SLMAP Antikörper (AA 25-607)

Produktnummer ABIN7872886

Der Kaninchen Polyklonal anti-SLMAP Antikörper (ABIN7872886) detektiert spezifisch SLMAP in WB, ELISA und FACS. Dieser Antikörper reagiert spezifisch mit Proben aus Human und Maus.

Kurzübersicht für SLMAP Antikörper (AA 25-607) (ABIN7872886)

Target: SLMAP (Sarcolemma Associated Protein (SLMAP))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SLMAP Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Produktdetails anti-SLMAP Antikörper

Bindungsspezifität: AA 25-607

Verwendungszweck: SLMAP Antibody / Sarcolemmal membrane-associated protein

Aufreinigung: Antigen affinity purified

Immunogen: E. coli-derived recombinant human protein (amino acids D25-E607) was used as the immunogen for the SLMAP antibody.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the SLMAP 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 SLMAP 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 SLMAP

Target: SLMAP (Sarcolemma Associated Protein (SLMAP))

Andere Bezeichnung: SLMAP

Hintergrund: Sarcolemmal membrane-associated protein is a protein that in humans is encoded by the SLMAP gene. This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants.

UniProt: Q14BN4