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BD 222601 - Salmonella O Antisera F G RP Factor High-Quality Reagent for Salmonella Serological Identification, EA

BD  # 222601 - Salmonella O Antisera F G RP Factor  High-Quality Reagent for Salmonella Serological Identification, EA
Part Number BD 222601
SKU Number CIA1127943
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List Price $234.45
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Product Description

BD 222601 - Salmonella O Antisera F G RP Factor High-Quality Reagent for Salmonella Serological Identification, EA

The BD 222601 Salmonella O Antisera F G RP Factor is a high-performance serological reagent specifically designed for the accurate identification and differentiation of Salmonella species based on their somatic (O) antigens. Manufactured under the trusted BD Difco and BBL quality standards, this antisera reagent is an essential component in the comprehensive serotyping of Salmonella isolates according to the Kauffmann-White classification scheme. The reagent ensures reliable agglutination results, supporting precise and consistent bacterial typing for diagnostic, public health, and food safety laboratories.

Key Benefits

The BD 222601 Salmonella O Antisera F G RP Factor offers exceptional specificity, accuracy, and reproducibility in bacterial serological testing. Its high-titer formulation enables clear and rapid agglutination, allowing laboratories to identify Salmonella O antigen groups with confidence. Each lot is standardized for potency and performance to eliminate variability between tests. The reagents high purity and stability ensure long shelf life, while its ready-to-use format saves preparation time and reduces laboratory error during routine testing procedures.

Compatibility and Applications

This antisera reagent is compatible with standard slide or tube agglutination methods and is used in conjunction with other BD Salmonella antisera reagents to achieve complete serogroup and serotype identification. It is designed for use with cultured bacterial isolates grown on non-selective agar media such as nutrient agar or tryptic soy agar. The BD 222601 reagent is ideal for use in clinical microbiology laboratories, food safety testing facilities, veterinary laboratories, and public health institutions monitoring Salmonella outbreaks and epidemiological patterns.

Usage Guidelines

Before testing, ensure that the bacterial culture is fresh and derived from a pure isolate. Perform agglutination testing using standard procedures: place one drop of the BD 222601 antisera on a clean glass slide, emulsify a portion of the bacterial colony into the drop, and observe for visible agglutination within one minute. A positive reaction indicates the presence of the specific Salmonella O antigen group corresponding to factors F, G, or related subgroups. Always include appropriate positive and negative controls for validation. Store the reagent at 28C and avoid freezing to maintain potency.

Certifications, Safety Standards, and Regulatory Approvals

The BD 222601 Salmonella O Antisera F G RP Factor is manufactured in ISO 13485 and ISO 9001 certified facilities, ensuring compliance with stringent international quality standards. It is CE-marked and FDA-registered for in vitro diagnostic use. Each batch undergoes rigorous quality assurance testing for sterility, specificity, and reactivity, meeting the performance standards outlined by the World Health Organization (WHO) and the Centers for Disease Control and Prevention (CDC) for Salmonella serotyping reagents.

Comparison with Competitor Products

Compared to generic antisera reagents, BDs Salmonella O Antisera series provides superior clarity, consistency, and rapid agglutination results. Competitor reagents may exhibit weaker reactions or non-specific agglutination, leading to uncertain interpretations. BDs formulation ensures optimal antibody concentration, reducing false positives or negatives and allowing clear differentiation between closely related Salmonella serogroups. Laboratories worldwide prefer BD antisera for their reliability and alignment with international reference standards.

Typical User Profile and Application Scenarios

The BD 222601 Salmonella O Antisera F G RP Factor is primarily used by microbiologists, laboratory technologists, and epidemiologists engaged in bacterial identification and outbreak surveillance. Common applications include foodborne pathogen testing, clinical infection diagnosis, veterinary screening, and research in bacterial taxonomy. It is also essential in public health reference laboratories conducting Salmonella typing to trace sources of infection and ensure food and water safety.

Best Practices for Use and Maintenance

For consistent and accurate results, always handle the reagent under aseptic conditions and use clean, grease-free glass slides. Allow refrigerated reagents to equilibrate to room temperature before use. Avoid contamination by using sterile droppers or pipettes. Replace the cap immediately after dispensing to prevent evaporation or contamination. Periodically verify reagent performance with known control strains to maintain confidence in test accuracy. Discard any reagent showing precipitation or discoloration.

Regulatory and Safety Information

The BD 222601 Salmonella O Antisera F G RP Factor is intended for in vitro diagnostic use only by trained laboratory professionals. It is classified as non-hazardous but should be handled in accordance with standard biosafety procedures. Avoid ingestion or contact with skin and eyes, and wear appropriate personal protective equipment (PPE) such as gloves and lab coats during testing. Dispose of all used materials and bacterial cultures as biohazard waste according to institutional and regional regulations.

How to Order

To order the BD 222601 Salmonella O Antisera F G RP Factor, add the product to your cart and complete your purchase through CIA Medicals secure online checkout system. For bulk orders, institutional supply agreements, or detailed technical specifications, contact CIA Medical customer service at (312) 275-5850 or submit your inquiry through the contact form on this page. Our support team can assist with product availability, pricing, and guidance for integration into your laboratorys serotyping workflows.