GeneTex
United States (US)

PEX3 antibody

GTX64847_20180530_IHC-P_2_18121411_297.jpg
GTX64847_20180530_IHC-P_18121411_652.jpg
GTX64847_20180530_IHC-P_1_18121411_635.jpg
GTX64847_20180530_WB_18121411_398.jpg

Cat No. GTX64847

Host Rabbit
Clonality Polyclonal
Isotype IgG
Application WB, IHC-P
Reactivity Human, Mouse, Rat
APPLICATION

Application Note

*Optimal dilutions/concentrations should be determined by the researcher.
Application 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 pH7.3, 0.02% sodium azide, 50% glycerol.

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.

Antigen Species

Human

Immunogen

Recombinant funsion 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 In vitro laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.
TARGET

Synonyms

TRG18 Antibody , PBD10A Antibody

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

DATA IMAGES
GTX64847_20180530_IHC-P_2_18121411_297.jpg

GTX64847 IHC-P Image

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

GTX64847_20180530_IHC-P_18121411_652.jpg

GTX64847 IHC-P Image

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

GTX64847_20180530_IHC-P_1_18121411_635.jpg

GTX64847 IHC-P Image

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

GTX64847_20180530_WB_18121411_398.jpg

GTX64847 WB Image

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

Package List Price ($)
$ 319