Arylsulfatase A Antikörper

Produktnummer ABIN2854547

Produktdetails anti-Arylsulfatase A Antikörper

Target: Arylsulfatase A (ARSA)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Arylsulfatase A Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Kreuzreaktivität: Human

Produktmerkmale: Rabbit Polyclonal antibody to Arylsulfatase A
Arylsulfatase A antibody [N2C2], Internal

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human Arylsulfatase A. 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.

Kommentare:

Positive Control: H1299 , HeLa

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.44 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 A

Target: Arylsulfatase A (ARSA)

Andere Bezeichnung: arylsulfatase A (ARSA Produkte)

Synonyme: ARSA antikoerper, zgc:101575 antikoerper, arsa antikoerper, AS-A antikoerper, ASA antikoerper, AW212749 antikoerper, As-2 antikoerper, As2 antikoerper, TISP73 antikoerper, MLD antikoerper, mld antikoerper, arylsulfatase A antikoerper, arylsulfatase antikoerper, arylsulfatase A, gene 1 S homeolog antikoerper, ARSA antikoerper, arsa antikoerper, arsA antikoerper, RB6599 antikoerper, Arsa antikoerper, arsa.1.S antikoerper

Hintergrund: The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Multiple alternatively spliced transcript variants, one of which encodes a distinct protein, have been described for this gene.

Cellular Localization: Lysosome

Molekulargewicht: 54 kDa

Gen-ID: 410

UniProt: P15289