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Anticorps Polyclonal de lapin anti-PEX7

PEX7 Polyclonal Antibody for WB, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, rat, souris

Applications

WB, Indirect ELISA

Conjugaison

Non conjugué

N° de cat : 20614-1-PBS

Synonymes

Peroxin 7, Peroxin-7, PEX, PTS2 receptor, PTS2R

Galerie de données de validation

Filter:
  • Western Blot (WB) analysis of various lysates using PEX7 Polyclonal antibody (20614-1-AP)

    WB analysis using 20614-1-AP (same clone as 20614-1-PBS)

    HEK-293T cells lysate was subjected to SDS PAGE followed by western blot with 20614-1-AP (PEX7 antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 20614-1-PBS in a different storage buffer formulation.

Informations sur le produit

20614-1-PBS cible PEX7 dans les applications de WB, Indirect ELISA et montre une réactivité avec des échantillons Humain, rat, souris

Réactivité Humain, rat, souris
Hôte / Isotype Lapin / IgG
Clonalité Polyclonal
Type Anticorps
Immunogène PEX7 Protéine recombinante Ag14666
Nom complet peroxisomal biogenesis factor 7
Masse moléculaire calculée 323 aa, 36 kDa
Poids moléculaire observé42 kDa
Numéro d’acquisition GenBankBC006268
Symbole du gène PEX7
Identification du gène (NCBI) 5191
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par affinité contre l'antigène
Tampon de stockage PBS only
Conditions de stockageStore at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

PEX7, also known as peroxisomal targeting signal 2 (PTS2) receptor, is one member of peroxins (PEXs) which are proteins required for peroxisome assembly. PEX5 and PEX7 function as receptors that recognize PTS1- and PTS2- containing proteins, respectively. PEX7 plays an essential role in peroxisomal protein import by binding to the N-terminal PTS2-type peroxisomal targeting signal. PEX7 defects are associated with peroxisome biogenesis disorder complementation group 11 (PBD-CG11), rhizomelic chondrodysplasia punctata type 1 (RCDP1) and Refsum disease.

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