MANBA anticorps

N° du produit ABIN2855559

Cet anticorps anti-MANBA est un anticorps Lapin Polyclonal détectant MANBA dans WB. Adapté pour Humain.

Aperçu rapide pour MANBA anticorps (ABIN2855559)

Antigène: MANBA (Mannosidase, beta A, Lysosomal (MANBA))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MANBA est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-MANBA anticorps

Réactivité croisée: Humain

Attributs du produit: Rabbit polyclonal antibody to MANBA (mannosidase, beta A, lysosomal)
MANBA antibody [N3C2], Internal

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human MANBA. 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: HepG2

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 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 MANBA

Antigène: MANBA (Mannosidase, beta A, Lysosomal (MANBA))

Autre désignation: mannosidase beta

Sujet: This gene encodes a member of the glycosyl hydrolase 2 family. The encoded protein localizes to the lysosome where it is the final exoglycosidase in the pathway for N-linked glycoprotein oligosaccharide catabolism. Mutations in this gene are associated with beta-mannosidosis, a lysosomal storage disease that has a wide spectrum of neurological involvement.

Cellular Localization: Lysosome

Poids moléculaire: 101 kDa

ID gène: 4126

UniProt: O00462