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PEX16 Monoklonaler Antikörper

PEX16 Monoklonal Antikörper für WB, Indirect ELISA

Wirt / Isotyp

Maus / IgG1

Getestete Reaktivität

human, Maus, Ratte

Anwendung

WB, Indirect ELISA

Konjugation

Unkonjugiert

CloneNo.

2D7G4

Kat-Nr. : 68261-1-PBS

Synonyme

Peroxin 16, PEX16

Filter:
  • Western Blot (WB) analysis of various lysates using PEX16 Monoclonal antibody (68261-1-Ig)

    WB analysis using 68261-1-Ig (same clone as 68261-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 68261-1-Ig (PEX16 antibody) at dilution of 1:10000 and incubated at room temperature for 1.5 hours. The membrane was stripped and reblotted with HRP-conjugated Beta Actin Monoclonal antibody (HRP-66009) as loading control. This data was developed using the same antibody clone with 68261-1-PBS in a different storage buffer formulation.

Geprüfte Anwendungen

Produktinformation

68261-1-PBS bindet in WB, Indirect ELISA PEX16 und zeigt Reaktivität mit human, Maus, Ratten

Getestete Reaktivität human, Maus, Ratte
Wirt / Isotyp Maus / IgG1
Klonalität Monoklonal
Typ Antikörper
Immunogen PEX16 fusion protein Ag6574
Vollständiger Name peroxisomal biogenesis factor 16
Berechnetes Molekulargewicht 39 kDa
Beobachtetes Molekulargewicht 38 kDa
GenBank-ZugangsnummerBC000467
Gene symbol PEX16
Gene ID (NCBI) 9409
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Protein-G-Reinigung
Lagerungspuffer PBS only
LagerungsbedingungenStore at -80°C. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. Peroxin 16, also known as PEX16 or Peroxisomal biogenesis factor 16, is a 336 amino acid integral membrane protein that has a critical role in the biogenesis of peroxisomes. PEX16 together with PEX3 and PEX19 are specifically involved in peroxisomal membrane protein (PMP) import. Defects in the gene encoding Peroxin 16 are the cause of multiple peroxisome-related disorders, including Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), classical rhizomelic chondrodysplasia punctata (RCDP) and peroxisome biogenesis disorder complementation group 9 (PBD-CG9).