DBCO-PEG2-acid is an analog of DBCO-Acid with PEG linker and a DBCO group. The DBCO groups is commonly used for copper-free Click Chemistry reactions due to its strain promoted high energy. The hydrophilic PEG chain allows for increased water solubility. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
DBCO-PEG2-acid is an analog of DBCO-Acid with PEG linker and a DBCO group. The DBCO groups is commonly used for copper-free Click Chemistry reactions due to its strain promoted high energy. The hydrophilic PEG chain allows for increased water solubility. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
DD5 Low Speed 5000rpm Swing rotor 4x800ml lab Centrifuge Adapters for 5/10/15/50ml tubes.
DD5 Low Speed Large Capacity Centrifuge Application:
DD5 Lab centrifuge widely used in the fields of pharmaceutical factory and laboratory, can hold swing out rotors and angle rotors both.
DD5 Low Speed Large Capacity Centrifuge Features:
1. Brushless frequency motor which in great torque, free maintenance, no powder pollution, quick in speed up and down.
2. Digital display which indicates the program, speed, time, RCF and temperature.
3. Micro computer control, there are 10 kinds of program and 10 kinds of acceleration/deceleration for your choice.
4. There are kinds of rotors for your choice.
5. Electric lid lock, compact design, super speed and imbalance protection.
6. The centrifuge body is made of high-quality steel, safe and reliable.
DD5 Low Speed Laboratory Centrifuge Technical Parameters:
| Max. Speed | 5000rpm |
| Max.RCF | 4730xg |
| Max.Capacity | 4x800ml |
| Timer | 0~99mins |
| RPM/RCF Convert | Yes |
| Noise(DB) | ≤58 |
| Acc/Dec | 10 Rates |
| Speed Accuracy | ±20rpm |
| Voltage(V/HZ) | AC 220V/110V 50HZ/60HZ |
| Dimension(LxWxH mm) | 720x540x830 |
| Net Weight(Kg) | 108kg |
| Certificates | CE,ISO |
| Warranty | 1 Year |
DD5 Low Speed Laboratory Centrifuge Matched Rotors:
| Order No. | Rotor type | Max.Speed (rpm) | Max.Volume (ml) | Max.RCF (xg) |
| No30671 | Swing out rotor | 4,000 | 4x800ml(round cup) | 3,450 |
| No30679 | Swing out rotor | 4,000 | 4x500ml(square cup) | 3,450 |
| No30696 | Swing out rotor | 4,000 | 4x500ml(round cup) | 3,530 |
| No31377 | Swing out rotor | 5,000 | 4x50ml | 4,730 |
| 4x100ml | 4,730 | |||
| No30592 | Swing out rotor | 4,000 | 4x30x7ml | 3,140 |
| 4x40x7ml | 3,270 | |||
| 4x18x10ml | 3,140 | |||
| No31491 | Mircoplater rotor | 4,000 | 2x4x96well | 2,910 |
| No31494 | Microplater rotor | 4,000 | 4x4x96well | 2,940 |
| No30627 | Angle rotor | 5,000 | 30x15ml | 3,830 |
| No30641 | Angle rotor | 5,000 | 12x50ml | 3,860 |
| No30642 | Angle rotor | 4,000 | 24x50ml | 2,970 |
| No30614 | Angle rotor | 5,000 | 6x100ml | 3,130 |
| No30643 | Angle rotor | 4,000 | 12x100ml | 2,970 |
The Corners of our Company____________________________________
Description
The SMOChem™ Deoxynucleotide (dNTP) Mix is an aqueous solution that contains an equimolar solution of ultrapure dATP, dCTP, dGTP and dTTP, each at a concentration of 25 mM at pH 8.5. The dNTP Mix is designed for many different molecular biology applications that involved in DNA synthesis or labeling, such as PCR, real-time PCR, DNA sequencing, reverse transcription, primer extension, and etc. The dNTP Mix is free of exo-deoxyribonuclease and endo-deoxyribonuclease as well as ribonuclease activity. The dNTP Mix offers the possibility to reduce the number of pipetting steps and the risk of reaction set up errors.
Features
Applications
Storage
-20°C for 36 months
The SMOChem™ Deoxynucleotide (dNTP) Mix is an aqueous solution that contains an equimolar solution of ultrapure dATP, dCTP, dGTP and dTTP, each at a concentration of 25 mM at pH 8.5. The dNTP Mix is designed for many different molecular biology applications that involved in DNA synthesis or labeling, such as PCR, real-time PCR, DNA sequencing, reverse transcription, primer extension, and etc. The dNTP Mix is free of exo-deoxyribonuclease and endo-deoxyribonuclease as well as ribonuclease activity. The dNTP Mix offers the possibility to reduce the number of pipetting steps and the risk of reaction set up errors.
HL-dsDNase is especially developed to remove contaminating genomic DNA from RNA preparations. Figure 1 shows that HL-dsDNase can reduce 50 ng of human gDNA to levels non-detectable by qPCR. In figure 2, a human total RNA sample was treated with HL-dsDNase and analysed on the Bio-Rad Experion™ System. The results indicate that HL-dsDNase has minimal impact on RNA quality and quantity.
HL-dsDNase is an engineered version of dsDNase that is rapidly and completely inactivated by incubation for 5 minutes at 58°C with 1 mM DTT at pH 8.0 or above. Chemical inactivation in downstream compatible RT or PCR buffers allows milder heat inactivation and, in some cases, skipping heat inactivation altogether. This makes HL-dsDNase very useful for removal of DNA from RNA preparations since the enzyme may be inactivated using various strategies with reduced risk of auto-degradation of RNA in the presence of magnesium, making HL-dsDNase an ideal enzyme when working with small volumens of RNA.
HL-dsDNase is also an excellent choice for removal of unwanted external DNA from samples prior to analysis of nucleic acids protected by biological membranes, e.g., bacteria, viruses, and sperm. Especially if using downstream analysis methods that might be affected by host cell DNA, as metagenomic sequencing and STR-profiling. The easy inactivation of HL-dsDNase makes it a fast and efficient alternative to methods as differential extraction, where sample material is often lost.
HL-dsDNase is especially developed to remove contaminating genomic DNA from RNA preparations. Figure 1 shows that HL-dsDNase can reduce 50 ng of human gDNA to levels non-detectable by qPCR. In figure 2, a human total RNA sample was treated with HL-dsDNase and analysed on the Bio-Rad Experion™ System. The results indicate that HL-dsDNase has minimal impact on RNA quality and quantity.
