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PEX12, Goat, Polyclonal Antibody, Abnova™
Description
This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS). [provided by RefSeq
Specifications
Specifications
| Antigen | PEX12 |
| Applications | ELISA |
| Classification | Polyclonal |
| Concentration | 0.5 mg/mL |
| Conjugate | Unconjugated |
| Description | Goat polyclonal antibody raised against synthetic peptide of PEX12. |
| Dilution | ELISA (1:8000) The optimal working dilution should be determined by the end user. |
| Formulation | In 0.5mg/mL Tris saline, pH 7.3 (0.02% sodium azide, 0.5% BSA) |
| Gene | PEX12 |
| Gene Alias | PAF-3 |
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For Research Use Only
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