CNBD2 Antikörper (AA 21-120) (FITC)

Produktnummer ABIN1710201

Dieses Anti-CNBD2-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von CNBD2 in WB, IF (cc) und IF (p). Geeignet für Human.

Kurzübersicht für CNBD2 Antikörper (AA 21-120) (FITC) (ABIN1710201)

Target: CNBD2 (Cyclic Nucleotide Binding Domain Containing 2 (CNBD2))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CNBD2 Antikörper ist konjugiert mit FITC

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

Produktdetails anti-CNBD2 Antikörper (FITC)

Bindungsspezifität: AA 21-120

Kreuzreaktivität: Human

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf152

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 CNBD2

Target: CNBD2 (Cyclic Nucleotide Binding Domain Containing 2 (CNBD2))

Andere Bezeichnung: C20orf152

Hintergrund:

Synonyms: C20orf152, Chromosome 20 open reading frame 152, CT152_HUMAN, dJ954P9.1, RP5-954P9.1, Uncharacterized protein C20orf152, Uncharacterized protein C20orf152 homolog.

Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf152 gene product has been provisionally designated C20orf152 pending further characterization.

Gen-ID: 140894