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Home Antibody All anti-PEX19 antibodies

Anti-PEX19 Antibody

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Specifications Citations Related Products Product Documents
SKU Description Amount Price Availability*  
TA307905
  • Rabbit Polyclonal antibody to PEX19 (peroxisomal biogenesis factor 19)
  • Free Sample of Positive Control: HEK293T cell transient overexpression lysate (LC427370) , 20ug Explanation
100ul 325 3-7 Days
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WB(3)
IHC(1)
IF(1)
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Also for PEX19 (NM_001131039)
cDNA Clone shRNA/siRNA Lysate Protein Antibody

OriGene Data

ImmunogenRecombinant fragment corresponding to a region within amino acids 1 and 299 of PEX19 (Uniprot ID#P40855)
Clone Name IsotypeIgG
Species ReactivityHuman, Mouse Concentration1mg/ml
Guaranteed Application *WB, IHC, IF Suggested DilutionsICC/IF:1:100-1:1000; IHC:1:100-1:1000; WB:1:1000-1:10000
Predicted MW Explanation 33kDa
Buffer0.1M Tris, 0.1M Glycine, 10% Glycerol (pH7). 0.01% Thimerosal was added as a preservative.
Purification Purified by antigen-affinity chromatography.

Reference Data

Target NameHomo sapiens peroxisomal biogenesis factor 19 (PEX19), transcript variant 2
Alternative NameD1S2223E; FLJ55296; HK33; PMP1; PMPI; PXF; PXMP1; HK33; PMP1; PMPI; PXF; PXMP1; OTTHUMP00000031848; housekeeping gene, 33kD; peroxisomal farnesylated protein; peroxisomal biogenesis factor 19
Database LinkNP_001124511
Entrez Gene 5824 Human
Entrez Gene 19298 Mouse
FunctionThis 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. 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]
Related PathwayDruggable Genome

* Availability is in business days
* OriGene provides validated application data and protocol, with money back guarantee.

WB Image
Sample (30 ug of whole cell lysate). A: Raji. B: K562. C: THP-1. D: NCI-H929. 12% SDS PAGE. TA307905 diluted at 1:10000.
WB Image
Sample (50 ug of whole cell lysate). A: mouse liver. 12% SDS PAGE. TA307905 diluted at 1:10000.
WB Image
PEX19 antibody detects PEX19 protein by Western blot analysis. A. 30 ug PC-12 whole cell lysate/extract. B. 30 ug Rat-2 whole cell lysate/extract. 10 % SDS-PAGE. PEX19 antibody (TA307905) dilution: 1:1000
IHC Image
Immunohistochemical analysis of paraffin-embedded SW480 xenograft, using PEX19(TA307905) antibody at 1:500 dilution.
IF Image
Confocal immunofluorescence analysis (Olympus FV10i) of methanol-fixed HeLa, using PEX19(TA307905) antibody (Green) at 1:500 dilution. Alpha-tubulin filaments were labeled with anti-alpha tubulin antibody (Red) at 1:2000.

 

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