C7orf42 Antikörper (AA 231-314) (Cy5.5)

Produktnummer ABIN1706061

Dieses Anti-C7orf42-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von C7orf42 in WB, IF (cc) und IF (p). Geeignet für Human.

Kurzübersicht für C7orf42 Antikörper (AA 231-314) (Cy5.5) (ABIN1706061)

Target: C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C7orf42 Antikörper ist konjugiert mit Cy5.5

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

Produktdetails anti-C7orf42 Antikörper (Cy5.5)

Bindungsspezifität: AA 231-314

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf42

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 C7orf42

Target: C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))

Andere Bezeichnung: C7orf42

Hintergrund:

Synonyms: C7orf42, TM248_HUMAN, Chromosome 7 open reading frame 42, FLJ10099, FLJ13090, Hypothetical protein LOC55069, UPF0458 protein C7orf42.

Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf42 gene product has been provisionally designated C7orf42 pending further characterization.

Gen-ID: 55069