PEX12 Antikörper (Middle Region)

Produktnummer ABIN954095

Der Kaninchen Polyklonal Anti-PEX12-Antikörper wurde für WB und EIA validiert. Er ist geeignet, PEX12 in Proben von Human und Maus zu detektieren.

Kurzübersicht für PEX12 Antikörper (Middle Region) (ABIN954095)

Target: PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX12 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Enzyme Immunoassay (EIA)

Produktdetails anti-PEX12 Antikörper

Bindungsspezifität: AA 137-167, Middle Region

Spezifität: This antibody recognizes Human and Mouse Peroxin 12 / PEX12 (Center).

Aufreinigung: Protein A column, followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 137~167 amino acids from the Central region of human PEX12

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu PEX12

Target: PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

Andere Bezeichnung: Peroxin 12 / PEX12

Hintergrund: 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.Synonyms: PAF-3, PAF3, Peroxin-12, Peroxisome assembly factor 3, Peroxisome assembly protein 12

Molekulargewicht: 40797 Da

Gen-ID: 5193

NCBI Accession: NP_000277