PEX3 Antikörper

Produktnummer ABIN7263371

Produktdetails anti-PEX3 Antikörper

Target: PEX3 (Peroxisomal Biogenesis Factor 3 (PEX3))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX3 Antikörper ist unkonjugiert

Applikation: Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human PEX3 (NP_003621.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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 PEX3

Target: PEX3 (Peroxisomal Biogenesis Factor 3 (PEX3))

Andere Bezeichnung: PEX3 (PEX3 Produkte)

Synonyme: DDBDRAFT_0204086 antikoerper, DDBDRAFT_0238047 antikoerper, DDB_0204086 antikoerper, DDB_0238047 antikoerper, zgc:56313 antikoerper, PBD10A antikoerper, TRG18 antikoerper, Peroxin-3 antikoerper, 1700014F15Rik antikoerper, 2810027F19Rik antikoerper, 2900010N04Rik antikoerper, peroxisomal biogenesis factor 3 antikoerper, peroxin 3 antikoerper, peroxisomal biogenesis factor 3 L homeolog antikoerper, LOC692959 antikoerper, CpipJ_CPIJ013204 antikoerper, pex3 antikoerper, PEX3 antikoerper, pex3.L antikoerper, Pex3 antikoerper

Hintergrund: The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. 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 Zellweger syndrome (ZWS).

Gen-ID: 8504

UniProt: P56589