Mouse tissue transglutaminase

Mouse tissue transglutaminase

Catalog Number:
E001055270ZED
Mfr. No.:
T040
Price:
$762
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      • Overview
        • His6-rmTG2 is based on clone IRAKp961C066Q. It is N-terminally fused to a hexahistidine-tag resulting in the encoded N-terminal amino acid sequence MHHHHHHAEELLL…. His6-rmTG2 is produced in E. coli and purified by ion metal chelating chromatography to more than 95 % purity.

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          More Details

      • Properties
        • Name
          Tissue-type Transglutaminase, TG2, TGase 2, protein-glutamine-γ-glutamyltransferase
          Source
          E. coli
          Type
          Recombinant Proteins
          Purification
          > 95 % (visually by SDS-PAGE)
          Formulation
          The Transglutaminase is lyophilized from 50 mM NaH2PO4, 150 mM NaCl, pH 8. Sample contains maltodextrin.
          Storage
          Store working aliquots at ≤ - 20°C. Avoid repeated freezing and thawing. Delivery is possible at ambient temperature
          Note
          INTENDED FOR RESEARCH USE ONLY, NOT FOR USE IN HUMAN, THERAPEUTIC OR DIAGNOSTIC APPLICATIONS.
          Molecular Weight
          78 kDa
          Class
          Animal Transglutaminase 2
          Reconstitution
          Add the volume of H2O the protein is lyophilized from (see Certificate of Analysis) to the vial of lyophilized powder. Rotate vial gently until solid dissolves. After reconstitution the solution should be stored frozen in working aliquots. Keep cooled on ice for short term storage.
          Activity
          Add 10 mM Ca2+ to activate His6-rmTG2.
      • Applications
        • Application Description
          His6-rmTG2 catalyzes acyl transfer reactions from glutamine residues in proteins or peptides to primary amines, e. g. the formation of ε-(γ-glutamyl) lysine bonds between proteins by transferring the acyl group of a peptide-bound glutamine residue to the primary amino group of a peptide-bound lysine residue. His6-rmTG2 may also be used for immunoprecipitation.
      • Reference
        • Chrobok et al., PLoS One. 2018, 13:e0196433
          Shinde et al., J. Mol. Cell Cardiol. 2018, 117:36-48
          Schaertl et al., J. Biomol. Screen. 2010, 15:478-87
          Schulze-Krebs et al., Brain Res. 2015, 1631:22-33

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