Ciprofloxacin(CIP) antibody/antigen (BSA/OVA/KLH conjugated hapten)

anti-Ciprofloxacin(CIP) antibody and Carrier-coupled antigen/immunogen (hapten-carrier conjugates)

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Product information

Catalog No.DescriptionUS $ Price (per mg)
GMP-SMT-54-11. BSA-Ciprofloxacin(CIP)
2. Anti-Ciprofloxacin(CIP) mouse monoclonal antibody
$2709.00
GMP-SMT-54-21. OVA-Ciprofloxacin(CIP)
2. Anti-Ciprofloxacin(CIP) mouse monoclonal antibody
$2709.00
GMP-SMT-54-31. BSA-Ciprofloxacin(CIP)
2. Anti-Ciprofloxacin(CIP) human monoclonal antibody
$2709.00
GMP-SMT-54-41. OVA-Ciprofloxacin(CIP)
2. Anti-Ciprofloxacin(CIP) human monoclonal antibody
$2709.00
GMP-SMT-54-Ag-1BSA-Ciprofloxacin(CIP)$756.00
GMP-SMT-54-Ag-2OVA-Ciprofloxacin(CIP)$756.00
GMP-SMT-54-Ab-1Anti-Ciprofloxacin(CIP) mouse monoclonal antibody$1953.00
GMP-SMT-54-Ab-2Anti-Ciprofloxacin(CIP) human monoclonal antibody$1953.00

Size: 1mg | 10mg | 100mg



Product Description


BSA-Ciprofloxacin(CIP)

Cat No.GMP-SMT-54-Ag-1
Bioactivity validationCompetitive immunoassay validation (Competitive ELISA) with hapten-carrier conjugates and anti-Hapten antibody;
Products descriptionCompetitive immunoassay-validated hapten-carrier conjugates BSA-Ciprofloxacin(CIP) with anti-Hapten antibody. The hapten hapten-carrier conjugates BSA-Ciprofloxacin(CIP) had been validated with our anti-Hapten antibody Anti-Ciprofloxacin(CIP) mouse monoclonal antibody via competitive ELISA test.
ApplicationELISA tests and other immunoassays;
Lateral flow immunoassay (LFIA);
LTIA
Immunonephelometry
Time-resolved Fluorescence Immunoassay (TRFIA)
FormulationLyophilized from sterile PBS, PH 7.4
StorageStore at -20℃ to -80℃ under sterile conditions. Avoid repeated freeze-thaw cycles.


OVA-Ciprofloxacin(CIP)

Cat No.GMP-SMT-54-Ag-2
Bioactivity validationCompetitive immunoassay validation (Competitive ELISA) with hapten-carrier conjugates and anti-Hapten antibody;
Products descriptionCompetitive immunoassay-validated hapten-carrier conjugates OVA-Ciprofloxacin(CIP) with anti-Hapten antibody. The hapten hapten-carrier conjugates OVA-Ciprofloxacin(CIP) had been validated with our anti-Hapten antibody Anti-Ciprofloxacin(CIP) mouse monoclonal antibody via competitive ELISA test.
ApplicationELISA tests and other immunoassays;
Lateral flow immunoassay (LFIA);
LTIA
Immunonephelometry
Time-resolved Fluorescence Immunoassay (TRFIA)
FormulationLyophilized from sterile PBS, PH 7.4
StorageStore at -20℃ to -80℃ under sterile conditions. Avoid repeated freeze-thaw cycles.


Anti-Ciprofloxacin(CIP) mouse monoclonal antibody

Cat No.GMP-SMT-54-Ab-1
Host of AntibodyMouse IgG
Bioactivity validationCompetitive immunoassay validation (Competitive ELISA) with hapten-carrier conjugates and anti-Hapten antibody;
Lateral flow immunoassay (LFIA);
ELISA IC50 (ppb)0.3-0.5
Products descriptionThe anti-Hapten antibody against hapten Ciprofloxacin(CIP) had been validated with our hapten hapten-carrier conjugates BSA-Ciprofloxacin(CIP) via competitive ELISA test.
ApplicationELISA tests and other immunoassays;
Lateral flow immunoassay (LFIA);
LTIA
Immunonephelometry
Time-resolved Fluorescence Immunoassay (TRFIA)
FormulationLyophilized from sterile PBS, PH 7.4
StorageStore at -20℃ to -80℃ under sterile conditions. Avoid repeated freeze-thaw cycles.


