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Mouse Anti-Pseudomonas aeruginosa Monoclonal Antibody

Cat. No.VD11Y36

Product TypeVeterinary Antibodies

Size

Product Overview

BioVenic mouse monoclonal antibody is specific for Pseudomonas aeruginosa. It was produced in hybridoma and subsequently assessed for purity using SDS-PAGE. It can be applied to ELISA and lateral flow immunoassay to diagnose Pseudomonas aeruginosa infection in equine. The clone N07Y71 can be used as capture antibody in the ELISA assay, and the clone N07Y72 can be used as detection antibody in the ELISA assay.

Specifications

Application ELISA; LF
Clonality Monoclonal Antibody
Classification Primary Antibody
Clone N07Y71; N07Y72
Host Mouse
Target Species Bacteria
Species Reactivity Equine
Specificity Pseudomonas aeruginosa
Isotype IgG
Immunogen Inactive whole-cell Pseudomonas aeruginosa.
Purity ≥ 95% (SDS-PAGE)
Conjugation Unconjugated
Buffer 1X Phosphate buffered saline, pH 7.4
Physical State Lyophilized

Target Information

Pseudomonas aeruginosa is a Gram-negative bacterium known for its adaptability and versatility. Pseudomonas aeruginosa is a leading cause of healthcare-associated infections. It can cause infections in wounds, the respiratory tract, the urinary tract, and other sites, especially in individuals with weakened immune systems.

Target Pseudomonas aeruginosa
Target Synonym P. aeruginosa
Taxonomy ID 287

Shipping and Storage

This product is shipped with dry ice. Store at -20°C to -80°C on receipt (up to 12 months). Avoid repeated freezing and thawing as this may denature the antibody.

Documents

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

User Note

  1. The clone N07Y71 can be used as capture antibody in the ELISA assay, and N07Y72 can be used as detection antibody in the ELISA assay.

References

  1. Poole, Keith. "Pseudomonas aeruginosa: resistance to the max." Frontiers in microbiology 2 (2011): 65.
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