The genesig® Dengue, Zika and Chikungunya Virus Multiplex kit is designed for the detection and differentiation of Dengue virus, Zika virus (ZIKV) and Chikungunya virus (CHIKV) only. Individual tests have been designed in the conserved regions of each virus such that all isolates and subtypes will be detected simultaneously in the same test. The Dengue component of the test will detect subtypes 1, 2, 3 and 4 but will not differentiate between them. A positive Dengue test results indicates that the sample has either one of these four subtypes.
The primers and probe sequences in this kit have 100% homology with a broad range of clinically relevant reference sequences based on a comprehensive bioinformatics analysis. They therefore have a very broad quantification profile.
Exceptional value for money
Rapid detection of all clinically relevant subtypes
Positive copy number standard curve for quantification
Highly specific detection profile
High priming efficiency
Broad dynamic detection range (>6 logs)
Sensitive to < 100 copies of target
Accurate controls to confirm findings
150 reactions
This product provides fast and easy methods for purification of total DNA for reliable PCR and Southern blotting. Total DNA(e.g., genomic, viral, mitochondrial) can be purified from small volume of blood, tissue and dry blood spots.
Specifications
Features | Specifications |
Main Functions | Isolation total DNA from 1-10μl blood, <10mg tissue, urine, blood stain, seminal stain |
Applications | PCR, southern bolt and virus detection, etc. |
Purification method | Mini spin column |
Purification technology | Silica technology |
Process method | Manual (centrifugation or vacuum) |
Sample type | Animal tissues, blood stain, urine, seminal stain and various forensic samples |
Sample amount | Blood:1-100μl, Tissue:<10mg |
Elution volume | |
Time per run | |
Liquid carrying volume per column | |
Binding yield of column |
This product is based on silica Column purification. The sample is lysed and digested with lysate and protease, DNA is released into the lysate. Transfer to an adsorption column. Nucleic acid is adsorbed on the membrane, while protein is not adsorbed and is removed with filtration. After washing proteins and other impurities, nucleic acid was finally eluted with low-salt buffer (10mmTris, pH9.0, 0.5mm EDTA).
Kit Contents
Contents | D312502 | D312503 |
Purification Times | 50 Preps | 250 Preps |
Buffer ATL | 15 ml | 60 ml |
Buffer AL | 15 ml | 60 ml |
Buffer GW1* | 22 ml | 66 ml |
Buffer GW2* | 20 ml | 2 x 50 ml |
Carrier RNA | 310 μg | 2 x 310 µg |
Proteinase K | 24 mg | 120 mg |
Protease Dissolve Buffer | 1.8 ml | 10 ml |
Buffer AE | 15 ml | 60 ml |
HiPure DNA Mini Columns I | 50 | 2 x 125 |
2 ml Collection Tubes | 100 | 5 x 100 |
Storage and Stability
Carrier RNA and Proteinase K should be stored at 2–8°C upon arrival. However, short-term storage (up to 12 weeks) at room temperature (15–25°C) does not affect its performance. The remaining kit components can be stored dry at room temperature (15–25°C) and are stable for at least 18 months under theseconditions.
Experiment Data
This product provides fast and easy methods for purification of total DNA for reliable PCR and Southern blotting. Total DNA(e.g., genomic, viral, mitochondrial) can be purified from small volume of blood, tissue and dry blood spots.
DBCO-PEG4-Maleimide is PEG linker containing a maleimide group and a DBCO moiety. The hydrophilic PEG spacer arm improves solubility in aqueous buffers. Maleimide group specifically and efficiently reacts with thiols to form stable thioether bonds. The low mass weight will add minimal spacer to modified molecules and will enable simple and efficient incorporation of DBCO moiety onto cysteine-containing peptides or other thiol-containing biomolecules. DBCO is commonly used for copper-free Click Chemistry reactions. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
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Tel : 081-875-1869 , 02-328-7179
Email : hej@a3p-scientific.com
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