PMP70 anticorps (C-Term)

N° du produit ABIN3030056

L’anticorps Lapin Polyclonal anti-PMP70 a été validé pour WB et IHC (p). Il convient pour détecter PMP70 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour PMP70 anticorps (C-Term) (ABIN3030056)

Antigène: PMP70 (ABCD3) (ATP-Binding Cassette, Sub-Family D (Ald), Member 3 (ABCD3))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PMP70 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-PMP70 anticorps

Épitope: C-Term

Purification: Antigen affinity

Immunogène: An amino acid sequence from the C-terminus of human PMP70 (EFKQITEDTVEFGS) was used as the immunogen for this PMP70 antibody.

Isotype: IgG

Information d'application

Indications d'application: The stated application concentrations are suggested starting amounts. Titration of the PMP70 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 0.5-1 μg/mL,IHC (Paraffin): 0.5-1 μg/mL

Restrictions: For Research Use only

Stockage

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: -20 °C

Stockage commentaire: After reconstitution, the PMP70 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Détails sur PMP70

Antigène: PMP70 (ABCD3) (ATP-Binding Cassette, Sub-Family D (Ald), Member 3 (ABCD3))

Autre désignation: PMP70

Sujet: 70 kDa peroxisomal membrane protein (PMP70), also called ATP-binding cassette sub-family D member 3, is a protein that in humans is encoded by the ABCD3 gene. The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. The gene was assigned to human chromosome 1p21-p22 by in situ hybridization. This peroxisomal membrane protein likely plays an important role in peroxisome biogenesis. Mutations have been associated with some forms of Zellweger syndrome, a heterogeneous group of peroxisome assembly disorders.

UniProt: P28288

Pathways: Monocarboxylic Acid Catabolic Process