Human Arylsulfatase B  ELISA Kit

Human Arylsulfatase B ELISA Kit

IHUARSBKT

Innovative Research

  • $534.00


This Human Arylsulfatase B ELISA Kit from Innovative Research is intended for quantitative detection of human ARSB in cell culture supernates, serum and plasma (heparin, EDTA, citrate). Strip well format. Reagents for up to 96 tests.

This human ARSB ELISA Kit is based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from mouse specific for ARSB has been precoated onto 96-well plates. Standards(Expression system for standard: NSO, Immunogen sequence: S37-M533) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for ARSB is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex is added and unbound conjugates are washed away with PBS or TBS buffer. HRP substrate TMB are used to visualize HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the human ARSB amount of sample captured in plate.

  • Detection Target: Arylsulfatase B
  • Uniprot ID: P15848)
  • Reactivity: Human
  • Cross-Reactivity: There is no detectable cross-reactivity with other relevant proteins.
  • Range: 15.6pg/ml-1000pg/ml
  • Sensitivity: <10pg/ml
  • Storage Conditions: Store at 4?C for 6 months, at -20?C for 12 months. Avoid multiple freeze-thaw cycles. (Shipped with wet ice)

Additional Information: The capture antibody is a monoclonal antibody from mouse, the detection antibody is a biotinylated polyclonal antibody from goat. Expression system for standard: Arylsulfatase B is an enzyme associated with mucopolysaccharidosis VI. It is mapped to 5q14.1. 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 targeted 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.; Immunogen sequence: 369

Product References
Product Disclaimer

This material is sold for in-vitro use only for manufacturing and research. This material is not suitable for human or animal use. While we make every effort to ensure the safety of our products, we recommend handling any biological materials with standard precautions as if capable of spreading infectious disease. The statements herin are offered for informational purposes only to be used solely for your consideration, investigation, and verification.

Please be aware the image pictured is for illustrative purposes only, and your product packaging and appearance may vary.

Questions? Contact us about this product!

Get in touch with our team! Please include any relevant information (product name, etc)


We Also Recommend

×