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PEX19 Antibody (9O7Q9)

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Western Blot: PEX19 Antibody (9O7Q9) [NBP3-15701] - Western blot analysis of extracts of various cell lines, using PEX19 antibody (NBP3-15701) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at ...read more

Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB
Clone
9O7Q9
Clonality
Monoclonal
Host
Rabbit
Conjugate
Unconjugated

Order Details

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PEX19 Antibody (9O7Q9) Summary

Additional Information
Recombinant Monoclonal Antibody
Immunogen
A synthetic peptide corresponding to a sequence within amino acids 1-100 of human PEX19 (P40855). MAAAEEGCSVGAEADRELEELLESALDDFDKAKPSPAPPSTTTAPDASGPQKRSPGDTAKDALFASQEKFFQELFDSELASQATAEFEKAMKELAEEEPH
Isotype
IgG
Clonality
Monoclonal
Host
Rabbit
Gene
PEX19
Purity
Affinity purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Western Blot 1:500 - 1:1000

Packaging, Storage & Formulations

Storage
Store at -20C. Avoid freeze-thaw cycles.
Buffer
PBS, 0.05% BSA, 50% glycerol, pH7.3
Preservative
0.02% Sodium Azide
Purity
Affinity purified

Alternate Names for PEX19 Antibody (9O7Q9)

  • D1S2223Ehousekeeping gene, 33kD
  • HK3333 kDa housekeeping protein
  • Peroxin-19
  • peroxisomal biogenesis factor 19
  • Peroxisomal farnesylated proteinFLJ55296
  • PMP1
  • PMPI
  • PXFperoxin-19
  • PXMP1

Background

PEX19 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]

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Product General Protocols

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Video Protocols

WB Video Protocol

FAQs for PEX19 Antibody (NBP3-15701) (0)

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Secondary Antibodies

 

Isotype Controls

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Bioinformatics

Gene Symbol PEX19