The FastDNA® SPIN Kit for Feces Designed for use with the FastPrep® Instruments, host cells as well as bacteria, fungi, viruses, protists and other cells present in fecal samples are easily lysed within 40 seconds. These benchtop devices use a unique, optimized motion that provide an ext...
快速高效提取粪便DNA,可裂解任何粪便样品。可直接用于PCR等其下游实验,配合FastPrep仪器使用无需研磨样品。 The FastDNA® SPIN Kit for Feces Designed for use with the FastPrep® Instruments, host cells as well as bacteria, fungi, viruses, protists and other cells present in fecal samples are easily...
A common CTAB buffer recipe is: 2% CTAB, 1% polyvinyl pyrrolidone, 100 mM Tris-HCl, 1.4 M NacL, 20 mM EDTA. Alkaline extraction: Routinely used to isolate plasmid DNA from bacteria samples. Exposing harvested bacteria to highly alkaline solutions and sodium dodecyl sulfate removes proteins and ...
The released DNA is purified by a silica-based spin filter method and is suitable for PCR analysis and other downstream applications. Complete lysis of all organisms, including historically difficult sources such as eubacterial spores and endospores, gram positive bacteria, yeast, algae, nematodes ...
FastDNA SPIN Kit for Soil(mpbio土壤DNA提取试剂盒产品说明书-北京毕特博生物)
The FastDNA® SPIN Kit is designed for use with any FastPrep® Instrument, plant and animal tissues, bacteria, algae, fungi spores and other members of a soil population are easily lysed within 40 seconds. These benchtop devices use a unique, optimized motion to homogenize samples by simultan...
The kit enables the extrac- tion of genomic DNA from all bacteria, fungi, plants and animals in a soil community. The kit consists of three general components: 1. Lysing Matrix The Lysing Matrix E tubes contain a mixture of ceramic and silica particles des- gined to efficiently lyse all ...
When recombinant p14 and MP1 were individually expressed in bacteria, solubility of these proteins was extremely poor, and only large aggregates were seen. Structurally, a p14-p14 dimer is unfavorable due to steric incompatibilities, especially between side chains of residues located on helix α2...
To prevent contamination by bacteria and mycoplasma, cells were pretreated with Nanomycopulitine reagent (L-X16-010; Biowest, Nuaillé, France). The viral particles were purified from the culture medium by ultracentrifugation. An empty virus was used as control. Viral titers were determined by ...
In the case of DiOC2(3), this accumulation is accompanied by a shift from green to red emission due to dye stacking, allowing the use of a ratiometric parameter (red/green fluorescence ratio) that corrects for size differences whe...