ET7110-89
Scientist.com Supplier
Anti-PEX19 Antibody [JE54-93]
HuaBio
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DESCRIPTION
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. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some 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), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants.
DETAILS
- Host: Rabbit
- Type: Primary
- Uniprot: SwissProt: P40855 Human
- Clone Id: JE54-93
- Clonality: Recombinant Rabbit monoclonal Antibody
- Conjugate: Non-conjugated
- Alias Names: 33 kDa housekeeping protein antibody D1S2223E antibody HK33 antibody Housekeeping gene 33kD antibody OK/SW-cl.22 antibody PBD12A antibody Peroxin 19 antibody Peroxin-19 antibody Peroxisomal biogenesis factor 19 antibody Peroxisomal farnesylated protein antibody PEX19 antibody PEX19_HUMAN antibody PMP1 antibody PMPI antibody PXF antibody PXMP1 antibody
- Application: WB,IHC-P,FC
- Epitope Region: Recombinant protein within Human PEX19 aa 1-140 / 299.
- Protein Target: PEX19
- Target Species: Human
- Species Reactivity: Human