NSUN5 (NM_148956) Human Recombinant Protein
Product Specifications
Background
This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Synonyms
NOL1; NOL1R; NSUN5A; p120; p120 (NOL1) ; WBSCR20; WBSCR20A
Gene ID
55695
UniProt
Q96P11
Accession Number mRNA
NM_148956
Chromosomal Location
7q11.23
Expression System
E. coli
Tag
N-GST and 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
25mM Tris, pH8.0, 150mM NaCl, 10% glycerol, 1% Sarkosyl.
Molecular Weight
78.2 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
NSUN5
Species
Human
Protein ID
NP_683759
Overview
Purified recombinant protein of Human NOP2/Sun domain family, member 5 (NSUN5), transcript variant 1, full length, with N-terminal GST and C-terminal HIS tag, expressed in E. coli, 50ug
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/55695
Uniprot URL
https://www.uniprot.org/uniprot/Q96P11
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_148956
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_683759
Curated Selection
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