Arylsulfatase E anticorps (Middle Region)

N° du produit ABIN1449829

Cet anticorps Lapin Polyclonal détecte spécifiquement Arylsulfatase E dans WB. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour Arylsulfatase E anticorps (Middle Region) (ABIN1449829)

Antigène: Arylsulfatase E (ARSE)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Arylsulfatase E est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Arylsulfatase E anticorps

Épitope: Middle Region

Séquence: KVVHHDPPLL FDLSRDPSET HILTPASEPV FYQVMERVQQ AVWEHQRTLS

Réactivité croisée (Details): Species reactivity (tested):Human

Purification: Purified using peptide immunoaffinity column

Immunogène: Synthetic peptide directed towards the middle region of human ARSE

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Reconstitution: Add 50 μL of distilled water to a final concentration of 1 mg/mL.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store lyophilized at 2-8 °C for one month or at -20 °C long term. After reconstitution store the antibody undiluted at 2-8 °C for up to one month or in aliquots at -20 °C long term.

Détails sur Arylsulfatase E

Antigène: Arylsulfatase E (ARSE)

Autre désignation: Arylsulfatase E

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.Synonyms: ARSE, ASE

ID gène: 415

NCBI Accession: NP_000038