PMP70 Antikörper (C-Term)

Produktnummer ABIN3030056

Der Kaninchen Polyklonal anti-PMP70 Antikörper wird verwendet zum Nachweis von PMP70 in Proben von Human, Maus und Ratte. Er wurde validiert für WB, IF und IHC (p).

Kurzübersicht für PMP70 Antikörper (C-Term) (ABIN3030056)

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PMP70 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Produktdetails anti-PMP70 Antikörper

Bindungsspezifität: C-Term

Verwendungszweck: PMP70 Antibody / ABCD3

Sequenz: EFKQITEDTV EFGS

Aufreinigung: Antigen affinity

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: 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.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: After reconstitution, the PMP70 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Details zu PMP70

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

Andere Bezeichnung: PMP70

Hintergrund: 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