Date published: 2025-10-12

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TREX-2 Antibody (E-4): sc-390890

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Datasheets
  • TREX-2 Antibody (E-4) is a mouse monoclonal IgG1 κ TREX-2 antibody provided at 200 µg/ml
  • specific for an epitope mapping between amino acids 248-268 near the C-terminus of TREX-2 of human origin
  • TREX-2 Antibody (E-4) is recommended for detection of TREX-2 of mouse, rat and human origin by WB, IP, IF and ELISA
  • Anti-TREX-2 Antibody (E-4) is available conjugated to agarose for IP; HRP for WB, IHC(P) and ELISA; and to either phycoerythrin or FITC for IF, IHC(P) and FCM
  • also available conjugated to Alexa Fluor® 488, Alexa Fluor® 546, Alexa Fluor® 594 or Alexa Fluor® 647 for WB (RGB), IF, IHC(P) and FCM, and for use with RGB fluorescent imaging systems, such as iBright™ FL1000, FluorChem™, Typhoon, Azure and other comparable systems
  • also available conjugated to Alexa Fluor® 680 or Alexa Fluor® 790 for WB (NIR), IF and FCM; for use with Near-Infrared (NIR) detection systems, such as LI-COR®Odyssey®, iBright™ FL1000, FluorChem™, Typhoon, Azure and other comparable systems
  • m-IgG1 BP-HRP is the preferred secondary detection reagent for TREX-2 Antibody (E-4) for WB applications. This reagent is now offered in a bundle with TREX-2 Antibody (E-4) (see ordering information below).

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TREX-2 Antibody (E-4) is a mouse monoclonal IgG1 kappa light chain antibody that detects TREX-2 of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). TREX-2 (E-4) antibody is available in both non-conjugated and various conjugated forms, including agarose, horseradish peroxidase (HRP), phycoerythrin (PE), fluorescein isothiocyanate (FITC), and multiple Alexa Fluor® conjugates. TREX-2, also known as three prime repair exonuclease 2, is a crucial 279 amino acid enzyme that plays a significant role in maintaining genomic stability by participating in DNA repair processes. Located primarily in the nucleus, TREX-2 functions as an exonuclease, utilizing magnesium ions to catalyze the 3′ to 5′ exonucleolytic cleavage of mismatched double-stranded DNA, which is essential for correcting errors that may arise during DNA replication. This activity not only helps to eliminate mutant DNA but also generates nucleoside 5′ phosphates, thereby facilitating subsequent repair mechanisms. TREX-2 is expressed in various tissues, including the stomach, heart, breast, testis, prostate, colon, and skeletal muscle, and exists as a homodimer, which enhances enzymatic efficiency. Multiple isoforms of TREX-2 arise from alternative splicing, reflecting the complexity of regulation and function. The gene encoding human TREX-2 is located at Xq28 and is closely associated with the UCHL5IP gene, indicating potential co-regulation and functional interplay between these proteins.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

TREX-2 Antibody (E-4) References:

  1. Identification and expression of the TREX1 and TREX2 cDNA sequences encoding mammalian 3'-->5' exonucleases.  |  Mazur, DJ. and Perrino, FW. 1999. J Biol Chem. 274: 19655-60. PMID: 10391904
  2. Structure and expression of the TREX1 and TREX2 3' --> 5' exonuclease genes.  |  Mazur, DJ. and Perrino, FW. 2001. J Biol Chem. 276: 14718-27. PMID: 11278605
  3. The 3' 5' exonucleases.  |  Shevelev, IV. and Hübscher, U. 2002. Nat Rev Mol Cell Biol. 3: 364-76. PMID: 11988770
  4. The TREX2 3'-->5' exonuclease physically interacts with DNA polymerase delta and increases its accuracy.  |  Shevelev, IV., et al. 2002. ScientificWorldJournal. 2: 275-81. PMID: 12806015
  5. Sequence variants in the 3'-->5' deoxyribonuclease TREX2: identification in a genetic screen and effects on catalysis by the recombinant proteins.  |  Perrino, FW., et al. 2004. Adv Enzyme Regul. 44: 37-49. PMID: 15581481
  6. The human TREX2 3' -> 5'-exonuclease structure suggests a mechanism for efficient nonprocessive DNA catalysis.  |  Perrino, FW., et al. 2005. J Biol Chem. 280: 15212-8. PMID: 15661738
  7. Biochemical and cellular characteristics of the 3' -> 5' exonuclease TREX2.  |  Chen, MJ., et al. 2007. Nucleic Acids Res. 35: 2682-94. PMID: 17426129
  8. Cooperative DNA binding and communication across the dimer interface in the TREX2 3' --> 5'-exonuclease.  |  Perrino, FW., et al. 2008. J Biol Chem. 283: 21441-52. PMID: 18534978

