Shiga Toxin 1 & 2 (Stx-1, Stx-2) Antikörper

Produktnummer ABIN648008

Der Maus Anti--Antikörper wurde für validiert. Er ist geeignet, in Proben von E. coli zu detektieren.

Kurzübersicht für Shiga Toxin 1 & 2 (Stx-1, Stx-2) Antikörper (ABIN648008)

Target: Shiga Toxin 1 & 2 (Stx-1, Stx-2)

Reaktivität: E. coli

Wirt: Maus

Konjugat: Unkonjugiert

Applikation: Bitte anfragen

Produktdetails

Spezifität: Reacts with Escherichia coli (E. coli) Shigatoxin (STX) 1 and 2

Produktmerkmale: Mouse Anti-E. coli STX 1 & 2

Aufreinigung: Purified

Isotyp: IgG

Anwendungsinformationen

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Rekonstitution: Reconstitute with 1ml deionized water.

Konzentration: 1 mg/ml (prior to lyophilization)

Buffer: Lyophilized from 5mM Phosphate buffer, pH 7.2 - 7.4

Lagerung: 4 °C

Antigendetails

Target: Shiga Toxin 1 & 2 (Stx-1, Stx-2)

Hintergrund: Monoclonal Antibody to Escherichia coli (E. coli) Shigatoxin (STX) 1 and 2, pooled IgGThe baculovirus protein p35 inhibits virally induced apoptosis of invertebrate and mammalian cells and may function to impair the clearing of virally infected cells by the host's immune system. This is accomplished at least in part by its ability to block both TNF- and FAS-mediated apoptosis through the inhibition of the ICE family of serine proteases. Two mammalian homologs of baculovirus p35, referred to as inhibitor of apoptosis protein (IAP) 1 and 2, share an amino terminal baculovirus IAP repeat (BIR) motif and a carboxy terminal RING finger. Although the c-IAPs do not directly associate with the TNF receptor (TNF-R), they efficiently block TNF-mediated apoptosis through their interaction with the downstream TNF-R effectors, TRAF1 and TRAF2. Additional IAP family members include ILP (for IAP-like protein) and survivin. ILP inhibits activated caspase-3, leading to the resistance of FAS-mediated apoptosis. Survivin (also designated TIAP) is expressed during the G2/M phase of the cell cycle and associates with microtublules of the mitotic spindle. Increased caspase-3 activity is detected when a disruption of survivin-microtubule interactions occurs.