PLEKHH2 Rekombinanter Antikörper

PLEKHH2 Rekombinant Antikörper für WB, ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human

Anwendung

WB, ELISA

Konjugation

Unkonjugiert

CloneNo.

250291H8

Kat-Nr. : 86166-3-RR

Synonyme

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

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  WB analysis of human kidney using 86166-3-RR

  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.

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  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.

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Geprüfte Anwendungen

• Erfolgreiche Detektion in WB: humanes Nierengewebe

Empfohlene Verdünnung

• Western Blot (WB): WB : 1:1000-1:4000

It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Sample-dependent, check data in validation data gallery

Produktinformation

86166-3-RR bindet in WB, 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 Molekulargewicht: 168 kDa
• GenBank-Zugangsnummer: BC063310
• Gene symbol: PLEKHH2
• Gene ID (NCBI): 130271
• Konjugation: Unkonjugiert
• Form: Liquid
• Reinigungsmethode: Protein-A-Reinigung
• Lagerungspuffer: PBS with 0.02% sodium azide and 50% glycerol
• Lagerungsbedingungen: Bei -20°C lagern. Nach dem Versand ein Jahr lang stabil Aliquotieren ist bei -20^oC Lagerung nicht notwendig. 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.