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WBSCR27 Rabbit anti-Human, Polyclonal, Invitrogen™

Rabbit Polyclonal Antibody

Supplier:  Thermo Scientific PA548112

Catalog No. PA548112


Description

Description

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]
TRUSTED_SUSTAINABILITY
Specifications

Specifications

WBSCR27
Polyclonal
PBS with 0.09% sodium azide
Q8N6F8
METTL27
KLH conjugated synthetic peptide between 5-34 amino acids from the N-terminal region of human WBSCR27.
400 μL
Primary
Human
Antibody
IgG
Immunohistochemistry (Paraffin), Western Blot
Unconjugated
METTL27
Williams-Beuren syndrome chromosomal region 27 protein, WBSCR27
Rabbit
Antigen affinity chromatography
RUO
155368
-20° C, Avoid Freeze/Thaw Cycles
Liquid
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