CMSS1 Antikörper (AbBy Fluor® 594)

Produktnummer ABIN2810821

Der Kaninchen Polyklonal Anti-CMSS1-Antikörper wurde für WB validiert. Er ist geeignet, CMSS1 in Proben von Human, Maus und Ratte zu detektieren.

Kurzübersicht für CMSS1 Antikörper (AbBy Fluor® 594) (ABIN2810821)

Target: CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CMSS1 Antikörper ist konjugiert mit AbBy Fluor® 594

Applikation: Western Blotting (WB)

Produktdetails anti-CMSS1 Antikörper (AbBy Fluor® 594)

Kreuzreaktivität: Human

Homologie: Mouse,Rat,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C3orf26

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: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: 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 CMSS1

Target: CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))

Andere Bezeichnung: C3orf26

Hintergrund:

Synonyms: C3orf26, CC026_HUMAN, MGC4308, Uncharacterized protein C3orf26.

Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The C3orf26 gene product has been provisionally designated C3orf26 pending further characterization.