| No | Size | Price | Availability | |
| ARP114049-01 | 50ul | 1500.00 | In Stock |  |
| ARP114049-01 | 100ul | 2000.00 | In Stock | |
| Source: | Rabbit | Gene Id: | 114049 |
| Isotype: | IgG | Swiss Prot: | O43709 |
| purity: | Affinity purification |
| 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. |
| Reactivity | Human |
| Tested applications | WB IHC IF |
| Clonality | Polyclonal Antibody |
| Calculated MW | 32kDa |
| Recommended Dilutions |
WB 1:500 - 1:2000
IHC 1:50 - 1:200
IF 1:20 - 1:100
|
| Immunogen | A recombinant protein of human WBSCR22 |
| Storage | Store at -20oC (regular) or -80oC (long term). Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| Synonym | WBMT, MERM1, PP3381, HUSSY-3, HASJ4442 |
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