PEX3 Antibody

ProSci
Product Code: PSI-22-885
Product Group: Primary Antibodies
Supplier: ProSci
CodeSizePrice
PSI-22-885-50uL50uL£433.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Host Type: Rabbit
Antibody Isotype: IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Shipping:
Blue Ice or RT
Storage:
Store at -20°C. Avoid freeze / thaw cycles.

Images

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Western blot analysis of extracts of various cell lines, using PEX3 antibody (22-885) at 1:1000 dilution._Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution._Lysates/proteins: 25ug per lane._Blocking buffer: 3% nonfat dry milk in TBST._Detection: ECL Enhanced Kit._Exposure time: 90s.
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Immunohistochemistry of paraffin-embedded human liver damage using PEX3 antibody (22-885) at dilution of 1:100 (40x lens).
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Immunohistochemistry of paraffin-embedded rat kidney using PEX3 antibody (22-885) at dilution of 1:100 (40x lens).
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Immunohistochemistry of paraffin-embedded mouse kidney using PEX3 antibody (22-885) at dilution of 1:100 (40x lens).

Western blot analysis of extracts of various cell lines, using PEX3 antibody (22-885) at 1:1000 dilution._Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution._Lysates/proteins: 25ug per lane._Blocking buffer: 3% nonfat dry milk in TBST._Detection: ECL Enhanced Kit._Exposure time: 90s.
Immunohistochemistry of paraffin-embedded human liver damage using PEX3 antibody (22-885) at dilution of 1:100 (40x lens).
Immunohistochemistry of paraffin-embedded rat kidney using PEX3 antibody (22-885) at dilution of 1:100 (40x lens).
Immunohistochemistry of paraffin-embedded mouse kidney using PEX3 antibody (22-885) at dilution of 1:100 (40x lens).

Further Information

Additional Names:
PEX3, TRG18, PBD10A
Application Note:
WB: 1:500 - 1:2000

IHC: 1:50 - 1:200
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).
Buffer:
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Concentration:
batch dependent
Conjugate:
Unconjugated
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.
Immunogen:
Recombinant fusion protein containing a sequence corresponding to amino acids 144-373 of human PEX3 (NP_003621.1).
NCBI Gene ID #:
8504
NCBI Official Name:
peroxisomal biogenesis factor 3
NCBI Official Symbol:
PEX3
NCBI Organism:
Homo sapiens
Physical State:
Liquid
PREDICTED MOLECULAR WEIGHT:
Observed: 37kDa
Purification:
Affinity purification
Research Area:
Signal Transduction
Swissprot #:
P56589
User NOte:
Optimal dilutions for each application to be determined by the researcher.