MB120: RNase A Solution
RNase A is commonly used in the processes of plasmid and genomic DNA purification and protein extraction, in addition to RNA sequence analysis and RNase protection assays.
Purity: >95% by reducing SDS-PAGE. Each lot of the RNase A (solution and powder) was tested to ensure the absence of protease, endonuclease, exonuclease, DNase, and DNA.
Specific activity: ≥ 60 Kunitz units/mg of protein.
The lowest RNase A solution price in the market.MB079: Recombinant Murine RNase Inhibitor (RI)
* High purity;
* Neither DNases nor RNases present;
* Compatible with RT-PCR and RT-qPCR.MB072: RNase-free and DNase-free Water
High quality, low priceMB127-5G: 5G RT Supermix for qPCR with gDNA Elimination Function
* The 5G RT supermix for qPCR with gDNA elimination function is suitable for two-step RT-qPCR detection, and compatible with dye-based and probe-based qPCR, enabling high-performance gene expression analysis.
* Simple and fast operation: one-step genome clearance and reverse transcription.
* Higher reverse transcription efficiency and higher cDNA yields from all regions of RNA transcripts: based on the more efficient 5G Reverse Transcriptase.
* Flexible choice of primers: Different types of reverse transcription primers can be used flexibly for different experimental designs.
* Excellent cDNA stability: complete deactivation of thermal DNase and long-term storage of cDNA.
MB127-4G: 4G RT Supermix for qPCR with gDNA Elimination Function
* The 4G RT supermix for qPCR with gDNA elimination function is suitable for two-step RT-qPCR detection, and compatible with dye-based and probe-based qPCR, enabling high-performance gene expression analysis.
* Based on the highly efficient 4G Reverse Transcriptase, the super temperature tolerance ensures that the complex secondary structure of RNA can be opened under high temperature conditions to obtain longer cDNA.
* Quick and complete removal of genome contamination by the 4 × gDNA Removing Buffer: to ensure more reliable follow-up results, and simplify the design of qPCR primers, without the need to design primers across introns.
* Different primers are selected for different downstream applications.BP002596-ENZ-611: Recombinant Human TatD DNase Domain Containing 3 (TATDN3) Enzyme
Source: E. coli-derived.
Purity: > 90% as determined by SDS-PAGE.