Customization: | Available |
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Transport Package: | Box |
Specification: | 200 Preps/Kit |
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Magen's Nucleic Acid Isolation &Purification Kits Germany in-Vitro Diagnostic registered (98/79/EC) Chinese in vitro diagnostic Reagent Glass I, 20150062) |
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Function Name | Cat.No. | Quality (Preps) |
Price |
Nucleic Acid Type | Method | Sample | Applicaton |
HiPure Universal DNA Kit | IVD3018 | 100 | genomic DNA | Silica-gel Column |
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PCR, Real time PCR NGS Library prepare |
|
HiPure Circulating DNA Kit | IVD3182 | 50 |
Circulating DNA | 1~5 ml Plasma, Serum, cerebral effusion, ascites, cell culture supernatants. | PCR, Real time PCR NGS Library prepare |
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HiPure Viral DNA/RNA Kit | IVD4173 | 100 | Viral Nucleic Acid |
~200ul Plasma, Serum, Swab Soak, Tissue homogenate superatant, other body fluids | Real Time PCR PCR |
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HiPure Viral RNA Kit | IVD4175 | 100 | Viral RNA | ~200ul Plasma, Serum, Swab Soak, Tissue homogenate superatant , other body fluids | Real time PCR PCR |
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MagPure Universal DNA Kit | IVD3102 | 200 | genomic DNA | Magnetic Particles |
|
PCR, Real time PCR NGS Library prepare |
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MagPure Viral DNA/RNA Kit | IVD5412 (Bottle package) | 200 | Viral Nucleic Acid |
~200ul Plasma, Serum, Swab Soak, Tissue homogenate superatant, other body fluids | Real Time PCR PCR |
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IVD5412-F-96 (Precast for kingFisher Flex) |
96 | ||||||
IVD5412-TL-96 (Precast for 32 channel Machine) |
96 | ||||||
MagPure Stool DNA Kit | D6364-400 | 400 | Stool DNA | Isolation Total DNA include microbial DNA from ~150mg Stool Samples. | PCR, Real time PCR NGS Library prepare |
Product Name MagPure Viral Nucleic Acid Isolation Kit
Cat. No. & SpecificationsIVD5412, 96 Preps/Kit; 200 Preps/Kit
Intended Use
This product is suitable for extracting total viral nucleic acid from cell-free/low-content cell biological samples such as body fluids, serums, plasma, soaking solutions, tissue homogenate supernatant, and culture supernatant. The Purified DNA/RNA is used for RT-PCR and PCR detection.
Principle
This product is based on the purification method of high binding magnetic particles. The sample is lysed and digested under the action of lysate and Protease. DNA/RNA is released into the lysate. After adding magnetic particles and binding solution, DNA/RNA will be adsorbed on the surface of magnetic particles, and impurities such as proteins will be removed without adsorption. The adsorbed particles were washed with washing solution to remove proteins and impurities, washed with ethanol to remove salts, and finally DNA/RNA was eluted by Nuclease Free Water.
Main Composition
96 preps | 200 preps | Contents | |
MagPure Particles N | 2.5 ml | 5 ml | Magnetic Bead/NaCl/NaN3 |
PK/Carrier RNA | 25 mg | 50 mg | Protease |
Protease Dissolve Buffer Blue | 5 ml | 5 ml | Glycerol/CaCl2/Tris |
Buffer MLB | 60 ml | 120 ml | Guanidine Salt/Isopropanol/EDTA |
Buffer MW1 | 26 ml | 53 ml | Guanidine Salt/Tris/EDTA |
Nuclease Free Water | 15 ml | 30 ml | 10mm Tris, pH8.0 |
Name of the Plate | Pre-loaded reagents | Addition before use |
Sample plate | 500µl Buffer MLB 20µl MagPure Particle MPN |
200µl sample 10µl PK/Carrier RNA |
Wash Plate 1 | 500µl Buffer MW1, Put in 96 magnetic Tip | |
Wash Plate 2 | 500µl 80% ethanol | |
Wash Plate 3 | 500µl 80% ethanol | |
Elution plate | 50~100µl Nuclease Free Water |