ARSL (NM_000047) Human Recombinant Protein
Product Specifications
Background
Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome. [provided by RefSeq, Sep 2013]
Synonyms
ARSE; ASE; CDPX; CDPX1; CDPXR
Gene ID
415
UniProt
P51690
Accession Number mRNA
NM_000047
Chromosomal Location
Xp22.33
Expression System
HEK293T
Tag
C-Myc/DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Druggable Genome, Transmembrane
Molecular Weight
62.2 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
ARSL
Species
Human
Protein ID
NP_000038
Overview
Recombinant protein of human arylsulfatase E (chondrodysplasia punctata 1) (ARSE)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/415
Uniprot URL
https://www.uniprot.org/uniprot/P51690
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_000047
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_000038
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