Anti-Ciprofloxacin(CIP) human monoclonal antibody

Cat No.GMP-SMT-54-Ab-2
Host of AntibodyHuman IgG1
Bioactivity validationCompetitive immunoassay validation (Competitive ELISA) with hapten-carrier conjugates and anti-Hapten antibody;
Lateral flow immunoassay (LFIA);
ELISA IC50 (ppb)0.3-0.5
Products descriptionThe anti-Hapten antibody against hapten Ciprofloxacin(CIP) had been validated with our hapten hapten-carrier conjugates BSA-Ciprofloxacin(CIP) via competitive ELISA test.
ApplicationELISA tests and other immunoassays;
Lateral flow immunoassay (LFIA);
LTIA
Immunonephelometry
Time-resolved Fluorescence Immunoassay (TRFIA)
FormulationLyophilized from sterile PBS, PH 7.4
StorageStore at -20℃ to -80℃ under sterile conditions. Avoid repeated freeze-thaw cycles.


Reference




    Validation Data


    Click to get more Data / Case study about the product.



    Biomarker Information


    1. Introduction:

    Ciprofloxacin (CIP), a member of the fluoroquinolone class of antibiotics, has garnered significant attention in recent years due to its dual role in pharmaceutical applications and environmental impact. This versatile compound, originally developed for clinical use, has found its way into the environment through various pathways, posing potential ecological and public health concerns. In this comprehensive exploration, we delve into the multifaceted dimensions of CIP, shedding light on its origin, environmental significance, methods of measurement, and the implications it holds for both ecosystems and human health.

    2. Understanding Ciprofloxacin (CIP):

    2.1 Pharmaceutical Application:

    CIP is widely prescribed to treat a spectrum of bacterial infections in humans, demonstrating its effectiveness against a range of pathogens. Its mechanism of action involves inhibiting the enzymes necessary for DNA replication, making it a potent antimicrobial agent.

    2.2 Environmental Introduction:

    The widespread use of CIP in healthcare facilities and subsequent excretion by patients leads to its introduction into wastewater systems. Additionally, improper disposal of unused medications and agricultural runoff contribute to its presence in natural water bodies. This influx of CIP into the environment raises concerns due to its potential impact on aquatic life and the development of antibiotic-resistant strains of bacteria.

    3. Environmental Significance of Ciprofloxacin (CIP):

    3.1 Ecological Impact:

    CIP, classified as an emerging environmental contaminant, can disrupt aquatic ecosystems. Its presence in water bodies affects aquatic organisms, including fish and amphibians, leading to adverse physiological effects and potential population imbalances.

    3.2 Antibiotic Resistance Concerns:

    CIP residues in the environment contribute to the development of antibiotic-resistant bacteria. These resistant strains pose a significant threat to public health, as they can compromise the effectiveness of antibiotics in treating infections, leading to prolonged illnesses and increased mortality rates.

    4. Methods of CIP Measurement:

    4.1 Environmental Monitoring Techniques:

    Accurate measurement of CIP levels in environmental samples is crucial for understanding its distribution and impact. Advanced analytical techniques, such as high-performance liquid chromatography (HPLC) and mass spectrometry, enable scientists to quantify trace amounts of CIP in various environmental matrices, providing valuable data for research and regulatory purposes.

    4.2 Wastewater Treatment Evaluation:

    Monitoring CIP levels in wastewater treatment plants assesses the efficacy of treatment processes. Proper treatment is essential to ensure the removal of pharmaceutical residues, preventing their release into natural water bodies. Regular evaluation helps optimize treatment methods, minimizing environmental contamination.

    5. Implications for Human Health:

    5.1 Drinking Water Contamination:

    CIP's presence in natural water sources raises concerns about its potential entry into drinking water supplies. While conventional water treatment methods can remove many contaminants, the persistence of CIP necessitates continuous monitoring to safeguard public health.

    5.2 Health Impact Assessment:

    Exposure to low levels of CIP through contaminated water or food sources raises questions about its long-term effects on human health. Research is ongoing to comprehensively assess the potential risks, emphasizing the need for stringent regulations and monitoring protocols.

    6. Conclusion:

    In conclusion, Ciprofloxacin (CIP), a potent antibiotic vital for human health, has inadvertently become a significant environmental concern. Its introduction into natural ecosystems and the subsequent development of antibiotic-resistant bacteria underscore the complex interplay between human activities, pharmaceutical usage, and environmental health. As our understanding of CIP's impact deepens, continued research, rigorous monitoring, and regulatory measures are imperative to mitigate its adverse effects on both ecosystems and human populations. Only through collective efforts can we navigate the intricate challenges posed by CIP and safeguard the delicate balance of our environment and public health.



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