PEX26 Antikörper (AA 1-265)

Produktnummer ABIN1885866

Dieses Anti-PEX26-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von PEX26 in WB, IHC und IF. Geeignet für Human.

Kurzübersicht für PEX26 Antikörper (AA 1-265) (ABIN1885866)

Target: PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX26 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Produktdetails anti-PEX26 Antikörper

Bindungsspezifität: AA 1-265

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 265 of Human PEX26

Anwendungsinformationen

Applikationshinweise: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.50-1.500
Immunofluorescence: 1.100-1.200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Konservierungsmittel: Thimerosal (Merthiolate)

Vorsichtsmaßnahmen: Biohazard Informations: This product contains thimerosal which is hazardous.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Details zu PEX26

Target: PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))

Andere Bezeichnung: Peroxin 26

Hintergrund: This gene belongs to the peroxin-26 gene family.It is probably required for protein import into peroxisomes.It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes.Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8).PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix.The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP).Two transcript variants encoding the same protein have been identified for this gene.[provided by RefSeq]

Molekulargewicht: 34 kDa

Gen-ID: 55670

NCBI Accession: NP_060399, NM_017929