PEX19 Polyclonal Antibody

CAT: 0866-RD83330A-01Size: 60 μLDry Ice: NoHazardous: No
CAT#:0866-RD83330A-01Size:60 μL
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Background
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.
Description
This is a PEX19 Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.
Synonyms
PEX19, D1S2223E, HK33, PBD12A, PMP1, PMPI, PXF, PXMP1
Gene ID
5824
Swiss Prot
P40855
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein of human PEX19 (NP_002848.1) .
Conjugation
Unconjugated
Type
Polyclonal Antibody
Applications
IF
Purification Method
Affinity purification
Assay Type
Antibody
Concentration
1 mg/mL
Dilution
IF 1:50-1:200
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Storage Conditions
Store at -20°C. Avoid freeze / thaw cycles.
Host or Source
Rabbit
Isotype
IgG

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