Arylsulfatase A anticorps

N° du produit ABIN2854547

Détail du produit anti-Arylsulfatase A anticorps

Antigène: Arylsulfatase A (ARSA)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Arylsulfatase A est non-conjugé

Application: Western Blotting (WB)

Réactivité croisée: Humain

Attributs du produit: Rabbit Polyclonal antibody to Arylsulfatase A
Arylsulfatase A antibody [N2C2], Internal

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human Arylsulfatase A. The exact sequence is proprietary.

Isotype: IgG

Information d'application

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

Commentaires:

Positive Control: H1299 , HeLa

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.44 mg/mL

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

Agent conservateur: Thimerosal (Merthiolate)

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

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Détails sur Arylsulfatase A

Antigène: Arylsulfatase A (ARSA)

Autre désignation: arylsulfatase A (ARSA Produits)

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

Sujet: 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

Poids moléculaire: 54 kDa

ID gène: 410

UniProt: P15289