General Info
Omni Soft Tissue Tip™ Homogenizing Kit 10 x 115 mm Stainless Steel Generator Probe
- Ideal for PCR, RNA, and DNA sample preparation along with environmental, pharmaceutical, microbiological research and soft tissue analysis
- Omni Tips™ are economical and can be disposed of after use or autoclaved up to 7 times
- No need to order multiple items, everything is contained in one package
- Omni TH Motor has a variable speed controller that allows for speeds of 5,000 to 35,000 rpm
- Available with 5mm, 7mm, or 10mm stainless steel generator probes for more fibrous/tough samples
Ordering Information: Includes an Omni TH Motor, Omni Tip™ Adapter, 10 x 115 mm Stainless Steel Generator Probe, 12 Soft Tissue Omni Tips™, convenient storage box and instruction manual.
Specifications
- Processing Range (With Omni Tips): 0.25 mL-30 mL
- Power Rating: 125 watt
- Speed Control: Variable from 5,000-35,000 rpm
- Dimensions: 16 cm(6.5in) height, 5.1cm(2in) diameter.
- Weight: 538 g (19oz)
- Sound Level: < 72 db.
- Warranty: One year motor warranty
- Standards Approval: CSA and CE approved
Accessories
Videos
Applications
Product Downloads
In this study, we evaluate the potential for automated bead mill disruption of tissues for isolation of nuclei
from rat tissues and compare nuclei purity, nuclear proteome coverage and protein extraction reproducibility
to the extracts isolated by dounce and rotor stator homogenization. Following each extraction, nuclei were
isolated by centrifugation. Purity was then assessed by both microscopy and western blotting for known
nuclear and cytoplasmic protein markers. Proteins from each extraction method were then analyzed by LC-MS/
MS and protein extraction yields were quantified by spectral counting.
Literature
Product Downloads
In this study, we evaluate the potential for automated bead mill disruption of tissues for isolation of nuclei
from rat tissues and compare nuclei purity, nuclear proteome coverage and protein extraction reproducibility
to the extracts isolated by dounce and rotor stator homogenization. Following each extraction, nuclei were
isolated by centrifugation. Purity was then assessed by both microscopy and western blotting for known
nuclear and cytoplasmic protein markers. Proteins from each extraction method were then analyzed by LC-MS/
MS and protein extraction yields were quantified by spectral counting.