ZC2HC1C Antikörper (Cy5.5)

Produktnummer ABIN1421527

Produktdetails anti-ZC2HC1C Antikörper (Cy5.5)

Target: ZC2HC1C (Zinc Finger, C2HC-Type Containing 1C (ZC2HC1C))

Reaktivität: Human, Ratte, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ZC2HC1C Antikörper ist konjugiert mit Cy5.5

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 C14ORF140/FAM164C

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 ZC2HC1C

Target: ZC2HC1C (Zinc Finger, C2HC-Type Containing 1C (ZC2HC1C))

Andere Bezeichnung: C14ORF140 (ZC2HC1C Produkte)

Synonyme: C14orf140 antikoerper, FAM164C antikoerper, 2810002I04Rik antikoerper, AV046379 antikoerper, Fam164c antikoerper, RGD1307122 antikoerper, zinc finger C2HC-type containing 1C antikoerper, zinc finger, C2HC-type containing 1C antikoerper, ZC2HC1C antikoerper, Zc2hc1c antikoerper

Hintergrund:

Synonyms: chromosome 14 open reading frame 140, FAM164C, family with sequence similarity 164 member C, FLJ23093, UPF0418 protein FAM164C, ZC21C_HUMAN.

Background: Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5 % of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein BCL3 in the (14,19) translocations found in a variety of B cell malignancies. The C14orf140 gene product has been provisionally designated C14orf140 pending further characterization.