clia / elisa, rapid test
Anti-Hepatitis B virus (HBeAg) hepatitis b clia / elisa rapid test
Item Number : HBeAg
Price varies based on specs and customizations
- Diseases
- hepatitis b
- Application
- clia / elisa , rapid test
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Product Overview Table
| Feature | Description |
|---|---|
| Product Name | Anti-Hepatitis B virus (HBeAg) |
| Application | LF / ELISA |
| Form/Appearance | Purified from mouse ascites by protein A chromatography |
| Concentration | ≥ 1 mg/ml |
| Isotype | IgG1 |
| Clonality | Monoclonal |
| Purity | ≥ 90% |
| Buffer | 0.01M Phosphate Buffered Saline, pH 7.2, containing 0.1% sodium azide |
| Cross Reactivity | Not determined |
| Specificity | Hepatitis B “e” antigen |
Storage and Transportation Conditions Table
| Condition | Description |
|---|---|
| Storage | 2-8°C or -20°C. Avoid freeze-thaws. Maximum one freeze-thaw during storage. |
| Shipping | Cold packs |
| Shelf Life | Four years from date of manufacture |
Finished Product Performance Indicator Table
| Indicator | Acceptance Criteria |
|---|---|
| Package Appearance | Product outer packaging box, aluminum foil packaging bag should be complete and without damage. |
| Test Strip Appearance | Clean and flat, no burrs, no damage, no pollution; material attached firmly. |
| Test Strip Width | Width should not exceed ±0.20mm of the nominal value, with a nominal value of 4.00mm. |
| Migration Speed | Liquid migration speed should not be less than 10mm/min. |
| Minimum Detection Limit (HBeAg) | Results should meet the requirements when tested with the HBeAg national minimum detection limit reference or the enterprise minimum detection limit reference standardized by the national reference. |
| Accuracy (HBeAg) | The relative deviation of the measurement results should be no more than 20% when using the national accuracy reference or the enterprise accuracy reference standardized by the national reference as a sample. |
| Positive Reference Concordance Rate (HBeAg) | Concordance rate (+/+) should be no less than 9/10 when testing 10 HBeAg national positive references or enterprise positive references standardized by national positive references. |
| Negative Reference Concordance Rate (HBeAg) | Concordance rate (-/-) should be 15/15 when testing 15 HBeAg national negative references or enterprise negative references standardized by national negative references. |
| Repeatability | The coefficient of variation (CV) should be no greater than 15% when repeatedly measuring 10 times with the HBeAg national precision reference or the enterprise precision reference standardized by the national reference. |
| Inter-batch Precision | The inter-batch coefficient of variation (CV) should be no greater than 15% when testing three batches of kits, each repeated 10 times, with the HBeAg national precision reference or the enterprise precision reference standardized by the national reference. |
| Stability | When stored at 4-30°C in a sealed aluminum foil bag, and tested with products within 1 month of the expiration date, the test results should meet the requirements for other performance indicators. |
Anti-Hepatitis B virus (HBeAg)
Hepatitis B e antigen (HBeAg) is a soluble protein produced during the replication of the Hepatitis B virus (HBV). It typically appears in the early stages of HBV infection. The presence of HBeAg usually indicates active viral replication and strong infectivity.
Technology Transfer
Technology transfer and customization
For research institutions and growing enterprises, especially those in the early stages of development, we offer a comprehensive suite of mature and stable production process technology transfer, along with relevant process documentation.
Additionally, we can tailor transformation production processes to align with diverse customer requirements and market needs.
This approach not only expedites the R&D and production process optimization timeline but also significantly reduces time and capital investment for our clients.
Expert lectures
The course will be led by seasoned industry experts, covering a range of topics including immunochromatography knowledge, theoretical explanations of process flows, and hands-on experimental operations. It will systematically address and analyze technical challenges faced by customers in their R&D and production processes, offering practical solutions.
Additionally, the course will feature demonstrations and practical operation sessions focused on immunochromatography equipment that is of particular interest to participants.
Process
The process unfolds as follows:
The customer outlines their requirements -> we collaborate to explore feasible solutions -> the customer settles the fee -> based on the provided solution, the customer either attends on-site training or receives remote guidance -> should production issues arise, we dispatch experts to the customer's site to offer on-site guidance and resolve the problems.
Research Outsourcing
We provide a variety of scientific and technical services, including laboratory equipment, experimental materials, data analysis and report writing, etc.
- Experimental Consumables and Chemical Reagents: We provide a comprehensive range of consumables and chemical reagents required for various experiments to meet the diverse needs of scientific research.
- Data Analysis: We are responsible for collecting and conducting in-depth analysis of experimental data, generating detailed reports to lay a solid foundation for the presentation of research findings.
- Technical Support: We offer comprehensive technical support to ensure the smooth progress of experiments, facilitating the successful conduct of research work.
- Customized Services: We possess the capability to tailor scientific and technological services to meet the specific needs and expectations of our clients, ensuring a high level of alignment and effectiveness in our offerings.
- One-Stop Services: We provide comprehensive one-stop scientific research services, including equipment rental and experimental material procurement, aiming to deliver a convenient and efficient user experience while streamlining the research process.
Process:
- Customer Submits Requirements: The customer clearly outlines their research or production needs, laying the foundation for subsequent services.
- Exploring Feasible Solutions: We engage in in-depth communication with the customer to jointly explore and formulate practical solutions, ensuring the forward-looking and operational nature of the service.
- Customer Pays Fees: Upon reaching a mutual agreement, the customer settles the relevant fees, providing assurance for the formal initiation of the service.
- Conducting Experiments or Data Characterization Analysis for the Customer: Based on the agreed-upon plan, we perform experimental operations or data characterization analysis for the customer, ensuring the process is professional and precise.
- Providing the Customer with a Detailed Experimental Report: Upon completion of the experiments or analysis, we deliver a comprehensive experimental report to the customer, offering robust support for their research or production decisions.
Semi-finished Products (large Packaging)
We can provide semi-finished (bulk packaged) reagents for quick assembly and application in your own country.
Advantages of Semi-Finished Reagents for Local Assembly:
- Rapid Market Entry: Quick assembly allows for swift deployment and faster market penetration.
- Compliance: Meets government self-production mandates and local regulatory requirements.
- Cost Efficiency: Reduces logistics and capital investment costs.
- Scalability: Flexible production adapts to market demand.
- Quality Assurance: Ensures consistent quality with local oversight.
- Competitive Edge: Combines global expertise with local production for a strategic advantage.
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