C7ORF57 Antikörper (AA 161-260) (HRP)

Produktnummer ABIN1711862

Produktdetails anti-C7ORF57 Antikörper (HRP)

Target: C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))

Bindungsspezifität: AA 161-260

Reaktivität: Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C7ORF57 Antikörper ist konjugiert mit HRP

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

Kreuzreaktivität: Ratte

Homologie: Human,Mouse,Cow,Sheep,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf57

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 C7ORF57

Target: C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))

Andere Bezeichnung: C7orf57 (C7ORF57 Produkte)

Synonyme: C7orf57 antikoerper, chromosome 4 open reading frame, human C7orf57 antikoerper, chromosome 7 open reading frame 57 antikoerper, C4H7orf57 antikoerper, C7orf57 antikoerper

Hintergrund:

Synonyms: C7orf57, CG057_HUMAN, Chromosome 7 open reading frame 57, Uncharacterized protein C7orf57.

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 C7orf57 gene product has been provisionally designated C7orf57 pending further characterization.

Gen-ID: 136288

UniProt: Q8NEG2