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WBSCR27 Rabbit anti-Human, Polyclonal, Invitrogen™
Rabbit Polyclonal Antibody
Supplier: Thermo Scientific PA548112
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]
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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