NDE1 Antikörper (AA 270-350)

Produktnummer ABIN7229926

Dieser Anti-NDE1 Antikörper ist ein Kaninchen Polyklonal Antikörper zur Detektion von NDE1 in WB und ELISA. Geeignet für Human, Maus und Ratte.

Kurzübersicht für NDE1 Antikörper (AA 270-350) (ABIN7229926)

Target: NDE1

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NDE1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-NDE1 Antikörper

Bindungsspezifität: AA 270-350

Verwendungszweck: NDE1 Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of NDE1 protein

Aufreinigung: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogen: Synthesized peptide derived from part region of human NDE1 protein at AA range: 270-350

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Kommentare:

Primary Antibody

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Details zu NDE1

Target: NDE1

Andere Bezeichnung: NDE1

Hintergrund: Rabbit Anti-NDE1 Polyclonal Antibody,Nuclear distribution protein nudE homolog 1, NudE,NDE1 (NudE Neurodevelopment Protein 1) encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe cognitive disability. Alternative splicing results in multiple transcript variants. Among its related pathways are Regulation of PLK1 Activity at G2/M Transition and Cell Cycle, Mitotic.,NDE1

Molekulargewicht: observerd band 38kDa

Gen-ID: 54820

UniProt: Q9NXR1