NRARP Antikörper (AA 41-114) (Cy5.5)

Produktnummer ABIN1411961

Der Kaninchen Polyklonal Anti-NRARP-Antikörper wurde für WB, IF (cc) und IF (p) validiert. Er ist geeignet, NRARP in Proben von Human zu detektieren.

Kurzübersicht für NRARP Antikörper (AA 41-114) (Cy5.5) (ABIN1411961)

Target: NRARP (NOTCH-Regulated Ankyrin Repeat Protein (NRARP))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NRARP Antikörper ist konjugiert mit Cy5.5

Applikation: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Produktdetails anti-NRARP Antikörper (Cy5.5)

Bindungsspezifität: AA 41-114

Homologie: Human,Mouse,Rat,Cow,Sheep,Pig,Chicken

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human NRARP

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu NRARP

Target: NRARP (NOTCH-Regulated Ankyrin Repeat Protein (NRARP))

Andere Bezeichnung: NRARP

Hintergrund:

Synonyms: MGC61598, Notch regulated ankyrin repeat containing protein, NOTCH regulated ankyrin repeat protein, Notch-regulated ankyrin repeat-containing protein, nrarp, NRARP_HUMAN.

Background: Nrarp (NOTCH-regulated ankyrin repeat protein) is a 114 amino acid protein that contains two ANK repeats and is thought to play a role in the formation of somites. The gene encoding Nrarp maps to human chromosome 9, which contains 145 million base pairs and comprises 4 % of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia and Familial dysautonomia are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukemias.