PEX19 Antibody 1 Publications

Rabbit Polyclonal| Catalog number: 14713-1-AP

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Con: 20 μg/150 μl

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Species specificity:
human, mouse, rat, Arabidopsis thaliana

Positive WB detected in:
human heart tissue, multi-cells/tissue

Positive IP detected in:
K-562 cells

Positive IHC detected in:
human gliomas tissue

Recommended dilution:
WB : 1:500-1:1000
IP : 0.5-4.0 ug for IP and 1:200-1:1000 for WB
IHC : 1:50-1:500

Product Information


Purification method:
Antigen affinity purification


PBS with 0.02% sodium azide and 50% glycerol pH 7.3. Store at -20oC. Aliquoting is unnecessary for -20oC storage.

Immunogen Information

Full name:
peroxisomal biogenesis factor 19

Calculated molecular weight:
33 kDa

Observed molecular weight:
35-40 kDa

GenBank accession number:

Gene ID (NCBI):

Gene symbol

33 kDa housekeeping protein, D1S2223E, HK33, Peroxin 19, PEX19, PMP1, PMPI, PXF, PXMP1

Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. PEX19 gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs) (PMID: 14709540). PEX19 may bind newly synthesized PMPs and facilitate their insertion into the peroxisome membrane (PMID: 107044440. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14) (PMID:20683989) (PMID:10051604).

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