E.Z.N.A.® SP Plant DNA Kit Reference: D5511-02 The E.Z.N.A.® SP Plant DNA Kit is specially designed for the rapid and reliable isolation of high-quality total cellular DNA from a variety of plant species and tissues. Up to 100 mg of fresh sample or 30 mg of dry sample can be processed in less than 40 minutes. The optimized procedure incorporates the homogenizer spin column, a unique filter filtration and homogenization column that can efficiently remove cell debris and improve the sample handling following the sample lysis. Purified DNA is suitable for most downstream applications to include PCR, restriction enzyme digestion, and hybridization techniques.
DNase I , RNase-free Reference: EN401-01 DNase I (deoxyribonuclease I), that is, Deoxyribonuclease I, is an endodeoxyribonuclease that can digest single-stranded or double-stranded DNA. It recognizes and cleaves phosphodiester bonds to produce a 5'-end phosphate group Group, 3'-end hydroxyl monodeoxynucleotide or single-stranded or double-stranded oligodeoxynucleotide. The activity of DNase I depends on Ca2+ and can be activated by divalent metal ions Mg2+, Mn2+, etc. It exists in Mg2+ In the case of Mn2+, the enzyme can randomly recognize and cut any site on any strand of double-stranded DNA; and in the presence of Mn2+, it can recognize and cut almost the same site on both strands of DNA, resulting in blunt ends or There are sticky-end DNA fragments with 1-2 nucleotides protruding. This product has undergone strict quality control and is suitable for RNA extraction, in vitro transcription, DNA removal in RT-PCR experiments, DNase I footprinting, nick translatioin, DNA random fragment library construction and other molecular biology experiment. Application: High activity Very low RNase residue Good stability
E.Z.N.A.® Water DNA Kit Reference: D5525-00 The E.Z.N.A.® Water DNA Kit is formulated to isolate high-purity cellular DNA from water samples typically containing humic acid and inhibitors of PCR. This kit uses a novel and proprietary method to isolate genomic DNA from variety of environmental samples. This kit has been successfully used to isolate DNA from tough-to-lyse bacteria, fungi, and algae that inhabit a range of samples including tap water, lake water, river water, and sewage samples. Isolated DNA can be used for most downstream applications including PCR, Southern blot, and SNP analysis.
DNase I , RNase-free Reference: EN401-02 DNase I (deoxyribonuclease I), that is, Deoxyribonuclease I, is an endodeoxyribonuclease that can digest single-stranded or double-stranded DNA. It recognizes and cleaves phosphodiester bonds to produce a 5'-end phosphate group Group, 3'-end hydroxyl monodeoxynucleotide or single-stranded or double-stranded oligodeoxynucleotide. The activity of DNase I depends on Ca2+ and can be activated by divalent metal ions Mg2+, Mn2+, etc. It exists in Mg2+ In the case of Mn2+, the enzyme can randomly recognize and cut any site on any strand of double-stranded DNA; and in the presence of Mn2+, it can recognize and cut almost the same site on both strands of DNA, resulting in blunt ends or There are sticky-end DNA fragments with 1-2 nucleotides protruding. This product has undergone strict quality control and is suitable for RNA extraction, in vitro transcription, DNA removal in RT-PCR experiments, DNase I footprinting, nick translatioin, DNA random fragment library construction and other molecular biology experiment. Application: High activity Very low RNase residue Good stability
E.Z.N.A.® Water DNA Kit Reference: D5525-01 The E.Z.N.A.® Water DNA Kit is formulated to isolate high-purity cellular DNA from water samples typically containing humic acid and inhibitors of PCR. This kit uses a novel and proprietary method to isolate genomic DNA from variety of environmental samples. This kit has been successfully used to isolate DNA from tough-to-lyse bacteria, fungi, and algae that inhabit a range of samples including tap water, lake water, river water, and sewage samples. Isolated DNA can be used for most downstream applications including PCR, Southern blot, and SNP analysis.
