PEX13 Antikörper (AA 342-403)

Produktnummer ABIN1886384

Produktdetails anti-PEX13 Antikörper

Target: PEX13 (Peroxisomal Biogenesis Factor 13 (PEX13))

Bindungsspezifität: AA 342-403

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX13 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Synthetic peptide contain a sequence corresponding to a region within amino acids 342 and 403 of Human PEX13

Anwendungsinformationen

Applikationshinweise: Suggested dilutions:
Western blotting: 1.500-1.3000

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 PEX13

Target: PEX13 (Peroxisomal Biogenesis Factor 13 (PEX13))

Andere Bezeichnung: Peroxin 13 (PEX13 Produkte)

Synonyme: CG4663 antikoerper, DmelPex13 antikoerper, Dmel\\CG4663 antikoerper, pex13 antikoerper, zgc:66124 antikoerper, PAS20 antikoerper, DDBDRAFT_0191662 antikoerper, DDBDRAFT_0238077 antikoerper, DDB_0191662 antikoerper, DDB_0238077 antikoerper, NALD antikoerper, PBD11A antikoerper, PBD11B antikoerper, ZWS antikoerper, 2610008O20Rik antikoerper, Peroxin 13 antikoerper, peroxisomal biogenesis factor 13 antikoerper, peroxin PEX13 antikoerper, peroxin 13 (predicted) antikoerper, peroxin antikoerper, SH3 domain-containing protein antikoerper, putative peroxin 13 antikoerper, peroxisome biogenesis factor 13 antikoerper, Pex13 antikoerper, pex13 antikoerper, PEX13 antikoerper

Hintergrund: This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm.Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome.[provided by RefSeq]

Molekulargewicht: 44 kDa

Gen-ID: 5194

NCBI Accession: NM_002618, NP_002609

Pathways: Feeding Behaviour, Monocarboxylic Acid Catabolic Process