Arylsulfatase E antibody (C-Term)

Catalog No. ABIN2854321

Product Details anti-Arylsulfatase E Antibody

Target: Arylsulfatase E (ARSE)

Binding Specificity: C-Term

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Arylsulfatase E antibody is un-conjugated

Application: Western Blotting (WB)

Cross-Reactivity: Human

Characteristics: Rabbit polyclonal antibody to ASE (arylsulfatase E (chondrodysplasia punctata 1))
ASE antibody [C2C3], C-term

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the C-terminus region of human ARSE. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for Arylsulfatase E

Target: Arylsulfatase E (ARSE)

Alternative Name: arylsulfatase E (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.

Cellular Localization: Golgi apparatus , Golgi stack

Molecular Weight: 66 kDa

Gene ID: 415

UniProt: P51690