DTD1 Protein (Myc-DYKDDDDK Tag)

Produktnummer ABIN2722784

Produktdetails

Target: DTD1 (D-Tyrosyl-tRNA Deacylase 1 Homolog (S. Cerevisiae) (DTD1))

Protein-Typ: Recombinant

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses DTD1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human Histidyl-tRNA synthetase 2 / HARS2 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: DTD1 (D-Tyrosyl-tRNA Deacylase 1 Homolog (S. Cerevisiae) (DTD1))

Andere Bezeichnung: Histidyl-Trna Synthetase 2,hars2 (DTD1 Produkte)

Synonyme: 0610006H08Rik Protein, Hars2 Protein, C20orf88 Protein, DUEB Protein, HARS2 Protein, bA379J5.3 Protein, bA555E18.1 Protein, pqn-68 Protein, hars2 Protein, zgc:92657 Protein, D-tyrosyl-tRNA deacylase 1 Protein, Dtd1 Protein, DTD1 Protein, dtd1 Protein

Hintergrund: Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is an enzyme belonging to the class II family of aminoacyl-tRNA synthetases. Functioning in the synthesis of histidyl-transfer RNA, the enzyme plays an accessory role in the regulation of protein biosynthesis. The gene is located in a head-to-head orientation with HARS on chromosome five, where the homologous genes likely share a bidirectional promoter. Mutations in this gene are associated with the pathogenesis of Perrault syndrome, which involves ovarian dysgenesis and sensorineural hearing loss. Alternative splicing results in multiple transcript variants of this gene.

Molekulargewicht: 53.3 kDa

NCBI Accession: NP_036340