BEAN1 Antikörper (AA 10-70) (Alexa Fluor 594)

Produktnummer ABIN2810253

Produktdetails anti-BEAN1 Antikörper (Alexa Fluor 594)

Target: BEAN1 (Brain Expressed, Associated with NEDD4, 1 (BEAN1))

Bindungsspezifität: AA 10-70

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser BEAN1 Antikörper ist konjugiert mit Alexa Fluor 594

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

Homologie: Human,Mouse,Rat,Dog,Cow,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human BEAN1

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 BEAN1

Target: BEAN1 (Brain Expressed, Associated with NEDD4, 1 (BEAN1))

Andere Bezeichnung: BEAN1/SCA31 (BEAN1 Produkte)

Synonyme: BEAN antikoerper, SCA31 antikoerper, Bean antikoerper, brain expressed associated with NEDD4 1 antikoerper, brain expressed, associated with Nedd4, 1 antikoerper, BEAN1 antikoerper, Bean1 antikoerper

Hintergrund:

Synonyms: BEAN, Bean1, BEAN1_HUMAN, Brain-expressed protein associating with Nedd4 homolog, Protein BEAN1, SCA31.

Background: The protein encoded by this gene is one of several proteins that interact with NEDD4, a member of a family of ubiquitin-protein ligases. These proteins have PY motifs in common that bind to the WW domains of NEDD4. NEDD4 is developmentally regulated, and is highly expressed in embryonic tissues. Mutations in this gene (i.e., intronic insertions of >100 copies of pentanucleotide repeats including a (TGGAA)n sequence) are associated with spinocerebellar ataxia type 31. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010].