CCDC36 Antikörper (AA 172-472)

Produktnummer ABIN7871265

Der Kaninchen Polyklonal anti-CCDC36 Antikörper wird verwendet zum Nachweis von CCDC36 in Proben von Human. Er wurde validiert für WB, ELISA und IHC (p).

Kurzübersicht für CCDC36 Antikörper (AA 172-472) (ABIN7871265)

Target: CCDC36 (Coiled-Coil Domain Containing 36 (CCDC36))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CCDC36 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Produktdetails anti-CCDC36 Antikörper

Bindungsspezifität: AA 172-472

Verwendungszweck: CCDC36 Antibody

Aufreinigung: Antigen affinity purified

Immunogen: Amino acids E172-N472 from the human protein were used as the immunogen for the CCDC36 antibody.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the CCDC36 antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: After reconstitution, the CCDC36 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Details zu CCDC36

Target: CCDC36 (Coiled-Coil Domain Containing 36 (CCDC36))

Andere Bezeichnung: CCDC36

Hintergrund: CCDC36, also known as CT74 (cancer/testis antigen 74), is a 584 amino acid protein that contains coiled-coil domains and is expressed as three alternatively spliced isoforms. The gene encoding CCDC36 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the 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.

UniProt: Q8IYA8