PEX19 antibody (AA 1-269)

Catalog No. ABIN1885873

This Rabbit Polyclonal antibody specifically detects PEX19 in WB, IHC and IF. It exhibits reactivity toward Human.

Quick Overview for PEX19 antibody (AA 1-269) (ABIN1885873)

Target: PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX19 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Product Details anti-PEX19 Antibody

Binding Specificity: AA 1-269

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 269 of PEX19

Application Details

Application Notes: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.100-1.500
Immunofluorescence: 1.100-1.200

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Preservative: Thimerosal (Merthiolate)

Precaution of Use: Biohazard Informations: This product contains thimerosal which is hazardous.

Storage: 4 °C/-20 °C

Storage Comment: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Target Details for PEX19

Target: PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

Alternative Name: PEX19

Background: This gene 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]

Molecular Weight: 33 kDa

Gene ID: 5824

NCBI Accession: NP_002848, NM_002857