Learn More
Description
Includes
Rabbit MaxPab™ affinity purified polyclonal anti-PEX19 (100μg); Mouse monoclonal anti-PEX19, IgG2aκ (20μg); Sufficient for at least 3-5 x 96 well plates using recommended protocols.
This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). 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 Zellweger syndrome (ZWS).
ELISA
Specifications
Specifications
| Antigen | PEX19 |
| Applications | ELISA |
| Classification | Monoclonal/Polyclonal |
| Conjugate | Unconjugated |
| Description | This antibody pair set comes with matched antibody pair to detect and quantify protein level of human PEX19. |
| Gene | PEX19 |
| Gene Alias | D1S2223E/HK33/PMP1/PMPI/PXF/PXMP1 |
| Gene Symbols | PEX19 |
| Host Species | Mouse, Rabbit |
| Purification Method | Affinity Purified |
| Show More |
By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.