Difference between revisions of "Part:BBa K4712086"
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<partinfo>BBa_K4712086 parameters</partinfo> | <partinfo>BBa_K4712086 parameters</partinfo> | ||
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+ | |||
+ | <h1> Protocol | ||
+ | |||
+ | Apparatus: | ||
+ | Thermal Cycler, Centrifuge, Fluorescence Quantitative PCR Instrument (Ya Rui), 2mL reaction tube, Pipette and Pipette Tip | ||
+ | |||
+ | Materials: | ||
+ | 1. DNA Isothermal Amplification Kit (EZ-Life Biotechnology) | ||
+ | 2. ddH2O | ||
+ | 3. Thermostatic amplification specific primers: | ||
+ | INFB-F1、 INFB-R1 | ||
+ | INFB-F2、 INFB-R2 | ||
+ | INFB-F3、 INFB-R3 | ||
+ | INFB-F4、 INFB-R4 | ||
+ | INFB-F5、 INFB-R5 | ||
+ | H1N1-F6、H1N1-R6 | ||
+ | H1N1-F7、H1N1-R7 | ||
+ | H1N1-F8、H1N1-R8 | ||
+ | 4. DL500 marker | ||
+ | 5. Test sample: DNA Template(pUC57-M1)Concentration:1000cps/μL | ||
+ | Storage: -20°C | ||
+ | |||
+ | Methods: | ||
+ | 1. For a 20μL reaction system: | ||
+ | <table> | ||
+ | <thead> | ||
+ | <tr> | ||
+ | <th>Reagent</th> | ||
+ | <th>Stock Concentration</th> | ||
+ | <th>Volume Added(μL)</th> | ||
+ | </tr> | ||
+ | </thead> | ||
+ | <tbody> | ||
+ | <tr> | ||
+ | <td>Forward Primer</td> | ||
+ | <td>10μM</td> | ||
+ | <td>1</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Reverse Primer</td> | ||
+ | <td>10μM</td> | ||
+ | <td>1</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Rehydration Buffer (2X)</td> | ||
+ | <td></td> | ||
+ | <td>10</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>DNA Template</td> | ||
+ | <td>10nM/L</td> | ||
+ | <td>2</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>H2O</td> | ||
+ | <td></td> | ||
+ | <td>To 18</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Starter (10X)</td> | ||
+ | <td></td> | ||
+ | <td>2</td> | ||
+ | </tr> | ||
+ | </tbody> | ||
+ | </table> | ||
+ | 2. Gently tap multiple times to mix the ingredient, and then centrifuge briefly (mix gently, avoiding vigorous shaking or vortexing). | ||
+ | 3. Incubate at 37 ℃ for 20 minutes. | ||
+ | 4. After heating at 65 ℃ for 10 minutes, the adhesive will run off. |
Revision as of 11:55, 12 October 2023
Cd-F1
The primers were designed using NCBI BLAST and SanpGene to achieve efficient and specific amplification. This primer in RPA serves as the initial binding point for the amplification process, ensuring the specificity of the reaction by targeting the desired Corynebacterium diphtheria DNA or RNA sequences. The primers provided data for mathematical modeling for further primer design.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]