Arylsulfatase E Antikörper (C-Term)

Produktnummer ABIN2854321

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch Arylsulfatase E in WB. Es zeigt Reaktivität gegenüber Proben von Human.

Kurzübersicht für Arylsulfatase E Antikörper (C-Term) (ABIN2854321)

Target: Arylsulfatase E (ARSE)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Arylsulfatase E Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-Arylsulfatase E Antikörper

Bindungsspezifität: C-Term

Kreuzreaktivität: Human

Produktmerkmale: Rabbit polyclonal antibody to ASE (arylsulfatase E (chondrodysplasia punctata 1))
ASE antibody [C2C3], C-term

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the C-terminus region of human ARSE. The exact sequence is proprietary.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Konservierungsmittel: Thimerosal (Merthiolate)

Vorsichtsmaßnahmen: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Details zu Arylsulfatase E

Target: Arylsulfatase E (ARSE)

Andere Bezeichnung: arylsulfatase E

Hintergrund: Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene.

Cellular Localization: Golgi apparatus , Golgi stack

Molekulargewicht: 66 kDa

Gen-ID: 415

UniProt: P51690