Arylsulfatase E Polyclonal Antibody
Sizes: 50μL, 100μL
Catalogue Numbers: RA22103-50, RA22103-100
Citations, Manuals and MSDS Available upon request.
Background: arylsulfatase E (chondrodysplasia punctata 1) (ARSE) Homo sapiens 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. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome. [provided by RefSeq, Sep 2013],
Condition: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Storage Instructions: -20°C/1 year
Recommended dilutions: Western Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
Alternative Names: ARSE; Arylsulfatase E; ASE
Applications: WB; ELISA
Species Cross-Reactivity: Human; Rat; Mouse
GeneID (Human): 415
Protein MW (KDa): 65
SWISS: P51690
Source: Rabbit
Research Use Only