SARS2 Protein (Myc-DYKDDDDK Tag)
This Recombinant SARS2 protein is produced in HEK-293 Cells.
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Catalog No. ABIN2731407
$1,112.40
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20 μg
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United States
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Quick Overview for SARS2 Protein (Myc-DYKDDDDK Tag) (ABIN2731407)
Target
See all SARS2 Proteins
SARS2
(seryl-tRNA Synthetase 2, Mitochondrial (SARS2))
Protein Type
Recombinant
Origin
Human
Source
HEK-293 Cells
Application
Antibody Production (AbP), Standard (STD)
Purity
> 80 % as determined by SDS-PAGE and Coomassie blue staining
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Purification tag / Conjugate
- This SARS2 protein is labelled with Myc-DYKDDDDK Tag.
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Characteristics
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- Recombinant human SARS2 / SerRSmt protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
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seryl-tRNA Synthetase 2, Mitochondrial (SARS2) (AA 1-518) protein (GST tag)
SARS2 Origin: Human Host: Wheat germ Recombinant WB, ELISA, AP, AA
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Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays -
Comment
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The tag is located at the C-terminal.
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Restrictions
- For Research Use only
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Concentration
- 50 μg/mL
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Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
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Storage
- -80 °C
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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.
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- SARS2 (seryl-tRNA Synthetase 2, Mitochondrial (SARS2))
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Alternative Name
- Sars2,serrsmt
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Background
- This gene encodes the mitochondrial seryl-tRNA synthethase precursor, a member of the class II tRNA synthetase family. The mature enzyme catalyzes the ligation of Serine to tRNA(Ser) and participates in the biosynthesis of selenocysteinyl-tRNA(sec) in mitochondria. The enzyme contains an N-terminal tRNA binding domain and a core catalytic domain. It functions in a homodimeric form, which is stabilized by tRNA binding. This gene is regulated by a bidirectional promoter that also controls the expression of mitochondrial ribosomal protein S12. Both genes are within the critical interval for the autosomal dominant deafness locus DFNA4 and might be linked to this disease. Multiple transcript variants encoding different isoforms have been identified for this gene.
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Molecular Weight
- 54.3 kDa
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NCBI Accession
- NP_060297
Target
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