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Recombinant Human Three-prime repair exonuclease 1 (TREX1)

The intact gene sequence of the human three-prime repair exonuclease 1 (TREX1) is expressed in the baculovirus. The resulting protein is fused with the MBP-tag at the N-terminus and the 6xHis-tag at the C-terminus, ultimately leading to the production of the recombinant human TREX1 (CSB-BP865133HU). Its purity is greater than 85% determined by SDS-PAGE. It migrated to the molecular weight band of approximately 65 kDa. The target protein TREX1 plays an important role in genomic DNA degradation, cell death processes, and gap-filling during DNA repair or proofreading during lagging-strand DNA synthesis.

ACP03209

The intact gene sequence of the human three-prime repair exonuclease 1 (TREX1) is expressed in the baculovirus. The resulting protein is fused with the MBP-tag at the N-terminus and the 6xHis-tag at the C-terminus, ultimately leading to the production of the recombinant human TREX1 (CSB-BP865133HU). Its purity is greater than 85% determined by SDS-PAGE. It migrated to the molecular weight band of approximately 65 kDa. The target protein TREX1 plays an important role in genomic DNA degradation, cell death processes, and gap-filling during DNA repair or proofreading during lagging-strand DNA synthesis.

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Specifications


Cat.No ACP03209 Target NameTREX1
Target SynonymsTREX1; Three-prime repair exonuclease 1; EC 3.1.11.2; 3'-5' exonuclease TREX1; Deoxyribonuclease III; DNase IIIFormLiquid or Lyophilized powder
Expression SystemBaculovirusExpression Range1-369aa
Mol Weight82.9 kDaProtein LengthFull length
PurityGreater than 85% as determined by SDS-PAGE.Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDQ9NSU2
Background Information
  • Uniprot Id

    Q9NSU2

  • Target Species

    Human

  • Target Name

    TREX1

  • Target Full Name

    Three-prime repair exonuclease 1

  • Target 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. Unless degraded, these DNA fragments accumulate in the cytosol and activate the IFN-stimulatory DNA (ISD) response and innate immune signaling. 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.

  • Target Involvement

    Aicardi-Goutieres syndrome 1 (AGS1); Systemic lupus erythematosus (SLE); Chilblain lupus 1 (CHBL1); Vasculopathy, retinal, with cerebral leukodystrophy (RVCL)

  • Target Subcellular Location

    Nucleus. Cytoplasm, cytosol. Endoplasmic reticulum membrane; Peripheral membrane protein.

  • Target Protein Families

    Exonuclease superfamily, TREX family

  • Target Tissue Specificity

    Detected in thymus, spleen, liver, brain, heart, small intestine and colon.

  • Target Research Area

    Epigenetics and Nuclear Signaling

  • Target Synonyms

    TREX1; Three-prime repair exonuclease 1; EC 3.1.11.2; 3'-5' exonuclease TREX1; Deoxyribonuclease III; DNase III

  • Target Background

    This gene encodes a nuclear protein with 3' exonuclease activity. The encoded protein may play a role in DNA repair and serve as a proofreading function for DNA polymerase. Mutations in this gene result in Aicardi-Goutieres syndrome, chilblain lupus, Cree encephalitis, and other diseases of the immune system. Alternative splicing results in multiple transcript variants.

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