| No | Size | Price | Availability | |
| ARP83451-61 | 50ul | 1500.00 | In Stock |  |
| ARP83451-61 | 100ul | 2000.00 | In Stock | |
| Source: | Rabbit | Gene Id: | 83451 |
| Isotype: | IgG | Swiss Prot: | Q8NFV4 |
| purity: | Affinity purification |
| Background: |
| This gene encodes a protein containing an alpha/beta hydrolase fold domain. 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 described, but their biological validity has not been determined. [provided by RefSeq |
| Reactivity | Human |
| Tested applications | WB |
| Clonality | Polyclonal Antibody |
| Calculated MW | 32 kDa |
| Recommended Dilutions |
WB 1:500-1:1000
|
| Immunogen | A synthetic peptide |
| Storage | Store at -20°C or -80°C in PBS with 0.02% sodium azide and 50% glycerol. Avoid freeze/thaw cycles. |
| Synonym | ABHDB, abhydrolase domain containing 11, EC 3.-.-.-, PP1226, WBSCR21, Williams-Beuren syndrome chromosomal region 21 protein |
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