IQCA1 Antikörper (FITC)

Produktnummer ABIN1400378

Produktdetails anti-IQCA1 Antikörper (FITC)

Target: IQCA1 (IQ Motif Containing with AAA Domain 1 (IQCA1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser IQCA1 Antikörper ist konjugiert mit FITC

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 IQCA1

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 IQCA1

Target: IQCA1 (IQ Motif Containing with AAA Domain 1 (IQCA1))

Andere Bezeichnung: IQCA1 (IQCA1 Produkte)

Synonyme: 4930465P12Rik antikoerper, 4930585L22Rik antikoerper, BB288505 antikoerper, Iqca1 antikoerper, IQCA antikoerper, RGD1305311 antikoerper, IQ motif containing with AAA domain antikoerper, IQ motif containing with AAA domain 1 antikoerper, Iqca antikoerper, IQCA1 antikoerper, Iqca1 antikoerper

Hintergrund:

Synonyms: IQ and AAA domain-containing protein 1, IQ mot containing with AAA domain 1, IQCA, Iqca1, IQCA1_HUMAN, RGD1305311, FLJ22527, 4930465P12Rik, FLJ33588.

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.