C2orf24 Antikörper

Produktnummer ABIN1387180

Produktdetails anti-C2orf24 Antikörper

Target: C2orf24 (Chromosome 2 Open Reading Frame 24 (C2orf24))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C2orf24 Antikörper ist unkonjugiert

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

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C2orf24

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Informationen zur Lagerung: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Haltbarkeit: 12 months

Details zu C2orf24

Target: C2orf24 (Chromosome 2 Open Reading Frame 24 (C2orf24))

Andere Bezeichnung: C2orf24 (C2orf24 Produkte)

Synonyme: c2orf24 antikoerper, wu:fa05h07 antikoerper, zgc:55857 antikoerper, MGC75999 antikoerper, C12H2orf24 antikoerper, MGC115028 antikoerper, DKFZp459J1014 antikoerper, C2orf24 antikoerper, CGI-57 antikoerper, C2H2orf24 antikoerper, C7H2orf24 antikoerper, 1810031K17Rik antikoerper, AU043960 antikoerper, RGD735175 antikoerper, cyclin Pas1/PHO80 domain containing 1 antikoerper, cyclin Pas1/PHO80 domain containing 1 L homeolog antikoerper, cnppd1 antikoerper, CNPPD1 antikoerper, cnppd1.L antikoerper, Cnppd1 antikoerper

Hintergrund:

Synonyms: CDABP0125, CGI 57, chromosome 2 open reading frame 24, CNPD1_HUMAN, CNPPD1, Cyclin Pas1/PHO80 domain-containing protein 1, Protein CNPPD1.

Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf24 gene product has been provisionally designated C2orf24 pending further characterization.

Gen-ID: 27013