Mouse Alanine--TRNA Ligase, Cytoplasmic (AARS1) Protein

Este producto es parte de AARS - Alanine-TRNA Ligase
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1079€ (100 µg)

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935106861
info@markelab.com
name
Mouse Alanine--TRNA Ligase, Cytoplasmic (AARS1) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx692477
tested applications
SDS-PAGE

Description

Mouse AARS Protein is a recombinant protein from Mouse produced in Baculovirus-Insect Cells. A DNA sequence encoding the mouse AARS (Q8BGQ7) (Met 1-Asn 968) was fused with a polyhistidine tag at the C-terminus.

Documents del producto

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Product specifications

Category
Proteins and Peptides
Immunogen Target
Alanine--TRNA Ligase, Cytoplasmic (AARS1)
Host
Insect
Origin
Mouse
Observed MW
Molecular Weight: 108.3 kDa
Sequence Fragment: Met1-Asn968
Tag: C-terminal His tag
Validity: The validity for this protein is 12 months.
Expression
Recombinant
Purity
> 88% (SDS-PAGE)
Size 1
100 µg
Form
 
Tested Applications
SDS-PAGE
Buffer
Lyophilized from sterile 20mM Tris, 500mM NaCl, pH 7.4, 10% glycerol.
Availability
Shipped within 5-15 working days.
Storage
Aliquot and store at -20°C or -80°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q8BGQ7
Alias
AARS1,AARS
Background
Protein AARS1
Status
RUO
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

Alanine-tRNA ligase, encoded by the genes AARS1 (cytoplasmic) and AARS2 (mitochondrial), is a member of the aminoacyl-tRNA synthetase (aaRS) family. These enzymes are crucial for protein synthesis, catalyzing the attachment of alanine to its corresponding tRNA (tRNA^Ala) in a process known as tRNA aminoacylation. This reaction is an essential step in the translation process, ensuring accurate incorporation of alanine into nascent polypeptides according to the genetic code.AARS1 functions in the cytoplasm and is involved in general protein synthesis and AARS2 operates in mitochondria, where it is critical for mitochondrial protein synthesis, essential for maintaining respiratory chain function.The genes encoding these enzymes are conserved across species, reflecting their indispensable role in cellular physiology. Mutations in these genes are associated with various diseases, including neurodegenerative disorders, mitochondrial dysfunction, and cancer. 

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