DTD1 Protein (Myc-DYKDDDDK Tag)

Catalog No. ABIN2722784

Product Details

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

Protein Type: Recombinant

Origin: Human

Source: HEK-293 Cells

Purification tag / Conjugate: This DTD1 protein is labelled with Myc-DYKDDDDK Tag.

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

Characteristics:

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

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

Application Details

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

Comment:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Handling

Concentration: 50 μg/mL

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

Storage: -80 °C

Storage Comment: 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.

Target Details

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

Alternative Name: Histidyl-Trna Synthetase 2,hars2 (DTD1 Products)

Synonyms: 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

Background: 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.

Molecular Weight: 53.3 kDa

NCBI Accession: NP_036340