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PLEKHH2 Rekombinanter Antikörper

PLEKHH2 Rekombinant Antikörper für WB, Indirect ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human

Anwendung

WB, Indirect ELISA

Konjugation

Unkonjugiert

CloneNo.

250291H8

Kat-Nr. : 86166-3-PBS

Synonyme

KIAA2028, Pleckstrin homology domain-containing family H member 2, PLEKHH1L

Filter:
  • Western Blot (WB) analysis of human kidney tissue using PLEKHH2 Recombinant antibody (86166-3-RR)

    WB analysis of human kidney using 86166-3-RR (same clone as 86166-3-PBS)

    human kidney tissue were subjected to SDS PAGE followed by western blot with 86166-3-RR (PLEKHH2 antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 86166-3-PBS in a different storage buffer formulation.

  • Affinity and Kinetic Characterization of 86166-3-RR

    Affinity and Kinetic Characterization of 86166-3-RR

    Biolayer interferometry (BLl) kinetic assays of 86166-3-RR against Human PLEKHH2 were performed. The affinity constant is 6.03 nM.

Geprüfte Anwendungen

Produktinformation

86166-3-PBS bindet in WB, Indirect ELISA PLEKHH2 und zeigt Reaktivität mit human

Getestete Reaktivität human
Wirt / Isotyp Kaninchen / IgG
Klonalität Rekombinant
Typ Antikörper
Immunogen PLEKHH2 fusion protein Ag5409
Vollständiger Name pleckstrin homology domain containing, family H (with MyTH4 domain) member 2
Berechnetes Molekulargewicht 168 kDa
Beobachtetes Molekulargewicht168 kDa
GenBank-ZugangsnummerBC063310
Gene symbol PLEKHH2
Gene ID (NCBI) 130271
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Protein-A-Reinigung
Lagerungspuffer PBS only
LagerungsbedingungenStore at -80°C. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

PLEKHH2 is a 1491-residue intracellular protein highly enriched in renal glomerular podocytes. PLEKHH2 is one of two previously uncharacterized PLEKHH proteins encoded in the mammalian genomes. A PLEKHH ortholog has also been described in Drosophila, Caenorhabditis elegans, and zebrafish. In C. elegans, the loss of the protein was found to cause variable axon guidance defects.