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The antibody against ARSE was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 520-589 of human ARSE (NP_000038.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
The antibody against ARSE was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 520-589 of human ARSE (NP_000038.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
| Cat.No | ADA-00585A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | ARSE |
| Target Synonyms | ASE; ARSE; CDPX; CDPX1; CDPXR | Form | Liquid |
| Species Reactivity | Mouse, Rat | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.01% thimerosal, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | Mouse liver, Rat liver | Application | ELISA, WB |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 520-589 of human ARSE (NP_000038.2). | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | PSETHILTPASEPVFYQVMERVQQAVWEHQRTLSPVPLQLDRLGNIWRPWLQPCCGPFPLCWCLREDDPQ | Uniprot ID | P51690 |
Uniprot Id
P51690
Target Species
Human
Target Name
ARSL
Target Full Name
Arylsulfatase L
Target Function
Exhibits arylsulfatase activity towards the artifical substrate 4-methylumbelliferyl sulfate. May be essential for the correct composition of cartilage and bone matrix during development. Has no activity toward steroid sulfates.
Target Involvement
Chondrodysplasia punctata 1, X-linked recessive (CDPX1)
Target Subcellular Location
Golgi apparatus, Golgi stack.
Target Protein Families
Sulfatase family
Target Tissue Specificity
Expressed in the pancreas, liver and kidney.
Target Synonyms
ARSL; ARSE; Arylsulfatase L; EC 3.1.6.-; Arylsulfatase E; ASE
Target 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. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome.
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