Arylsulfatase B Antikörper

Produktnummer ABIN2854408

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch Arylsulfatase B in WB. Er zeigt eine Reaktivität gegenüber Human.

Kurzübersicht für Arylsulfatase B Antikörper (ABIN2854408)

Target: Arylsulfatase B (ARSB)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Arylsulfatase B Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-Arylsulfatase B Antikörper

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Rabbit polyclonal antibody to ARSB (arylsulfatase B)
ARSB antibody [N3C3]

Aufreinigung: Affinity purified by Protein A.

Immunogen: Recombinant protein encompassing a sequence within the center region of human ARSB. 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: ARSB transfected 293T cell , HeLa , HepG2 , mouse placenta , rat testis

Validation: Overexpression

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 6.11 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 B

Target: Arylsulfatase B (ARSB)

Andere Bezeichnung: arylsulfatase B

Hintergrund: Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targetted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.

Cellular Localization: Lysosome

Molekulargewicht: 60 kDa

Gen-ID: 411

UniProt: P15848

Pathways: Glycosaminoglycan Metabolic Process