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ARMC4 Rekombinanter Antikörper

ARMC4 Rekombinant Antikörper für WB, Indirect ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus

Anwendung

WB, Indirect ELISA

Konjugation

Unkonjugiert

CloneNo.

241122G4

Kat-Nr. : 84004-3-PBS

Synonyme

RP11 691I13.1, Outer dynein arm-docking complex subunit 2, ODAD2, Armadillo repeat-containing protein 4, armadillo repeat containing 4

Filter:
  • Western Blot (WB) analysis of mouse testis tissue using ARMC4 Recombinant antibody (84004-3-RR)

    WB analysis of mouse testis using 84004-3-RR (same clone as 84004-3-PBS)

    mouse testis tissue were subjected to SDS PAGE followed by western blot with 84004-3-RR (ARMC4 antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 84004-3-PBS in a different storage buffer formulation.

  • Affinity and Kinetic Characterization of 84004-3-RR

    Affinity and Kinetic Characterization of 84004-3-RR

    Biolayer interferometry (BLl) kinetic assays of 84004-3-RR against Human ARMC4 were performed. The affinity constant is 1.29 nM.

Geprüfte Anwendungen

Produktinformation

84004-3-PBS bindet in WB, Indirect ELISA ARMC4 und zeigt Reaktivität mit human, Maus

Getestete Reaktivität human, Maus
Wirt / Isotyp Kaninchen / IgG
Klonalität Rekombinant
Typ Antikörper
Immunogen ARMC4 fusion protein Ag22340
Vollständiger Name armadillo repeat containing 4
Berechnetes Molekulargewicht 1044 aa, 116 kDa
Beobachtetes Molekulargewicht116 kDa
GenBank-ZugangsnummerBC140846
Gene symbol ODAD2
Gene ID (NCBI) 55130
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Protein A purfication
Lagerungspuffer PBS only
LagerungsbedingungenStore at -80°C. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

ODAD2 contains ten Armadillo repeat motifs (ARMs) and one HEAT repeat, and is thought to be involved in ciliary and flagellar movement. This protein has been shown to localize to the ciliary axonemes and at the ciliary base of respiratory cells. Studies indicate that mutations in this gene cause partial outer dynein arm (ODA) defects in respiratory cilia. The cilia of cells with mutations in this gene displayed either reduced ciliary beat frequency and amplitude, or, complete immotility. Some individuals with primary ciliary dyskensia (PCD) have been shown to have mutations in this gene. PCD is characterized by chronic airway disease and left/right body asymmetry defects.