Bio Basic

BS5852 96-Well Plate Bacterial Total RNA MiniPreps Super Kit

BS3692 BioBasic 96-Well Plate DNA Cleanup Mini-Preps Kit

BS3652 96-Well Plate PCR Products Purification Kit

96-Well Plate Plant Genomic DNA Mini-Preps Kit, BS8361, BioBasic

BS4152 EZ-10 96-Well Plate Plasmid DNA Mini-Preps The EZ-10 96 Well Spin Column Plasmid DNA Purification kit provides a simple, efficient and automated high throughput method for plasmid DNA purifications. Plasmid DNA is selectively adsorbed in silica gel-based. EZ-10 columns in the 96 Well Binding Plate and other impurities such as proteins, salts and nucleotides are removed. Plasmid DNA can be eluted in a small volume of Tris buffer.

96-Well Plate RNA Cleanup Concentration, BRC1251, BioBasic

96-Well Plate Yeast Genomic DNA Mini-Preps Kit, BS8357, BioBasic

PT92036

BS4372 EZ-500 Spin Column Endotoxin-Free Plasmid DNA Maxi-Preps Kit This kit is designed for fast isolation of genomic DNA from animal tissues. The kit contains a membrane embedded EZ-10 96 Well Binding Plate for binding genomic DNA in each well. Nucleotides, proteins, salts, and other impurities are washed away. Purified genomic DNA can be applied in most molecular biology experiments including restriction enzyme digestion, PCR, Southernblotting and so on. Applications: Genomic DNA purifica

SK1292 EZ-10 96-Well Plate Bacteria Genomic DNA Mini-Preps Kit: The kit provides a simple and convenient high throughout approach to isolate high quality Genomic DNa from both Gram negative and Gram positive bacteria. DNA of cell lysate is selectively adsorbed on EZ-10 Spin Column, impurities such as proteins, salts and nucleotides are washed away. No phenol/chloroform extraction or ethanol precipitation is required. Purified genomic DNA can be up to 50 kb in length and can be used for PCR, and

BT92031 EZ-10 96-Well Plate Blood Genomic DNA Mini-Preps Kit: 96-well Plate blood genomic DNA minipreps kit is designed for rapid and high-throughout purification of genomic DNA from fresh or frozen anticoagulated blood. Smaples are first lysed using proteinase K in an optimized buffer. The lysate using proteinase K in an optimized buffer. The lysate is then loaded onto the 96-well EZ plate, DNA is selectively bound to the EZ membrane embed in the plate in the presence of high concentrations of

VT92032 EZ-10 96-Well Plate Viral DNA Mini-Preps Kit: The kit provides a fast, simple and highly reproducible method for isolation of viral DNA from broad range cell-free clinical samples including serum, urine and plasma for clinical research and life science applications. Viral DNA in lysates is selectively absorbed in spin column and other impurities don't bind in the column. The procedure is simple and fast, no phenol extraction is required. Purified viral DNA can be used for PCR, Real Time

BS367 EZ-10 Spin Column DNA Cleanup Miniprep Kit: This DNA Cleanup kit provides a simple, efficient method for purification of DNA fragments from variable enzymatic reactions such as cDNA synthesis, ligation, restriction enzyme digestions, tailing, PCR*, alkaline phosphatase, nick translation, due terminators products from PCR** reaction mixture. It is also an ideal tool to desalt solution of DNA as well as to remove residual organic solvents or unincorporated nucleotides or primers (<40-mer) f

BS82312 EZ-10 Spin Column Animal Total RNA Mini-Preps Kit EZ‐10 Column Animal total RNA Purificaon Kit provides a simple spin column technique for preparaon of high quality, high‐purity intact total RNA. The reagent contains disrupve and protecve properes of guanidine isothiocyanate and β‐mercaptoethanol to inacvate the ribonucleases present in cell extracts. RNA in the whole homogeneity is selecvely absorbed on spin column and other impuries are washed away. Total RNA is eluted from the

EZ-10 Spin Column Blood Genomic DNA Mini-Preps Kit, SK8253, BioShop

EZ-10 Spin Column Blood RNA Miniprep Kit BS82313 EZ-10 Column Blood RNA Purification Kit provides a simple spin column technique for preparation of high quality, high-purity intact total RNA. The reagent contains disruptive and protective properties of guanidine isothiocyanate and ß-mercaptoethanol to inactivate the ribonucleases present in cell extracts. RNA in the whole homogeneity is selectively absorbed on spin column and other impurities are washed away. Total RNA is eluted from the membr