Category: COVID-19

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  • Categories: Nucleic Acid Purification products
Reference: D6293-00

Modified from the E.Z.N.A.® Cycle Pure Kit, the E.Z.N.A.® MicroElute Cycle Pure Kit is specially designed to purify PCR samples with a small elution volume of 10-15 µL. Highly concentrated DNA eluates are ready to use in all subsequent applications.

Reference: D6293-01

Modified from the E.Z.N.A.® Cycle Pure Kit, the E.Z.N.A.® MicroElute Cycle Pure Kit is specially designed to purify PCR samples with a small elution volume of 10-15 µL. Highly concentrated DNA eluates are ready to use in all subsequent applications.

Reference: D6293-02

Modified from the E.Z.N.A.® Cycle Pure Kit, the E.Z.N.A.® MicroElute Cycle Pure Kit is specially designed to purify PCR samples with a small elution volume of 10-15 µL. Highly concentrated DNA eluates are ready to use in all subsequent applications.

Reference: D6294-00

By using a unique MicroElute spin column, the E.Z.N.A.® MicroElute Gel Extraction Kit is designed for the purification of DNA fragments from agarose gels with a small elution volume of 10-15 µL.

Reference: D6294-01

By using a unique MicroElute spin column, the E.Z.N.A.® MicroElute Gel Extraction Kit is designed for the purification of DNA fragments from agarose gels with a small elution volume of 10-15 µL.

Reference: D6294-02

By using a unique MicroElute spin column, the E.Z.N.A.® MicroElute Gel Extraction Kit is designed for the purification of DNA fragments from agarose gels with a small elution volume of 10-15 µL.

Reference: D6492-00

The E.Z.N.A.® Cycle-Pure Kit is designed for the rapid purification of single or double-stranded DNA from PCR and other enzymatic reactions. The system follows a bind-wash-elute procedure and completely removes primers, nucleotides enzymes, salts, and other impurities from a DNA sample. This convenient spin-column format eliminates the need for expensive resins or toxic organic compounds such as phenol and chloroform, thereby making it possible to process multiple samples in parallel. Purified DNA can be used in T-A ligations, sequencing, restriction enzyme digestion, and various other labeling reactions.

Reference: D6492-01

The E.Z.N.A.® Cycle-Pure Kit is designed for the rapid purification of single or double-stranded DNA from PCR and other enzymatic reactions. The system follows a bind-wash-elute procedure and completely removes primers, nucleotides enzymes, salts, and other impurities from a DNA sample. This convenient spin-column format eliminates the need for expensive resins or toxic organic compounds such as phenol and chloroform, thereby making it possible to process multiple samples in parallel. Purified DNA can be used in T-A ligations, sequencing, restriction enzyme digestion, and various other labeling reactions.

Reference: D6492-02

The E.Z.N.A.® Cycle-Pure Kit is designed for the rapid purification of single or double-stranded DNA from PCR and other enzymatic reactions. The system follows a bind-wash-elute procedure and completely removes primers, nucleotides enzymes, salts, and other impurities from a DNA sample. This convenient spin-column format eliminates the need for expensive resins or toxic organic compounds such as phenol and chloroform, thereby making it possible to process multiple samples in parallel. Purified DNA can be used in T-A ligations, sequencing, restriction enzyme digestion, and various other labeling reactions.

Reference: D6926-00

The E.Z.N.A.® Endo-Free Plasmid DNA Maxi Kit provides an efficient method for the large-scale isolation of low-endotoxin plasmid DNA. The system utilizes Lysate Clearance Filter Syringes instead of centrifugation to rapidly clear bacterial lysates post-alkaline lysis. Following lysate clearance, endotoxins are removed, and the protocol follows a simple bind-wash-elute procedure to deliver high-quality plasmid DNA. The yields vary according to plasmid copy number, E. coli strain, and growth conditions. 50-200 mL of bacterial cultures in LB medium typically produces 0.6-1.2 mg of high copy number plasmid DNA. Up to 500 mL of culture may be processed when working with low copy number plasmid. The system uses centrifugation or vacuum technology for plasmid purification and eliminates the time-consuming gravity-flow columns that require alcohol precipitation. Purified plasmid DNA is suitable for sensitive downstream applications such as transfection of mammalian cells, cloning, automated fluorescent DNA sequencing (typical reads exceed 800 bp), next-generation sequencing, restriction enzyme digestion, ligation, PCR, in vitro transcription, transformation, etc.

Reference: D6926-01

The E.Z.N.A.® Endo-Free Plasmid DNA Maxi Kit provides an efficient method for the large-scale isolation of low-endotoxin plasmid DNA. The system utilizes Lysate Clearance Filter Syringes instead of centrifugation to rapidly clear bacterial lysates post-alkaline lysis. Following lysate clearance, endotoxins are removed, and the protocol follows a simple bind-wash-elute procedure to deliver high-quality plasmid DNA. The yields vary according to plasmid copy number, E. coli strain, and growth conditions. 50-200 mL of bacterial cultures in LB medium typically produces 0.6-1.2 mg of high copy number plasmid DNA. Up to 500 mL of culture may be processed when working with low copy number plasmid. The system uses centrifugation or vacuum technology for plasmid purification and eliminates the time-consuming gravity-flow columns that require alcohol precipitation. Purified plasmid DNA is suitable for sensitive downstream applications such as transfection of mammalian cells, cloning, automated fluorescent DNA sequencing (typical reads exceed 800 bp), next-generation sequencing, restriction enzyme digestion, ligation, PCR, in vitro transcription, transformation, etc.

Reference: D6926-03

The E.Z.N.A.® Endo-Free Plasmid DNA Maxi Kit provides an efficient method for the large-scale isolation of low-endotoxin plasmid DNA. The system utilizes Lysate Clearance Filter Syringes instead of centrifugation to rapidly clear bacterial lysates post-alkaline lysis. Following lysate clearance, endotoxins are removed, and the protocol follows a simple bind-wash-elute procedure to deliver high-quality plasmid DNA. The yields vary according to plasmid copy number, E. coli strain, and growth conditions. 50-200 mL of bacterial cultures in LB medium typically produces 0.6-1.2 mg of high copy number plasmid DNA. Up to 500 mL of culture may be processed when working with low copy number plasmid. The system uses centrifugation or vacuum technology for plasmid purification and eliminates the time-consuming gravity-flow columns that require alcohol precipitation. Purified plasmid DNA is suitable for sensitive downstream applications such as transfection of mammalian cells, cloning, automated fluorescent DNA sequencing (typical reads exceed 800 bp), next-generation sequencing, restriction enzyme digestion, ligation, PCR, in vitro transcription, transformation, etc.