Price range: $268.00 through $328.00
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. [provided by RefSeq, Mar 2016],
| Size | 50μL/100μL |
| Target | ABHD11 |
| Reactivity | Human, Mouse |
| Applications | WB, ELISA |
| MW(Calculated) | |
| MW(Observed) | 32kD |
| Host Species | Rabbit |
| Isotype | IgG |
| Conjugate/Modification | Unmodified |
| Recommended Dilution Ratio | WB 1:500-1:2000; ELISA 1:20000; Not yet tested in other applications. |
| Formulation | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
| Purification | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
| Storage | -15°C to -25°C/1 year(Do not lower than -25°C) |
| Concentration | 1 mg/ml |
| Clonality | Polyclonal |
| Clone Number | |
| Immunogen | The antiserum was produced against synthesized peptide derived from human ABHD11. AA range:161-210 |
| Specificity | ABHD11 Polyclonal Antibody detects endogenous levels of ABHD11 protein. |
| Gene Name | ABHD11 |
| Protein Name | Abhydrolase domain-containing protein 11 |
| Other Name | ABHD11; / WBSCR21; / PP1226; / Abhydrolase domain-containing protein 11; / Williams-Beuren syndrome chromosomal region 21 protein |
| Species | Human |
| Gene ID | 83451 |
| Uniprot | Q8NFV4, |
| Species.1 | Mouse |
| Gene ID.1 | |
| Uniprot.1 | Q8K4F5 |
| Species.2 | |
| Gene ID.2 | |
| Uniprot.2 | |
| Cellular Localization | mitochondrion, |
| Tissue Expression | Ubiquitously expressed. |
| Signaling_pathway | |
| Research Areas | |
| Function | Caution:It is uncertain whether Met-1 or Met-10 is the initiator.,sequence Caution:Wrong choice of frame.,similarity:Belongs to the AB hydrolase superfamily.,tissue specificity:Ubiquitously expressed., |
