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Western blot analysis in Hela cell line lysates (35ug/lane).
Western blot analysis in Hela cell line lysates (35ug/lane).

PEX19 Antibody

CATALOG NUMBER: 57-701

Clonality:
Polyclonal
Tested Applications:
WB
Host Species:
Rabbit
Species Reactivity:
Human
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human
Homology:
Predicted species reactivity based on immunogen sequence: Bovine, Rat
Immunogen:
This PEX19 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 33-61 amino acids from the N-terminal region of human PEX19.
Conjugate:
Unconjugated
Tested Applications:
WB
Application Note:
For WB starting dilution is: 1:1000
Predicted Molecular Weight:
33 kDa
Purification:
This antibody is purified through a protein A column, followed by peptide affinity purification.
Clonality:
Polyclonal
Isotype:
Rabbit Ig
Physical State:
Liquid
Buffer:
Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration:
batch dependent
Storage Conditions:
Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Ncbi Official Symbol:
PEX19
Additional Names:
Peroxisomal biogenesis factor 19, 33 kDa housekeeping protein, Peroxin-19, Peroxisomal farnesylated protein, PEX19, HK33, PXF
Protein Accession Number:
P40855
Protein Gi Number:
729723
Ncbi Gene Id Number:
5824
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
This gene is necessary for early peroxisomal biogenesis.It acts both as a cytosolic chaperone and as an import receptor forperoxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteinsthat are essential for the assembly of functional peroxisomes. Theperoxisome biogenesis disorders (PBDs) are a group of geneticallyheterogeneous autosomal recessive, lethal diseases characterized bymultiple defects in peroxisome function. These disorders have atleast 14 complementation groups, with more than one phenotype beingobserved for some complementation groups. Although the clinicalfeatures of PBD patients vary, cells from all PBD patients exhibita defect in the import of one or more classes of peroxisomal matrixproteins into the organelle. Defects in this gene are a cause ofZellweger syndrome (ZWS), as well as peroxisome biogenesis disordercomplementation group 14 (PBD-CG14), which is also known asPBD-CGJ. Alternative splicing results in multiple transcriptvariants.
Background Reference 1:
Mohamed, S., et al. Am. J. Med. Genet.152A (9), 2318-2321 (2010) :
Background Reference 2:
Schmidt, F., et al. J. Biol. Chem. 285(33):25410-25417(2010)
Background Reference 3:
Schueller, N., et al. EMBO J. 29(15):2491-2500(2010)
Background Reference 4:
Liu, Y., et al.Psychiatr Res (2010) In press :

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.

CATALOG NUMBER:

57-701

List Size:
400 ul

List Price:

$495.00

Datasheet
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