Arylsulfatase E Antikörper

Produktnummer ABIN2458596

Produktdetails anti-Arylsulfatase E Antikörper

Target: Arylsulfatase E (ARSE)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Arylsulfatase E Antikörper ist unkonjugiert

Applikation: ELISA, Western Blotting (WB)

Aufreinigung: Antibody is purified by peptide affinity chromatography method.

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

Anwendungsinformationen

Applikationshinweise: 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.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

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

Konzentration: 1 mg/mL

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

Handhabung: As with any antibody avoid repeat freeze-thaw cycles.

Lagerung: 4 °C/-20 °C

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

Details zu Arylsulfatase E

Target: Arylsulfatase E (ARSE)

Andere Bezeichnung: ARSE (ARSE Produkte)

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

Hintergrund: 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.

Molekulargewicht: 62 kDa

Gen-ID: 415

NCBI Accession: NP_000038

UniProt: P51690