Life Science

An inhibitor of the initiation of translation that blocks the interaction of eIF4G with eIF4E (KD = 25 &muM) prevents the expression of oncogenic proteins in mammalian cancer cells, leading to apoptosis blocks translation in some viruses that do

4X LDS Sample Buffer is used to prepare protein samples for denaturing polyacrylamide gel electrophoresis (PAGE) with SurePAGE&trade, ExpressPlus&trade and most other types of Bis-Tris gels. LDS sample buffer contains lithium dodecyl sulfate with

4X LDS Sample Buffer is used to prepare protein samples for denaturing polyacrylamide gel electrophoresis (PAGE) with SurePAGE&trade, ExpressPlus&trade and most other types of Bis-Tris gels. LDS sample buffer contains lithium dodecyl sulfate with

The Mag-Bind&reg Blood & Tissue DNA HDQ 96 Kit is designed for isolation of high-quality genomic DNA from blood samples, saliva, swabs, mouse tails, dried blood spots or cultured cells. Mag-Bind&reg Particles HDQ provides quick magnetic response

The Mag-Bind&reg Environmental DNA 96 Kit allows rapid and reliable isolation of high-quality DNA from soil and water samples. The Mag-Bind&reg Environmental DNA 96 Kit can isolate microbial DNA from yeast, fungi, and gram-positive or negative

The Mag-Bind&reg Plant DNA DS 96 Kit allows rapid and reliable isolation of high-quality genomic DNA from plants and other tissues that are particularly difficult to lyse or very high in polysaccharide content. The lysis and binding buffers are

The Mag-Bind&reg family of products is an innovative system that radically simplifies extraction and purification of nucleic acids from a variety of sources. Key to the system is Omega Bio-tek&rsquos proprietary Mag-Bind&reg Particle that avidly,

Mag-Bind&reg Viral DNA/RNA Kit is designed for the rapid and reliable isolation of viral RNA and viral DNA from serum, swabs, plasma, saliva, and other body fluids. The Mag-Bind&reg magnetic beads technology enables purification of high-quality

The E.Z.

The E.Z.

The E.Z.

Gel purification of DNA is a common technique used for the isolation of specific DNA fragments from reaction products. However, most methods either fail to completely remove agarose, which can lead to problems in downstream manipulations shear the