Agarose I has low electroendosmosis (EEO) and high electrophoresis mobility. Suitable for nucleic acid analytical and preparative electrophoresis; blotting; and protein electrophoresis (i.e. Radial Immunodiffusion).
Moisture: ≤ 7%
Agarose II has a low melting and gelling temperature compared to standard agaroses. The low melting temperature allows for the recovery of undamaged nucleic acids below the denaturation temperature. The low gelling temperature ensures that the agarose will be in a liquid state at a ..
Agarose IV is a linear polymer with a very high molecular weight, giving gel structures unlike those of traditional agaroses. This characteristic produces a strong intercatenary interaction, yeilding a gel with very high gel strength and higher exclusion limit.
For improved resolution..
Agarose MS is a high purity, ultra high resolution small fragment analysis agarose.
Moisture: ≤ 10%
Ash: ≤ 0.5%
EEO (electroendosmosis): ≤ 0.1
Sulfate: ≤ 0.1%
Gel Strength 1.5% (g/cm2): ≥ 750
Gelling Temperature 1.5% (ºC): ≤ 33
TAE Running Buffer is offered as a 50X concentrated solution or 20 x 1L dry buffer packs of Tris base, acetic acid and EDTA. The primary use of TAE Running Buffer is in agarose electrophoresis for the separation of nucleic acids (DNA and RNA). TAE has a lower buffer capacity than TBE Runn..
TBE Running Buffer is offered as a 10X concentrated solution or 20 x 1L dry buffer packs of Tris base, boric acid and EDTA. The primary use of TBE Running Buffer is in agarose electrophoresis for the separation of nucleic acids (DNA and RNA).
10X Concetrated Solution:&nb..
Loading buffer to resolve single-stranded DNA oligos or RNA into sharp, distinct bands. For the analysis and purification of products ranging from 20-800 bases, making them an ideal choice for synthetic oligo analysis and purification, RNase Protection Assays (RPA), in vitro transcription studies, a..