PEX19 Products

Antibodies
PEX19 Antibody
PEX19 Antibody
Species: Hu, Mu, Rt, Bv
Applications: WB, ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
PEX19 Antibody
PEX19 Antibody
NBP1-92255
Species: Hu, Mu, Rt
Applications: WB, IHC, IHC-P
Host: Rabbit Polyclonal
PEX19 Antibody
PEX19 Antibody
H00005824-D01P
Species: Hu, Mu, Rt
Applications: WB
Host: Rabbit Polyclonal
Antibody Pairs
PEX19 Antibody Pair
PEX19 Antibody Pair
H00005824-AP11
Species: Hu
Applications: S-ELISA
PEX19 Antibody Pair
PEX19 Antibody Pair
H00005824-AP21
Species: Hu
Applications: S-ELISA
Lysates
PEX19 Overexpression Lysate ( ...
PEX19 Overexpression Lysate (Native)
NBL1-14301
Applications: WB
PEX19 Overexpression Lysate ( ...
PEX19 Overexpression Lysate (Denat...
H00005824-T01
Species: Hu
Applications: WB
Proteins
PEX19 Recombinant Protein Ant ...
PEX19 Recombinant Protein Antigen
NBP2-55465PEP
Species: Hu
Applications: B/N, Ctrl
PEX19 Recombinant Protein Ant ...
PEX19 Recombinant Protein Antigen
NBP1-92255PEP
Species: Hu
Applications: AC
Recombinant Human PEX19 Prote ...
Recombinant Human PEX19 Protein
NBP1-72444
Species: Hu
Applications: PAGE

Description

PEX19 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). [provided by RefSeq]

Bioinformatics

Uniprot Human
Human
Human
Human
Human
Human
Human
Mouse
Product By Gene ID 5824
Alternate Names
  • PMPI
  • Peroxin-19
  • PMP1
  • PXFperoxin-19
  • D1S2223Ehousekeeping gene, 33kD
  • Peroxisomal farnesylated proteinFLJ55296
  • HK3333 kDa housekeeping protein
  • PXMP1
  • peroxisomal biogenesis factor 19

PTMs for PEX19

Learn more about PTMs related to PEX19.

Farnesylation
Prenylation
Demethylation

Bioinformatics Tool for PEX19

Discover related pathways, diseases and genes to PEX19. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.
 
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