CCZ1 Antikörper (AbBy Fluor® 750)

Produktnummer ABIN4999383

Produktdetails anti-CCZ1 Antikörper (AbBy Fluor® 750)

Target: CCZ1 (CCZ1 Vacuolar Protein Trafficking and Biogenesis Associated Homolog (S. Cerevisiae) (CCZ1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CCZ1 Antikörper ist konjugiert mit AbBy Fluor® 750

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

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCZ1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 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 CCZ1

Target: CCZ1 (CCZ1 Vacuolar Protein Trafficking and Biogenesis Associated Homolog (S. Cerevisiae) (CCZ1))

Andere Bezeichnung: CCZ1 (CCZ1 Produkte)

Synonyme: C7orf28A antikoerper, CCZ1A antikoerper, H_DJ1163J12.2 antikoerper, AU022870 antikoerper, C25H7orf28A antikoerper, zgc:55344 antikoerper, CCZ1 homolog, vacuolar protein trafficking and biogenesis associated antikoerper, CCZ1 vacuolar protein trafficking and biogenesis associated antikoerper, CCZ1 antikoerper, Ccz1 antikoerper, ccz1 antikoerper

Hintergrund:

Synonyms: C7orf28A, CCZ1 vacuolar protein trafficking and biogenesis associated homolog S. cerevisiae, CCZ1A, CGI-43, H_DJ1163J12.2, Vacuolar fusion protein CCZ1 homolog, CCZ1_HUMAN.

Background: Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5 % of the human genome. 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 C7orf28 gene product has been provisionally designated C7orf28 pending further characterization.