: R-HSA-3270619 |
| Cellular Localisation | NucleusCytoplasmCytosolEndoplasmic Reticulum MembranePeripheral Membrane ProteinRetained In The Cytoplasm Through The C-Terminal RegionLocalization To The Endoplasmic Reticulum Membrane Is Required To Direct Trex1 To Ruptured MicronucleiIn Response To Dna DamageTranslocates To The Nucleus Where It Is Specifically Recruited To Replication FociTranslocation To The Nucleus Also Occurs During Gzma-Mediated Cell Death |
| Alternative Protein Names | Three-Prime Repair Exonuclease 1 protein3'-5' Exonuclease Trex1 proteinDeoxyribonuclease Iii proteinDnase Iii proteinTREX1 protein |
Information sourced from Uniprot.org