Colourless Appearance RNase Inhibitor Murine R4001 20000U
Product Details:
Place of Origin: | China |
Brand Name: | GDSBio |
Certification: | / |
Model Number: | R4001 |
Payment & Shipping Terms:
Minimum Order Quantity: | 1 bag |
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Packaging Details: | small package or bulk distribute or OEM |
Delivery Time: | 8work days |
Payment Terms: | L/C, D/A, D/P, T/T, Western Union, MoneyGram |
Supply Ability: | 100 Bag/Bags Per Day |
Detail Information |
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Cat. No.: | R4001 | Concentration: | 20,000U |
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Appearance: | Colourless | Group: | Reverse Transcriptase PCR Reagents |
Activity: | Pass | Amplification Capability: | / |
Logo Printing: | With Logo Printing | Transport Package: | Packing |
Production Capacity: | 100 Bag/Bags Per Day | Storage Conditions: | Store At -20°C |
High Light: | Colourless Appearance RNase Inhibitor Murine,20000U RNase Inhibitor Murine,20000U rnase inhibitor chemical |
Product Description
RNase Inhibitor Murine R4001 20,000U
RNase Inhibitor (Murine)
For research use only
Components
Component | R4001 (20,000 U) |
RNase Inhibitor (Murine) (40 U/μl) |
500 μl |
Storage
This reagent should be kept at -20°C.
Description
RNase Inhibitor (Murine) is a recombinant murine source RNase inhibitor expressed in the soluble form in E. coli. It can inhibit a wide range of RNases (RNase A, B, C). It has been tested by RT-PCR, RT-qPCR and is compatible with various reverse transcriptase and DNA polymerases. Compared with human source RNase inhibitors, murine source RNase inhibitors do not contain two of the very oxidation-sensitive cysteines of human proteins, so they have higher antioxidant activity and are more suitable for experiments with high DTT sensitivity, such as qPCR.
Unit Definition
The amount of enzyme required to inhibit 50% of 5 ng RNase A activity was defined as 1 unit of activity (U). The activity of RNase A is quantitatively obtained by hydrolyzing 2 ', 3' -CMP to generate 3 '-CMP.
Quality Control
Exonuclease residue detection: 200 U of this product and 0.6 μg of λ-Hind III were incubated at 37°C for 16 h, and the DNA bands did not change after electrophoresis.
Detection of endonuclease residue: 200 U of this product and 0.6 μg of Supercoiled pBR322 DNA were incubated at 37°C for 4 h, and the DNA bands did not change after electrophoresis.
E.coli DNA residue detection: the nucleic acid residue in 200 U of this product was detected by E. coli gDNA-specific TaqMan qPCR, and the residue of E. coli genome was less than 10 copies.
Application
1. Synthesis of the first strand of cDNA
2. Polysome isolation
3. In vitro transcription
4. No cell translation system in vitro
Matters Needing Attention
1. RNase activity was inhibited by a wide range of pH values, with the maximum activity at pH 7 ~ 8.
2. Foaming or vigorous stirring (Vortex, etc.) can cause inactivation.
3. RNase H activity will not be inhibited.
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