C7orf43 Antikörper (AA 301-400) (HRP)

Produktnummer ABIN1710949

Produktdetails anti-C7orf43 Antikörper (HRP)

Target: C7orf43 (Chromosome 7 Open Reading Frame 43 (C7orf43))

Bindungsspezifität: AA 301-400

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C7orf43 Antikörper ist konjugiert mit HRP

Applikation: Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7ORF43

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC-P 1:200-400
IHC-F 1:100-500

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.

Handhabung: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

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 C7orf43

Target: C7orf43 (Chromosome 7 Open Reading Frame 43 (C7orf43))

Andere Bezeichnung: C7ORF43 (C7orf43 Produkte)

Synonyme: chromosome 3 open reading frame, human C7orf43 antikoerper, chromosome 7 open reading frame 43 antikoerper, C3H7orf43 antikoerper, c7orf43 antikoerper, C7orf43 antikoerper

Hintergrund:

Synonyms: C7orf43, CG043_HUMAN, Chromosome 7 open reading frame 43, DKFZp761G0712, FLJ10925, Hypothetical protein LOC55262, Uncharacterized protein C7orf43.

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 C7orf43 gene product has been provisionally designated C7orf43 pending further characterization.

Gen-ID: 55262