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.
Immunogen Information
Immunogen
Recombinant fusion protein of human WBSCR27 (NP_689772.2).
Gene ID
155368
Swissprot
Q8N6F8
Synonyms
METTL27WBSCR27
Calculated MW
26 kDa
Observed MW
26 kDa
Applications
Reactivity
Human,Mouse,Rat
Tested Applications
WB
Conjugation
Unconjugated
Dilution
WB 1:500-1:2000
Concentration
1 mg/mL
Storage Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Storage Instructions
Store at -20°C. Avoid freeze / thaw cycles.
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