Arylsulfatase E anticorps

N° du produit ABIN2458596

Détail du produit anti-Arylsulfatase E anticorps

Antigène: Arylsulfatase E (ARSE)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Arylsulfatase E est non-conjugé

Application: ELISA, Western Blotting (WB)

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ARSE.

Information d'application

Indications d'application: ARSE antibody can be used for detection of ARSE by ELISA at 1:62500. ARSE antibody can be used for detection of ARSE by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store ARSE antibody at -20 °C.

Détails sur Arylsulfatase E

Antigène: Arylsulfatase E (ARSE)

Autre désignation: ARSE (ARSE Produits)

Synonymes: anticorps ASE, anticorps CDPX, anticorps CDPX1, anticorps CDPXR, anticorps ARSE, anticorps MGC155058, anticorps arylsulfatase E (chondrodysplasia punctata 1), anticorps arylsulfatase E, anticorps ARSE, anticorps Arse

Sujet: 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.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.

Poids moléculaire: 62 kDa

ID gène: 415

NCBI Accession: NP_000038

UniProt: P51690