PEX19 Monoclonal / Biotin / 533

Product Details
Supplier
Catalog #: NBP2-43757B (View supplier product page)
Size 100 μl
Price $429.00
Antigen PEX19
Clone 533
Host Mouse
Isotype IgG2b
Conjugate Biotin
Target Species Human, Rat
Applications WB
About PEX19 and Biotin
PEX19 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. [provided by RefSeq, Aug 2010]
Citations
Additional
Sources
Reviews & Ratings
Biotin Excitation and Emission Spectra