EPM2AIP1 Antikörper (N-Term)

Produktnummer ABIN2856551

Produktdetails anti-EPM2AIP1 Antikörper

Target: EPM2AIP1 (EPM2A (Laforin) Interacting Protein 1 (EPM2AIP1))

Bindungsspezifität: N-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser EPM2AIP1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Kreuzreaktivität: Human

Produktmerkmale: Rabbit polyclonal antibody to EPM2AIP1 (EPM2A (laforin) interacting protein 1)
EPM2AIP1 antibody [N1], N-term

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Carrier-protein conjugated synthetic peptide encompassing a sequence within the N-terminus region of human EPM2AIP1. The exact sequence is proprietary.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Kommentare:

Positive Control: 293T , A431 , H1299

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Konservierungsmittel: Thimerosal (Merthiolate)

Vorsichtsmaßnahmen: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Details zu EPM2AIP1

Target: EPM2AIP1 (EPM2A (Laforin) Interacting Protein 1 (EPM2AIP1))

Andere Bezeichnung: EPM2A interacting protein 1 (EPM2AIP1 Produkte)

Synonyme: EPM2AIP1 antikoerper, DKFZp459D2251 antikoerper, A930003G21Rik antikoerper, mKIAA0766 antikoerper, EPM2A interacting protein 1 antikoerper, EPM2A (laforin) interacting protein 1 antikoerper, EPM2AIP1 antikoerper, Epm2aip1 antikoerper

Hintergrund: The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless.

Cellular Localization: Endoplasmic reticulum

Molekulargewicht: 70 kDa

Gen-ID: 9852

UniProt: Q7L775