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

TREX-2 Antibody (E-4)

sc-390890
200 µg/ml
$316.00

TREX-2 Antibody (E-4): m-IgG1 BP-HRP Bundle

sc-531745
200 µg Ab; 20 µg BP
$354.00

TREX-2 Antibody (E-4) AC

sc-390890 AC
500 µg/ml, 25% agarose
$416.00

TREX-2 Antibody (E-4) HRP

sc-390890 HRP
200 µg/ml
$316.00

TREX-2 Antibody (E-4) FITC

sc-390890 FITC
200 µg/ml
$330.00

TREX-2 Antibody (E-4) PE

sc-390890 PE
200 µg/ml
$343.00

TREX-2 Antibody (E-4) Alexa Fluor® 488

sc-390890 AF488
200 µg/ml
$357.00

TREX-2 Antibody (E-4) Alexa Fluor® 546

sc-390890 AF546
200 µg/ml
$357.00

TREX-2 Antibody (E-4) Alexa Fluor® 594

sc-390890 AF594
200 µg/ml
$357.00

TREX-2 Antibody (E-4) Alexa Fluor® 647

sc-390890 AF647
200 µg/ml
$357.00

TREX-2 Antibody (E-4) Alexa Fluor® 680

sc-390890 AF680
200 µg/ml
$357.00

TREX-2 Antibody (E-4) Alexa Fluor® 790

sc-390890 AF790
200 µg/ml
$357.00

TREX-2 (E-4) Neutralizing Peptide

sc-390890 P
100 µg/0.5 ml
$68.00

What application is the blocking peptide sc-390890 P appropriate for?

Asked by: Randy McDonald
Thank you for your question. The blocking peptide is intended for use as a negative control, by pre-adsorbing the mouse monoclonal antibody against the antigen. For full protocol details, please contact our Technical Services Department or view our online protocol here: https://www.scbt.com/scbt/resources/protocols/peptide-neutralization
Answered by: Technical Support
Date published: 2017-02-25
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Rated 4 out of 5 by from Works well for IPUsed this for IP of HCT 116 human colorectal carcinoma. Cells lysed in RIPA, 30 min @ 4 C rocking, then pelleted and sup collected/OD IP: Mixed 500 ug total lysate + 3 ug ab, end-over-end rocking 1 h @ 4 C Added 20 ul Protein A/G Bead slurry (sc-2003), rocked 2 h more @ 4 C (Collected / pelleted resin at 1,000 x g for 5 min for all washes) Washed 3 x 5 min in RIPA, then 1 x 5 min in PBS (both @ 4 C) Resuspended beads in equal volume 2x SDS loading dye (~15 ul) and boiled 5 min WB: TREX2 (E4) Ab 1:400 2 h @ RT anti-mouse IgG HRP 1:12,000 1 h @ RT Washed 3 x 10 min in TBS-T after each ab incubation Developed in ECL substrate 10 min before exposing to film. 1 min exposure shown below. Signal was robust so next time, I think I can easily decrease the amount of protein used for IP and/or increase the ab dilution to 1:500 or higher.
Date published: 2017-06-14
Rated 5 out of 5 by from Produced positive Western blot data of TREXProduced positive Western blot data of TREX-2 expression in CCRF-CEM and MOLT-4 nuclear extracts and mouse liver and human liver tissue extracts. -SCBT QC
Date published: 2013-06-12
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TREX-2 Antibody (E-4) is rated 4.5 out of 5 by 2.
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