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NSJ Bioreagents
SKU:RQ5795
Arylsulfatase L Antibody / ARSL
Arylsulfatase L Antibody / ARSL
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$449.00 USD
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Arylsulfatase L is an enzyme that, in humans, is encoded by the ARSL gene. It 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.
Specifications
| Family | Primary antibody |
|---|---|
| Formulation | 0.5mg/ml if reconstituted with 0.2ml sterile DI water |
| Format | Antigen affinity purified |
| Host Animal | Rabbit |
| Clonality | Polyclonal (rabbit origin) |
| Isotype | Rabbit IgG |
| Species Reactivity | Human, Monkey |
| Application | WB |
| Application Details | Western blot: 0.5-1ug/ml |
| Application Note | Optimal dilution of the Arylsulfatase L antibody should be determined by the researcher. |
| Immunogen | Amino acids FYQVMERVQQAVWEHQR from the human protein were used as the immunogen for the Arylsulfatase L antibody. |
| Buffer | Lyophilized from 1X PBS with 2% Trehalose and 0.025% sodium azide |
| Purity | Affinity purified |
| Storage | After reconstitution, the Arylsulfatase L antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing. |
| Limitation | This Arylsulfatase L antibody is available for research use only. |
| Uniprot # | P51690 |
| Status | Available |
| PDF Link | https://www.nsjbio.com/tds-pdf/arylsulfatase-l-antibody-arsl-rq5795 |
| Title | Arylsulfatase L Antibody / ARSL |
| Description | Arylsulfatase L is an enzyme that, in humans, is encoded by the ARSL gene. It 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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