Arylsulfatase E antibody

Catalog No. ABIN2458596

Product Details anti-Arylsulfatase E Antibody

Target: Arylsulfatase E (ARSE)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Arylsulfatase E antibody is un-conjugated

Application: ELISA, Western Blotting (WB)

Purification: Antibody is purified by peptide affinity chromatography method.

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

Application Details

Application Notes: 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

Handling

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.

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

Storage: 4 °C/-20 °C

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

Target Details for Arylsulfatase E

Target: Arylsulfatase E (ARSE)

Alternative Name: ARSE (ARSE Products)

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

Background: 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.

Molecular Weight: 62 kDa

Gene ID: 415

NCBI Accession: NP_000038

UniProt: P51690