Arylsulfatase E anticorps (AA 120-200)

N° du produit ABIN7222378

Cet anticorps anti-Arylsulfatase E Polyclonal Lapin (ABIN7222378) détecte spécifiquement Arylsulfatase E dans ELISA et WB. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour Arylsulfatase E anticorps (AA 120-200) (ABIN7222378)

Antigène: Arylsulfatase E (ARSE)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Arylsulfatase E est non-conjugé

Application: ELISA, Western Blotting (WB)

Détail du produit anti-Arylsulfatase E anticorps

Épitope: AA 120-200

Fonction: Rabbit Anti-Arylsulfatase E Polyclonal Antibody

Specificité: Arylsulfatase E Polyclonal Antibody detects endogenous levels of Arylsulfatase E protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from the Internal region of human Arylsulfatase E at AA range: 120-200

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,ELISA 1:10000,Not yet tested in other applications.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur Arylsulfatase E

Antigène: Arylsulfatase E (ARSE)

Autre désignation: Arylsulfatase E

Sujet: ARSE, Arylsulfatase E, ASEArylsulfatase 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. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome.

Poids moléculaire: 65kD

ID gène: 415

UniProt: P51690