Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody

Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody

Pida mas información

935106861

info@markelab.com

Precio

195€ (20 µl)

Antibody anti-WBSCR22

proveedor

Abbexa

reference

abx005524

Tested Applications

ELISA, WB, IF/ICC

reactivity

Human, Rat

status

RUO

clonality

Polyclonal

Descripción

WBSCR22 Antibody is a Rabbit Polyclonal antibody against WBSCR22. 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. Alternatively spliced transcript variants have been found.

Características del producto

category

Primary Antibodies


clonality

Polyclonal


reactivity

Human, Rat


immunogen target

Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22)


host

Rabbit


isotype

IgG


conjugation

Unconjugated


form

Liquid


tested applications

ELISA, WB, IF/ICC


purification

Purified by affinity chromatography.


recommended dilution

ELISA: 1 µg/ml, WB: 1/500 - 1/2000, IF/ICC: 1/50 - 1/100. Optimal dilutions/concentrations should be determined by the end user.


buffer

PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol.


size 1

20 µl


size 2

100 µl


size 3

2 × 100 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.


NCBI accession

NP_059998.2


note

Concentration: > 0.2 mg/ml -


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