Product Description
WBSCR22 polyclonal antibody is available at gentaur for next week delivery
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.
Applications: WB IHC IF
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).
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.
W4BiowMW: ~ 36kDa
Reactivity: Human,Rat
Note: For research use only, not for use in diagnostic procedure.
Immunogen:
Recombinant full length Human WBSCR22.Alternative Name:
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; PP3381Western blot analysis: Immunofluorescence analysis of MCF7 cell using WBSCR22 antibody. Blue: DAPI for nuclear staining.
Immunohistochemistry: Western blot analysis of extracts of various cell lines, using WBSCR22 antibody.
Immunofluorescence analysis:
Host: Rabbit
Swiss-Prot: O43709
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