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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]

Overview

Recombinant protein of human arylsulfatase E (chondrodysplasia punctata 1) (ARSE)

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

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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