WBSCR22 polyclonal Antibody | BS8836

WBSCR22 polyclonal Antibody | BS8836 | Gentaur UK, US & Europe Distribution

Host: Rabbit

Reactivity: Human,Rat

Application: WB IHC IF

Application Range: WB: 1:500~1:2000 IHC: 1:50~1:200 IF: 1:50~1:200

Background: 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.

Storage & Stability: Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

Specificity: WBSCR22 polyclonal Antibody detects endogenous levels of WBSCR22 protein.

Molecular Weight: ~ 36kDa

Note: For research use only, not for use in diagnostic procedure.

Alternative Names: Probable 18S rRNA (guanine-N (7) ) -methyltransferase; Bud site selection protein 23 homolog; Metastasis-related methyltransferase 1; Williams-Beuren syndrome chromosomal region 22 protein; WBSCR22; MERM1; HUSSY-03; PP3381

Immunogen: Recombinant full length Human WBSCR22.

Conjugate: Unconjugated

Modification: Unmodification

Purification & Purity: The Antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE) .

Pathway: