PEX19 anticorps (AA 1-269)

N° du produit ABIN1885873

Cet anticorps Lapin Polyclonal détecte spécifiquement PEX19 dans WB, IHC et IF. Il présente une réactivité envers Humain.

Aperçu rapide pour PEX19 anticorps (AA 1-269) (ABIN1885873)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX19 est non-conjugé

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

Détail du produit anti-PEX19 anticorps

Épitope: AA 1-269

Purification: Purified by antigen-affinity chromatography.

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

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.100-1.500
Immunofluorescence: 1.100-1.200

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

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

Détails sur PEX19

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

Autre désignation: PEX19

Sujet: 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]

Poids moléculaire: 33 kDa

ID gène: 5824

NCBI Accession: NP_002848, NM_002857