FAM209B Antikörper (PE)

Produktnummer ABIN1712668

Dieser Kaninchen Polyklonal Antikörper erkennt spezifisch FAM209B in WB. Er zeigt eine Reaktivität gegenüber Human.

Kurzübersicht für FAM209B Antikörper (PE) (ABIN1712668)

Target: FAM209B (Family with Sequence Similarity 209, Member B (FAM209B))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FAM209B Antikörper ist konjugiert mit PE

Applikation: Western Blotting (WB)

Produktdetails anti-FAM209B Antikörper (PE)

Homologie: Human

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf107

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: FCM(1:20-100)

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: 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: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu FAM209B

Target: FAM209B (Family with Sequence Similarity 209, Member B (FAM209B))

Andere Bezeichnung: C20orf107

Hintergrund:

Synonyms: C20orf107, Chromosome 20 open reading frame 107, CT107_HUMAN, dJ1153D9.4, Hypothetical protein LOC388799, MGC104273, Uncharacterized protein C20orf107.

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 C20orf107 gene product has been provisionally designated C20orf107 pending further characterization.

Gen-ID: 388799