Designed for use with the Bioneer AccuPrep® 96-well plate series - handles 96 samples simultaneously for high throughput DNA extraction. Simply attach to a vacuum pump for easy processing of all AccuPrep 96-well plate DNA extraction kits.
The Tissue RNA PreMate™ kit is designed for total RNA extraction from tissue, cultured cells, leukocytes or serum. The PreMate protocol is based on a Modified guanidinium salt-lysis method to optimally extract total RNA. Extracted total RNA is treated with PreMate’s RNase-free DNase to eliminate any genomic DNA. The RNA Isolated with the Tissue RNA PreMate kit is suitable for Northern analysis, dot blot hybridization, poly A s…
Viral RNA PreMate contains all of the required reagents for easy isolation of total RNA from RNA viruses such as HCV using the guanidinium salt-lysis method. Possible sources include tissue, cultured cells, leukocytes, and serum. The extracted RNA can be used for molecular cloning, RT-PCR, Northern analysis, dot blot hybridization, poly-A (+) selection, RNase protection assays, and other application that require pure RNA. Vira…
DNA PrepMate™ - M is used to extract genomic DNA for PCR from microorganisms with tough cell walls (such as Mycobacterium tuberculosis complex and Mycoplasma pneumoniae) using a standard microwave oven. DNA preparation is accomplished quickly and efficiently. Source materials can be sputum, CSF, urine, pleural fluid or tissue.
DNA PrepMate™ II uses an optimal binding buffer and silica matrix to effectively isolate DNA from bacterial cells, PCR products, gel fragments and enzymatic reaction mixtures. Examples include the purification of DNA fragments or plasmid DNA from low-melting, TAE and TBE agarose gel, high salt solutions, and lysed bacterial cells (using alkaline lysis). DNA preparation is accomplished quickly and efficiently. The size range fo…
Phosphoramidites for DNA oligonucleotide synthesis, gene synthesis, and more. Features of DNA Phosphoramidites: Amine functions are protected by either a benzoyl or isobutyryl group {dA(Bz), dC(Bz), dG(Ib)}. The recommended procedure for cleavage and deprotection for standard oligonucleotide synthesis is incubation in a concentrated ammonia solution for 8 hours at 55 °C. The purities of manufactured nucleoside phosphora…
Phosphoramidites for RNA oligonucleotides synthesis and more.Features of RNA Phosphoramidites: Amine groups are protected by “either a benzoyl or isobutyryl group {dA(Bz), dC(Bz), dG(Ib)}. Cleavage and deprotection procedures for RNA synthesis is similar to DNA synthesis, with just an additional step to remove the 2'-OH protecting group. The 2'-OH group is protected by a tert-butyldimethylsilyl (TBDMS) group to prevent de…
Amino linker phosphoramidites for the functionalization of the 5'-end during oligo synthesisFeatures• Amino linker products are coupled with standard synthesis protocols, identical to the coupling of DNA monomer phosphoramidites.• 5'-Amino phosphoramidite is used to add a functional amine group at the 5'- or 3'- end of the oligonucleotides. The primary amino group can be used for subsequent conjugation of a variety of repo…
Spacer phosphoramidites for oligonucleotide synthesis. Wide range of lengthsA wide selection of linker lengths available: C3, C4, C6 and C12Features• The spacer phosphoramidite are used to put spacer arms into oligonucleotides.C3, C6 and C12 spacer phosphoramidite contain an aliphatic linker which can be added to oligo requiring longer spacer arms. In general terms, spacer phosphoramidites are used during oligonucleotide s…
Phosphoramidites for nucleic acid labeling, microarray labeling, and moreFeatures• Oligonucleotides modified with fluorescein derivatives can be used for genomic research, molecular diagnostics and molecular biology.• t-butylamine/H2O/MeOH is recommended for cleavage and deprotection steps of TAMRA modified oligos.• dI-phosphoramidite can perform as an universal base as it hybridizes with any of the four bases.Technical Info…
