T7 High Efficiency Transcription Kit
Cat.No:PC4120 Solarbio
Storage:-20℃
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T7 High Efficiency Transcription KitStorage:-20℃
Qty:
Size:
Storage | -20℃ |
Note | 1. When using PCR product template or plasmid template, it is necessary to ensure that there is no ethanol residue in the template. Therefore, when dissolving DNA precipitation, it is necessary to open the lid to completely volatilize ethanol, which can be carried out in a clean workbench. 2. The reaction of in vitro transcription is highly sensitive to RNase, and the reaction system should be strictly careful not to mix with RNase. Experimental equipment such as pipette head and EP tube should strictly use RNASE-free supplies. The preparation of the system is as far as possible in an enzyme-free environment, which can be done using a clean table after cleaning, and the synthesized RNA is also as far as possible to avoid opening the lid outside the clean table to avoid RNase contamination. 3. When preparing the system, please add samples in strict accordance with the adding sequence in the instructions. 10×Transcription Buffer needs to be used after restoration to room temperature, and DNA is prone to co-precipitation with spermidine at low temperature, which will affect the transcription output. |
Unit | Box |
Specification | 50T |
The kit has optimized a series of transcription reaction systems for different templates and different nucleotide types, and users can efficiently obtain a large number of RNA products from DNA through this product. The kit uses RNA polymerase that recognizes T7 promoter, takes plasmid or PCR product containing T7 promoter sequence as template, uses natural nucleotide or modified nucleotide as substrate, and can obtain high-yield single-stranded RNA through short in vitro transcription. At the same time, complete mRNA with hat structure can be transcribed by this kit by adding Cap0 or Cap1 and other hat structure or hat structure analogues to the substrate. This kit is recommended to use 20μL in vitro transcription system, input 1μg plasmid template or equivalent PCR product template, use natural or modified nucleotides, in vitro transcription yield of more than 200μg, through process design and optimization, can be used for the amplification of gram level RNA production. The RNA synthesized by transcription can be used to analyze the properties and structure of RNA. Single-stranded RNA without hat structure is easy to degrade, so we suggest downstream processing according to project requirements, and cyclic RNA should be processed downstream as soon as possible. Linear RNA can be capped by vaccinia virus capping system and dioxymethyltransferase. The use of cotranscription capped mRNA can be directly used in the study of mRNA function.
Remark:These protocols are for reference only. Solarbio does not independently validate these methods.
Note:
1. The products are all for scientific research use only. Do not use it for medical, clinical diagnosis or treatment, food and cosmetics, etc. Do not store them in ordinary residential areas.
2. For your safety and health, please wear laboratory clothes, disposable gloves and masks.
3. The experimental results may be affected by many factors, after-sale service is limited to the product itself and does not involve other compensation.
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