CCDC169 Antikörper (AbBy Fluor® 750)

Produktnummer ABIN4997910

Produktdetails anti-CCDC169 Antikörper (AbBy Fluor® 750)

Target: CCDC169 (Coiled-Coil Domain Containing 169 (CCDC169))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CCDC169 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 C13orf38

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 CCDC169

Target: CCDC169 (Coiled-Coil Domain Containing 169 (CCDC169))

Andere Bezeichnung: C13orf38 (CCDC169 Produkte)

Synonyme: C13orf38 antikoerper, A730037C10Rik antikoerper, c13orf38 antikoerper, coiled-coil domain containing 169 antikoerper, coiled-coil domain containing 169 S homeolog antikoerper, CCDC169 antikoerper, Ccdc169 antikoerper, ccdc169.S antikoerper

Hintergrund:

Synonyms: FLJ57222, Chromosome 13 open reading frame 38, CM038_HUMAN, FLJ13506, FLJ29024, Hypothetical protein LOC728591, RP11-251J8.1, UPF0594 protein C13orf38.

Background: Comprising nearly 4 % of human DNA, chromosome 13 contains around 114 million base pairs and 400 genes. Key tumor suppressor genes on chromosome 13 include the breast cancer susceptibility gene, BRCA2, and the RB1 (retinoblastoma) gene. RB1 encodes a crucial tumor suppressor protein which, when defective, leads to malignant growth in the retina and has been implicated in a variety of other cancers. The gene SLITRK1, which is associated with Tourette syndrome, is on chromosome 13. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is quite deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections. The LOC728591 gene product has been provisionally designated LOC728591 pending further characterization.