HARS2 (NM_012208) Human Mass Spec Standard

CAT#: PH304925

HARS2 MS Standard C13 and N15-labeled recombinant protein (NP_036340)



  View other "HARS2" proteins (3)

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CNY 19,520.00


货期*
4周

规格
    • 10 ug

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经常一起买 (2)
Transient overexpression lysate of histidyl-tRNA synthetase 2, mitochondrial (putative) (HARS2), nuclear gene encoding mitochondrial protein
    • 100 ug

CNY 3,080.00


HARS2 mouse monoclonal antibody, clone OTI6F9 (formerly 6F9)
    • 100 ul

CNY 1,999.00
CNY 2,700.00

Specifications

Product Data
Description HARS2 MS Standard C13 and N15-labeled recombinant protein (NP_036340)
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC204925
Predicted MW 56.9 kDa
Protein Sequence
Tag C-Myc/DDK
Purity > 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration >0.05 µg/µL as determined by microplate BCA method
Labeling Method Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine
Buffer 25 mM Tris-HCl, 100 mM glycine, pH 7.3
Reference Data
RefSeq NP_036340
RefSeq Size 2515
RefSeq ORF 1518
Synonyms HARSL; HARSR; HisRS; HO3; PRLTS2
Locus ID 23438
Cytogenetics 5q31.3
Summary 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. [provided by RefSeq, Jul 2013]
Protein Pathways Aminoacyl-tRNA biosynthesis
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