PDCD10 Antikörper

Produktnummer ABIN6989859

Produktdetails anti-PDCD10 Antikörper

Target: PDCD10 (Programmed Cell Death 10 (PDCD10))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PDCD10 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF)

Kreuzreaktivität: Human, Maus

Aufreinigung: Purified by Protein A.

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-212 of human PDCD10 (NP_009148.2).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IF()

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C for 12 months.

Haltbarkeit: 12 months

Details zu PDCD10

Target: PDCD10 (Programmed Cell Death 10 (PDCD10))

Andere Bezeichnung: PDCD10 (PDCD10 Produkte)

Synonyme: CCM3 antikoerper, TFAR15 antikoerper, 2410003B13Rik antikoerper, Ccm3 antikoerper, Tfa15 antikoerper, Tfar15 antikoerper, zgc:85629 antikoerper, ccm3a antikoerper, pdcd10 antikoerper, zgc:65826 antikoerper, programmed cell death 10 antikoerper, programmed cell death 10 S homeolog antikoerper, programmed cell death 10b antikoerper, programmed cell death 10a antikoerper, PDCD10 antikoerper, Pdcd10 antikoerper, pdcd10.S antikoerper, pdcd10b antikoerper, pdcd10a antikoerper

Hintergrund:

Synonyms: PDCD10,CCM3,TFAR15

Background: This gene encodes an evolutionarily conserved protein associated with cell apoptosis. The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway. It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent. Mutations in this gene are one cause of cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages. Multiple alternatively spliced variants, encoding the same protein, have been identified.

Gen-ID: 11235

UniProt: Q9BUL8