Buffers

Lab Bioreagents Buffers have been developed through the screening of &gt2000 compounds with the support of machine learning (AI) and optimized through kinetic and dynamic binding tests. StrongBlock (I, II, III) are newly developed blocking buffers

Solution contains: Tris (hydroxymethyl) aminomethane: 2 M Acetic Acid: 1 M EDTA, Disodium Salt Dihydrate: 50 mM

TAE buffer premix powder: Each pack makes 1 L 1x25 TAE buffer or 25 liters of 1X TAE buffer. A single strength solution contains: 0.04 M Tris base 0.04 M Acetic acid 0.001 M EDTA

Tris-acetate provides electrical conductivity and maintains pH. EDTA inhibits metal dependent nucleases by chelating the divalent cations (Ca2 , Mg2 ), thus protecting the DNA from nucleases during the run.

NuSep&rsquos SingleShot Buffer pouches are perfect for standardizing your electrophoresis and Western blotting applications. Dissolve a pouch of pre-measured molecular biology-grade chemicals in 500mL of deionized water to obtain a ready-to-use 1x

TAE buffer 25x solution: TAE (Tris/Acetate/EDTA) Buffer is commonly used in nucleic acid electrophoresis. This solution has a lower buffering capacity than TBE buffer, but dsDNA runs faster with TAE buffer.

Tris-acetate provides electrical conductivity and maintains pH. EDTA inhibits metal dependent nucleases by chelating the divalent cations (Ca2 , Mg2 ), thus protecting the DNA from nucleases during the run.

Tris-acetate provides electrical conductivity and maintains pH. EDTA inhibits metal dependent nucleases by chelating the divalent cations (Ca2 , Mg2 ), thus protecting the DNA from nucleases during the run.

Tris-acetate provides electrical conductivity and maintains pH. EDTA inhibits metal dependent nucleases by chelating the divalent cations (Ca2 , Mg2 ), thus protecting the DNA from nucleases during the run.

Tris-acetate provides electrical conductivity and maintains pH. EDTA inhibits metal dependent nucleases by chelating the divalent cations (Ca2 , Mg2 ), thus protecting the DNA from nucleases during the run.

TAE buffer 25x solution: TAE (Tris/Acetate/EDTA) Buffer is commonly used in nucleic acid electrophoresis. This solution has a lower buffering capacity than TBE buffer, but dsDNA runs faster with TAE buffer.

10X solution contains: TRIS-Base: 0.4 M Acetic Acid: 0.2 M EDTA: 10 mM pH (10X Solution (@25&degC): 8.2-8.4