CASC5 Antikörper

Produktnummer ABIN6567781

Produktdetails anti-CASC5 Antikörper

Target: CASC5 (Cancer Susceptibility Candidate 5 (CASC5))

Reaktivität: Human, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CASC5 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC)

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human CASC5 (NP_733468.3).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000 IHC 1:50-1:100

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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. Avoid freeze / thaw cycles.

Details zu CASC5

Target: CASC5 (Cancer Susceptibility Candidate 5 (CASC5))

Andere Bezeichnung: CASC5 (CASC5 Produkte)

Synonyme: AF15Q14 antikoerper, CT29 antikoerper, D40 antikoerper, KNL1 antikoerper, PPP1R55 antikoerper, Spc7 antikoerper, hKNL-1 antikoerper, hSpc105 antikoerper, 2310043D08Rik antikoerper, 5730505K17Rik antikoerper, Rad51 antikoerper, kinetochore scaffold 1 antikoerper, Kinetochore null protein 1 antikoerper, KNL1 antikoerper, Knl1 antikoerper, knl-1 antikoerper

Hintergrund: The protein encoded by this gene is a component of the multiprotein assembly that is required for creation of kinetochore-microtubule attachments and chromosome segregation. The encoded protein functions as a scaffold for proteins that influence the spindle assembly checkpoint during the eukaryotic cell cycle and it interacts with at least five different kinetochore proteins and two checkpoint kinases. In adults, this gene is predominantly expressed in normal testes, various cancer cell lines and primary tumors from other tissues and is ubiquitously expressed in fetal tissues. This gene was originally identified as a fusion partner with the mixed-lineage leukemia (MLL) gene in t(11,15)(q23,q14). Mutations in this gene cause autosomal recessive primary microcephaly-4 (MCPH4). Alternative splicing results in multiple transcript variants encoding different isoforms. Additional splice variants have been described but their biological validity has not been confirmed.

Molekulargewicht:

Observed_MW: 300kDa

Calculated_MW: 195kDa/205kDa/262kDa/265kDa

Gen-ID: 57082

UniProt: Q8NG31

Pathways: Maintenance of Protein Location, Autophagie