Anti-WBSCR22 Polyclonal Antibody
Cat: K005168P
Summary:
| 【Product name】：Anti-WBSCR22 Polyclonal Antibody | 【Source】：Rabbit |
| 【Isotype】：IgG | |
| 【Gene ID】：114049 | 【Swiss Prot】：O43709 |
| 【Species reactivity】：Human,Rat | |
| 【Tested applications】：IF,WB | |
| 【Immunogen】：Recombinant protein of human WBSCR22 | |
| 【Storage】：Store at -20℃, avoid freeze/thaw cycles. | |
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.
Verified picture:
Immunofluorescence analysis of MCF7 cell using WBSCR22 antibody. Blue: DAPI for nuclear staining.
Western blot analysis with WBSCR22 antibody diluted at 1:1000;Lane: NCI-H460 A549.
Immunofluorescence analysis of A549 cells using WBSCR22 antibody diluted at 1:100.