DNase I , RNase-free Reference: EN402-01 DNase I (deoxyribonuclease I), that is, Deoxyribonuclease I, is an endodeoxyribonuclease that can digest single-stranded or double-stranded DNA. It recognizes and cleaves phosphodiester bonds to produce a 5'-end phosphate group Group, 3'-end hydroxyl monodeoxynucleotide or single-stranded or double-stranded oligodeoxynucleotide. The activity of DNase I depends on Ca2+ and can be activated by divalent metal ions Mg2+, Mn2+, etc. It exists in Mg2+ In the case of Mn2+, the enzyme can randomly recognize and cut any site on any strand of double-stranded DNA; and in the presence of Mn2+, it can recognize and cut almost the same site on both strands of DNA, resulting in blunt ends or There are sticky-end DNA fragments with 1-2 nucleotides protruding. This product has undergone strict quality control and is suitable for RNA extraction, in vitro transcription, DNA removal in RT-PCR experiments, DNase I footprinting, nick translatioin, DNA random fragment library construction and other molecular biology experiment. Application: High activity Very low RNase residue Good stability
E.Z.N.A.® Soil DNA Kit Reference: D5625-00 The E.Z.N.A.® Soil DNA Kit is formulated to isolate high purity cellular DNA from soil samples typically containing humic acid and other inhibitors of PCR. This kit uses a novel and proprietary method to isolate genomic DNA from a variety of environmental samples without organic extractions. This kit has been successfully used to isolate DNA from Gram-positive and -negative bacteria, fungi, yeast, and algae that inhabit a range of samples including clay, sandy, peaty, chalky, or loamy soil samples. Isolated DNA can be used for most downstream applications, including PCR, Southern blot, and NGS analysis.
DNase I , RNase-free Reference: EN402-02 DNase I (deoxyribonuclease I), that is, Deoxyribonuclease I, is an endodeoxyribonuclease that can digest single-stranded or double-stranded DNA. It recognizes and cleaves phosphodiester bonds to produce a 5'-end phosphate group Group, 3'-end hydroxyl monodeoxynucleotide or single-stranded or double-stranded oligodeoxynucleotide. The activity of DNase I depends on Ca2+ and can be activated by divalent metal ions Mg2+, Mn2+, etc. It exists in Mg2+ In the case of Mn2+, the enzyme can randomly recognize and cut any site on any strand of double-stranded DNA; and in the presence of Mn2+, it can recognize and cut almost the same site on both strands of DNA, resulting in blunt ends or There are sticky-end DNA fragments with 1-2 nucleotides protruding. This product has undergone strict quality control and is suitable for RNA extraction, in vitro transcription, DNA removal in RT-PCR experiments, DNase I footprinting, nick translatioin, DNA random fragment library construction and other molecular biology experiment. Application: High activity Very low RNase residue Good stability
E.Z.N.A.® Soil DNA Kit Reference: D5625-01 The E.Z.N.A.® Soil DNA Kit is formulated to isolate high purity cellular DNA from soil samples typically containing humic acid and other inhibitors of PCR. This kit uses a novel and proprietary method to isolate genomic DNA from a variety of environmental samples without organic extractions. This kit has been successfully used to isolate DNA from Gram-positive and -negative bacteria, fungi, yeast, and algae that inhabit a range of samples including clay, sandy, peaty, chalky, or loamy soil samples. Isolated DNA can be used for most downstream applications, including PCR, Southern blot, and NGS analysis.
Bacteria RNA Plus Reagent Reference: R402-01 Bacteria RNA Plus Reagent is an auxiliary reagent optimized for RNA extraction from prokaryotes (including Gram-negative and Gram-positive bacteria). It can be used with Vazyme RNA Isolater Total RNA Extraction Reagent (R401-01) to greatly improve the RNA extraction of prokaryotes. Yield, while ensuring good product quality. Bacteria RNA Plus Reagent contains an optimized buffer system, chelating agents and mild protein denaturants. When extracting bacterial RNA, a high-temperature pretreatment is added before routine operations. Together with Vazyme RNA Isolater Total RNA Extraction Reagent, it can effectively inhibit endogenous RNase promotes protein denaturation, thereby increasing the yield and quality of bacterial RNA. This reagent is also suitable for extracting RNA from yeast and other fungi.Application: Greatly increase the amount of total RNA extracted from bacteria (gram-negative bacteria and gram-positive bacteria). To ensure good quality of RNA products, it is easier to meet the needs of subsequent experiments. The operation is simple, time-saving, no need for lysozyme or ultrasound and other breaking treatments, eliminating the RNA degradation that may be introduced by the operation. No bacterial genomic DNA contamination.
E.Z.N.A.® Soil DNA Kit Reference: D5625-02 The E.Z.N.A.® Soil DNA Kit is formulated to isolate high purity cellular DNA from soil samples typically containing humic acid and other inhibitors of PCR. This kit uses a novel and proprietary method to isolate genomic DNA from a variety of environmental samples without organic extractions. This kit has been successfully used to isolate DNA from Gram-positive and -negative bacteria, fungi, yeast, and algae that inhabit a range of samples including clay, sandy, peaty, chalky, or loamy soil samples. Isolated DNA can be used for most downstream applications, including PCR, Southern blot, and NGS analysis.