AMELX (NM_182681) Human Recombinant Protein
Product Specifications
Background
This gene encodes a member of the amelogenin family of extracellular matrix proteins. Amelogenins are involved in biomineralization during tooth enamel development. Mutations in this gene cause X-linked amelogenesis imperfecta. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Synonyms
AI1E; AIH1; ALGN; AMG; AMGL; AMGX
Gene ID
265
UniProt
Q99217
Accession Number mRNA
NM_182681
Chromosomal Location
Xp22.2
Expression System
HEK293
Tag
C-HIS
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
300 mM imidazole, PBS, pH7.4, 10% glycerol
Function
Druggable Genome, Secreted Protein, Transmembrane
Molecular Weight
19.4kDa
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
AMELX
Species
Human
Protein ID
NP_872622
Overview
Purified recombinant protein of Human amelogenin, X-linked (AMELX), Met17-End, with C-terminal His tag, secretory expressed in HEK293 cells, 50ug
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/265
Uniprot URL
https://www.uniprot.org/uniprot/Q99217
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_182681
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_872622
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