| No | Size | Price | Availability | |
| ARPF120-61 | 50ul | 1500.00 | In Stock |  |
| ARPF120-61 | 100ul | 2000.00 | In Stock | |
| Source: | Rabbit | Gene Id: | 83451/22829 |
| Isotype: | IgG | Swiss Prot: | Q8NFZ3/Q8NFZ3 |
| 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, Jul 2008] |
| Reactivity | Human, Mouse, Rat |
| Tested applications | WB |
| Clonality | Polyclonal Antibody |
| Calculated MW | 50-100 kDa |
| Recommended Dilutions |
WB 1:500-1:2000
|
| Immunogen | peptide from human Neuroligin |
| Storage | Store at -20°C or -80°C in PBS with 0.02% sodium azide and 50% glycerol. Avoid freeze/thaw cycles. |
| Synonym |
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