METTL27 (NM_152559) Human Recombinant Protein
Selected Variant
PH38640M5
Size: 20 µg
Product Specifications
Background
This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008]
Overview
Recombinant protein of human Williams Beuren syndrome chromosome region 27 (WBSCR27)
Synonyms
WBSCR27
Gene ID
155368
UniProt
Q8N6F8
Accession Number mRNA
NM_152559
Chromosomal Location
7q11.23
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
Molecular Weight
26.3 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
METTL27
Species
Human
Protein ID
NP_689772
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/155368
Uniprot URL
https://www.uniprot.org/uniprot/Q8N6F8
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_152559
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_689772
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