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Polaris® qPCR Buffer 2.5x, IVD
Polaris® qPCR Buffer 2.5x, IVD, is a validated Class A IVD reagent, designed to enhance the reliability and accuracy of diagnostic PCR, multiplex PCR and quantitative real-time PCR (qPCR) that demand rapid amplification without compromising specificity or sensitivity. The buffer ensures optimal conditions for PCR reactions by maintaining a stable pH and providing essential ions and cofactors that enhance enzyme efficiency.
Polaris® qPCR Buffer 2.5x, IVD, designed for in vitro diagnostic (IVD) applications, is a highly optimized buffer solution specifically developed to enhance the performance, reliability, and accuracy of molecular diagnostics. This buffer contains the necessary components, additives, and stabilizers to promote the activity of polymerases and their accessory proteins during qPCR. The Polaris® qPCR Buffer 2.5x, IVD, ensures optimal conditions for PCR reactions by maintaining a stable pH and providing essential ions and cofactors that enhance enzyme efficiency. This critical feature significantly reduces the likelihood of errors during the amplification process and enhances the yield and specificity of the desired PCR products. Polaris® qPCR Buffer 2.5x, IVD, improves the reliability and accuracy of diagnostic PCR, multiplex PCR and quantitative real-time PCR (qPCR) that demand rapid amplification without compromising specificity or sensitivity. Offered in a 2.5x concentration, this buffer is ideal for use in the concentrated bulk production of qPCR reagents. It is specially formulated to promote highly efficient qPCR, stabilize enzymes, and enhance overall enzyme activity, facilitating its integration into various diagnostic workflows.
Polaris® qPCR Buffer 2.5x, IVD, is produced under a rigorous quality management system according to global standards for medical devices and IVD manufacturing, including stringent quality assurance, full traceability from production, and reliability in its diagnostic applications. The efficacy of Polaris® qPCR Buffer 2.5x, IVD, is especially relevant in the field of molecular diagnostics, as evidenced in this instruction manual through extensive validation for detecting a wide range of viral and bacterial pathogens, including methicillin-resistant Staphylococcus aureus (MRSA), and 14 high-risk types of Human Papillomavirus (HPV) in human clinical specimens. The comprehensive validation of Polaris® qPCR Buffer 2.5x, IVD, across diverse clinical matrices, establishes it as a validated Class A IVD reagent for molecular diagnostics.
Features:
Intended Use:
Polaris® qPCR Buffer 2.5x, IVD, is a validated Class A IVD reagent, intended for professional use in the real-time PCR detection of viral, bacterial and fungal DNA in swab samples collected from patients. A positive result indicates the presence of pathogen nucleic acids but a clinical correlation with patient history and other diagnostic information is necessary to determine the patient's infection status. Negative results do not preclude microbial infection and should not be used as the sole basis for patient management decisions. Thus, the results obtained with tests using this product should be interpreted in conjunction with other clinical and laboratory findings. This IVD reagent is intended for use by properly licensed laboratory professionals. The performance characteristics of this product were established based on the detection of two highly relevant human pathogens, MRSA and HPV. Laboratories should validate performance for other targets according to local regulations and guidelines. Polaris® qPCR Buffer 2.5x, IVD, supports robust, sensitive, and specific diagnostic assays. This flexibility, when combined with the ability to customize assays with additional separate components, establishes Polaris® qPCR Buffer 2.5x, IVD, as the go-to buffer for diagnostic laboratories, PCR kit manufacturers and molecular testing facilities focused on crafting and deploying superior molecular diagnostics. The extensive validation and versatility of this product underscores Polaris® qPCR Buffer 2.5x, IVD, as a robust class A diagnostic reagent, capable of accommodating varied diagnostic demands and capable of delivering reliable results across different biological matrices and testing conditions.
In case the IFU is not available in your official country language, please contact us – info@NZYtech.com so that we can proceed with the translation. Please see languages available below.
Find the IFU for your product batch
Polaris® qPCR Buffer 2.5x, IVD, is produced under a rigorous quality management system according to global standards for medical devices and IVD manufacturing, including stringent quality assurance, full traceability from production, and reliability in its diagnostic applications. The efficacy of Polaris® qPCR Buffer 2.5x, IVD, is especially relevant in the field of molecular diagnostics, as evidenced in this instruction manual through extensive validation for detecting a wide range of viral and bacterial pathogens, including methicillin-resistant Staphylococcus aureus (MRSA), and 14 high-risk types of Human Papillomavirus (HPV) in human clinical specimens. The comprehensive validation of Polaris® qPCR Buffer 2.5x, IVD, across diverse clinical matrices, establishes it as a validated Class A IVD reagent for molecular diagnostics.
Features:
- Sensitivity and Specificity
- Accuracy and Reproducibility
- Stability and Robustness
Intended Use:
Polaris® qPCR Buffer 2.5x, IVD, is a validated Class A IVD reagent, intended for professional use in the real-time PCR detection of viral, bacterial and fungal DNA in swab samples collected from patients. A positive result indicates the presence of pathogen nucleic acids but a clinical correlation with patient history and other diagnostic information is necessary to determine the patient's infection status. Negative results do not preclude microbial infection and should not be used as the sole basis for patient management decisions. Thus, the results obtained with tests using this product should be interpreted in conjunction with other clinical and laboratory findings. This IVD reagent is intended for use by properly licensed laboratory professionals. The performance characteristics of this product were established based on the detection of two highly relevant human pathogens, MRSA and HPV. Laboratories should validate performance for other targets according to local regulations and guidelines. Polaris® qPCR Buffer 2.5x, IVD, supports robust, sensitive, and specific diagnostic assays. This flexibility, when combined with the ability to customize assays with additional separate components, establishes Polaris® qPCR Buffer 2.5x, IVD, as the go-to buffer for diagnostic laboratories, PCR kit manufacturers and molecular testing facilities focused on crafting and deploying superior molecular diagnostics. The extensive validation and versatility of this product underscores Polaris® qPCR Buffer 2.5x, IVD, as a robust class A diagnostic reagent, capable of accommodating varied diagnostic demands and capable of delivering reliable results across different biological matrices and testing conditions.
In case the IFU is not available in your official country language, please contact us – info@NZYtech.com so that we can proceed with the translation. Please see languages available below.
Find the IFU for your product batch
Shipping Conditions | Room Temperature | Storage Conditions | -85 °C to -15 °C | Format | Liquid | Product Category | Polaris® qPCR | Marking | CE-IVD | Internal Control | No | Features | Ultra-pure grade |
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qPCR Buffer 2.5x
Shipping Conditions | Room Temperature | Storage Conditions | -85 °C to -15 °C | Format | Liquid | Product Category | Polaris® qPCR | Marking | CE-IVD | Internal Control | No | Features | Ultra-pure grade |
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Shipping Conditions | Room Temperature | Storage Conditions | -85 °C to -15 °C | Format | Liquid | Product Category | Polaris® qPCR | Marking | CE-IVD | Internal Control | No | Features | Ultra-pure grade |
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Certificate of Analysis