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Anti-ARSA Antibody (9A5)
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Catalog No. TMAY-00845
Alias TISP73, AW212749, AS-A, ASA, As-2, As2, arylsulfatase A
Anti-ARSA Antibody (9A5) is a Rabbit antibody targeting ARSA. Anti-ARSA Antibody (9A5) can be used in ELISA.
Anti-ARSA Antibody (9A5)
Anti-ARSA Antibody (9A5)
😃Good
Catalog No. TMAY-00845Alias TISP73, AW212749, AS-A, ASA, As-2, As2, arylsulfatase A
Anti-ARSA Antibody (9A5) is a Rabbit antibody targeting ARSA. Anti-ARSA Antibody (9A5) can be used in ELISA.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 100 μL | $270 | 7-10 days |
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Product Introduction
Bioactivity
Related Conjugates and Formulations
Antigen Details
Chemical Properties
| Description | Anti-ARSA Antibody (9A5) is a Rabbit antibody targeting ARSA. Anti-ARSA Antibody (9A5) can be used in ELISA. |
| Alias | TISP73, AW212749, AS-A, ASA, As-2, As2, arylsulfatase A |
| Ig Type | Monoclonal Rabbit IgG |
| Clone | 9A5 |
| Reactivity | Human |
| Application | ELISA |
| Recommended Dose | ELISA: 1:1000-1:2000 |
| Antibody Type | Monoclonal |
| Host Species | Rabbit |
| Construction | This antibody was obtained from a rabbit immunized with purified, recombinant Human Arylsulfatase A / ARSA (rh Arylsulfatase A / ARSA; TMPY-00669; P15289-1; Met 1-Ala 507). |
| Purification | Protein A |
| Appearance | Liquid |
| Formulation | 0.2 μm filtered solution in PBS |
| Research Background | Arylsulfatase A (ARSA) is synthesized as a 52KDa lysosomal enzyme. It is a member of the sulfatase family that is required for the lysosomal degradation of cerebroside-3-sulfate, a sphingolipid sulfate ester and a major constituent of the myelin sheet. Arylsulfatase A is activated by a required co- or posttranslational modification with the oxidation of cysteine to formylglycine. Metachromatic leukodystrophy (MLD) is a lysosomal storage disease in the central and peripheral nervous systems with severe and progressive neurological symptoms caused by the deficiency of Arylsulfatase A. Deficiency of this enzyme is also found in apparently healthy individuals, a condition for which the term pseudodeficiency is introduced. ARSA forms dimers after receiving three N-linked oligosaccharides in the endoplasmic reticulum, and then the dimers are transported to the Golgi where they receive mannose 6-phosphate recognition markers. And thus, ARSA is transported and delivered to dense lysosomes in a mannose 6-phosphate receptor-dependent manner. It has been shown that within the lysosomes, the ARSA dimers can oligomerize to an octamer in a pH-dependent manner. The ARSA deficiency leads to metachromatic leucodystrophy (MLD), a lysosomal storage disorder associated with severe and progressive demyelination in he central and peripheral nervous system. Additionally, the serum level of arylsulfatase A might be helpful in diagnosis of lung and central nervous system cancer. |
| Conjucates | Unconjugated |
| Immunogen | Recombinant Human Arylsulfatase A / ARSA protein (TMPY-00669) |
| Antigen Species | Human |
Stability & Storage
| Stability & Storage | Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. Preservative-Free. |
| Transport | Shipping with blue ice. |
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