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PEX3 antibody

Anti-PEX3 antibody used in IHC (Paraffin sections) (IHC-P). GTX64847
Anti-PEX3 antibody used in IHC (Paraffin sections) (IHC-P). GTX64847
Anti-PEX3 antibody used in Western Blot (WB). GTX64847
Anti-PEX3 antibody used in IHC (Paraffin sections) (IHC-P). GTX64847

Cat. No. GTX64847

Host

 Rabbit

Clonality

 Polyclonal

Isotype

 IgG

Application

 WB, IHC-P

Reactivity

 Human, Mouse, Rat
Package
100 μl ($399)
See all PEX3 products

APPLICATION

Application Note

*Optimal dilutions/concentrations should be determined by the researcher.
Application Recommended Dilution
WB 1:500 - 1:2000
IHC-P 1:50 - 1:200
Not tested in other applications.

Calculated MW

42 kDa. ( Note )

PROPERTIES

Form

Liquid

Buffer

PBS, 50% Glycerol

Preservative

0.02% Sodium azide

Storage

Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.

Concentration

Batch dependent (Please refer to the vial label for the specific concentration.)

Antigen Species

Human

Immunogen

Recombinant fusion protein containing a sequence corresponding to amino acids 144-373 of human PEX3 (NP_003621.1).

Purification

Purified by affinity chromatography

Conjugation

Unconjugated

Note

For laboratory research use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.

Purchasers shall not, and agree not to enable third parties to, analyze, copy, reverse engineer or otherwise attempt to determine the structure or sequence of the product.

TARGET

Synonyms

peroxisomal biogenesis factor 3 , PBD10A , PBD10B , TRG18

Background

The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. 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, Oct 2008]

Database

Research Area

DATA IMAGES

Anti-PEX3 antibody used in IHC (Paraffin sections) (IHC-P). GTX64847

GTX64847 IHC-P Image

IHC-P analysis of mouse kidney tissue using GTX64847 PEX3 antibody.
Dilution : 1:100

Anti-PEX3 antibody used in IHC (Paraffin sections) (IHC-P). GTX64847

GTX64847 IHC-P Image

IHC-P analysis of human liver damage tissue using GTX64847 PEX3 antibody.
Dilution : 1:100

Anti-PEX3 antibody used in Western Blot (WB). GTX64847

GTX64847 WB Image

WB analysis of various sample lysates using GTX64847 PEX3 antibody. The signal was developed with ECL plus-Enhanced.
Dilution : 1:1000
Loading : 25μg per lane

Anti-PEX3 antibody used in IHC (Paraffin sections) (IHC-P). GTX64847

GTX64847 IHC-P Image

IHC-P analysis of rat kidney tissue using GTX64847 PEX3 antibody.
Dilution : 1:100

REFERENCE

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REVIEW

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SDS
PBS.pdf
Glycerol.pdf
Sodium Azide.pdf
Package List Price ($)
$ 399