

Product description
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 o
Source
Rabbit
Applications
WB,ELISA
Reactivity
Human
Dilution
WB: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
Storage
-20°C/1 year
Specificity
Arylsulfatase E Polyclonal Antibody detects endogenous levels of Arylsulfatase E protein.
Source/Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Immunogen
Synthesized peptide derived from Arylsulfatase E . at AA range: 120-200
Uniprot No
P51690
Alternative names
ARSE; Arylsulfatase E; ASE
Form
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Clonality
Polyclonal
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 o
Other
Gene_name: ARSE ; Protein_name: Arylsulfatase E; Expression: Kidney,Kidney proximal tubule,Liver,Pancreas,
Mol.Wt (Da)
65 kD
Concentration
1 mg/ml
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