Molecular Biology

DNA polymerase I (holoenzyme) has 5&#8242&#85943&#8242 and 3&#8242&#85945&#8242 exonuclease activities in addition to its synthetic activity. This bifunctional activity enables the enzyme to use nicks or gaps in double stranded DNA as

DNA polymerase I yields two fragments (small and large) upon protease digestion. The large fragment (Klenow fragment) loses the 5&#8242 exonuclease activity that is present in the intact holoenzyme.

DNA polymerase I yields two fragments (small and large) upon protease digestion. The large fragment (Klenow fragment) loses the 5&#8242 exonuclease activity that is present in the intact holoenzyme.

Thermo Sequenase is a novel thermostable DNA polymerase that uses dideoxynucleotide triphosphates (ddNTPs) as readily as deoxynucleotide (dNTP) substrates. Uniform and easy-to-read band patterns.

Obtaining DNA from biological samples is the first and most crucial step in molecular biology. Eluting both high quality and high yield of DNA from a wide range of biological samples can be challenging and can impact the success of downstream

Obtaining DNA from biological samples is the first and most crucial step in molecular biology. Eluting both high quality and high yield of DNA from a wide range of biological samples can be challenging and can impact the success of downstream

The kit has all the reagents necessary for quantitation of DNA using the fluorescent dye bisBenzimide (Hoechst 33258). The kit allows highly sensitive, quick, and accurate determinations of double-stranded DNA from 10ng/ml to 5&#956g/ml, even in

Obtaining DNA from biological samples is the first and most crucial step in molecular biology. Eluting both high quality and high yield of DNA from a wide range of biological samples can be challenging and can impact the success of downstream

Aflatoxins are mycotoxins found in foods and livestock feeds that were initially produced by species of Aspergillus. Aflatoxin M1 is the hydroxylated metabolite of aflatoxin B1 it inhibits DNA synthesis and induces cell cycle arrest.

DNA-Erase&trade is a non-alkaline, non-corrosive and non-carcinogenic cleansing solution that is highly active against DNA contamination and is intended for use at PCR workstations for eliminating PCR artifacts from all laboratory surfaces,

A cell-permeable benzochromenone compound that acts as a potent, specific, reversible, and ATP-competitive inhibitor of DNA-PK with an IC 50 of 0.23 &#181M.

A morpholino-benzophenone compound that acts as a potent, selective, reversible, and ATP-competitive inhibitor of DNA-PK (IC 50 = 270 nM). Inhibits PI 3-K catalytic subunit p110-isozymes at higher concentrations (IC 50 = 32 &#181M, 3.