C2ORF44 Antikörper (AbBy Fluor® 680)

Produktnummer ABIN4998383

Produktdetails anti-C2ORF44 Antikörper (AbBy Fluor® 680)

Target: C2ORF44 (Chromosome 2 Open Reading Frame 44 (C2ORF44))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C2ORF44 Antikörper ist konjugiert mit AbBy Fluor® 680

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 C2orf44

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 C2ORF44

Target: C2ORF44 (Chromosome 2 Open Reading Frame 44 (C2ORF44))

Andere Bezeichnung: C2orf44 (C2ORF44 Produkte)

Synonyme: A430092C04 antikoerper, WD repeat and coiled coil containing antikoerper, WD repeat and coiled coil containing L homeolog antikoerper, WDCP antikoerper, wdcp.L antikoerper, Wdcp antikoerper

Hintergrund:

Synonyms: C2orf44, CB044_HUMAN, Chromosome 2 open reading frame 44, FLJ21945, PP384, WD repeat-containing protein C2orf44.

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 C2orf44 gene product has been provisionally designated C2orf44 pending further characterization.

Gen-ID: 80304