PEX12 Antikörper (AA 290-359)

Produktnummer ABIN7269246

Der Kaninchen Polyklonal anti-PEX12 Antikörper (ABIN7269246) detektiert spezifisch PEX12 in WB. Dieser Antikörper reagiert spezifisch mit Proben aus Human.

Kurzübersicht für PEX12 Antikörper (AA 290-359) (ABIN7269246)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX12 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-PEX12 Antikörper

Bindungsspezifität: AA 290-359

Verwendungszweck: PEX12 Rabbit pAb

Sequenz: YNSDSPLLPK MKTVCPLCRK TRVNDTVLAT SGYVFCYRCV FHYVRSHQAC PITGYPTEVQ HLIKLYSPEN

Kreuzreaktivität: Human

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 290-359 of human PEX12 (NP_000277.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu PEX12

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

Andere Bezeichnung: PEX12

Hintergrund: This gene belongs to the peroxin-12 family. 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 of Zellweger syndrome (ZWS).,PEX12,PAF-3,PBD3A,Signal Transduction,PEX12

Molekulargewicht: 40kDa

Gen-ID: 5193

UniProt: O00623