Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody
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935106861
info@markelab.com
Precio
292.5€ (80 µl)
Antibody anti-WBSCR22
proveedor
Abbexareference
abx031474Tested Applications
ELISA, WBreactivity
Humanstatus
RUOclonality
PolyclonalDescripción
This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
Características del producto
category
Primary Antibodies
clonality
Polyclonal
reactivity
Human
immunogen target
Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22)
host
Rabbit
isotype
IgG
conjugation
Unconjugated
form
Liquid
tested applications
ELISA, WB
purification
Purified through a protein A column, followed by peptide affinity purification.
recommended dilution
WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
buffer
PBS containing 0.09% sodium azide.
size 1
80 µl
size 2
400 µl
storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
or code
WBSCR22
dry ice
No
availability
Shipped within 5-10 working days.
uniprot id
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proveedor
Abbexareference
abx031474Tested Applications
ELISA, WBreactivity
Humanstatus
RUOclonality
PolyclonalThis gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typica...
292.5€ (80 µl)
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