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+1-888.733.6849
+1-617.299.7367 (Int’l)
+1-617.299.7367 (Int’l)
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sales@neoscientific.com
+1-888.733.6849
+1-617.299.7367 (Int’l)
+1-888.733.6849
+1-617.299.7367 (Int’l)
| Reactivity | Human Rat |
| Tested applications | WB IHC IF |
| Recommended Dilution | WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:100 |
| Calculated MW | 32kDa |
| Observed MW | Refer to figures |
| Immunogen | Recombinant protein of human WBSCR22 |
| Storage Buffer | Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| Synonym | WBMT; MERM1; PP3381; HUSSY-3; HASJ4442; |
Western blot analysis of extracts of various cells, using WBSCR22 antibody.
Immunohistochemistry of paraffin-embedded rat spleen using WBSCR22 antibody at dilution of 1:100 (x40 lens).
Immunohistochemistry of paraffin-embedded human kidney using WBSCR22 antibody at dilution of 1:100 (x40 lens).
Immunofluorescence analysis of MCF7 cell using WBSCR22 antibody. Blue: DAPI for nuclear staining.
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.
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