ARSB Polyclonal Antibody (E-AB-16264)

For research use only.
Verified Samples |
Verified Samples in IHC: Human breast cancer, Human brain |
Dilution | IHC 1:50-1:200 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human |
Applications | IHC |
Clonality | Polyclonal |
Immunogen | Synthetic peptide of human ARSB |
Abbre | ARSB |
Synonyms | ARSB, ASB, Arsb, Arylsulfatase B, ArylsulfataseB, G4S, MPS6, N acetylgalactosamine 4 sulfatase, N-acetylgalactosamine-4-sulfatase |
Swissprot | |
Cellular Localization | Lysosome. |
Concentration | 0.7 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Affinity purification |
Research Areas | Cancer, Metabolism, Signal transduction |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
background | Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targetted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. |
Other Clones
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Other Formats
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Unconjugated
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