SERPING1 Antikörper

Produktnummer ABIN7259610

Produktdetails anti-SERPING1 Antikörper

Target: SERPING1 (Serpin Peptidase Inhibitor, Clade G (C1 Inhibitor), Member 1 (SERPING1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SERPING1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human C1 Inactivator (NP_001027466.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:1000-1:2000 IF 1:50-1:200

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 SERPING1

Target: SERPING1 (Serpin Peptidase Inhibitor, Clade G (C1 Inhibitor), Member 1 (SERPING1))

Andere Bezeichnung: C1 Inactivator (SERPING1 Produkte)

Synonyme: fb64f02 antikoerper, im:7159527 antikoerper, si:dkeyp-110g5.2 antikoerper, wu:fb60c09 antikoerper, wu:fb62a08 antikoerper, wu:fb64f02 antikoerper, LOC100136072 antikoerper, C1-INH antikoerper, C1INH antikoerper, C1nh antikoerper, C1IN antikoerper, C1NH antikoerper, HAE1 antikoerper, HAE2 antikoerper, serpin peptidase inhibitor, clade G (C1 inhibitor), member 1 antikoerper, C1 inhibitor antikoerper, serpin family G member 1 antikoerper, serine (or cysteine) peptidase inhibitor, clade G, member 1 antikoerper, serping1 antikoerper, LOC100136072 antikoerper, SERPING1 antikoerper, Serping1 antikoerper

Hintergrund: This gene encodes a highly glycosylated plasma protein involved in the regulation of the complement cascade. Its protein inhibits activated C1r and C1s of the first complement component and thus regulates complement activation. Deficiency of this protein is associated with hereditary angioneurotic oedema (HANE). Alternative splicing results in multiple transcript variants encoding the same isoform.

Molekulargewicht:

Observed_MW: 60 kDa.110 kDa

Calculated_MW: 49 kDa/55 kDa

Gen-ID: 710

UniProt: P05155

Pathways: Komplementsystem