Category: Cell Culture

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Reference: LS01134

Prepared by a method developed at Worthington in which denatured, single-stranded calf thymus DNA is covalently bound to cellulose. Suitable for the purification of many proteins that are associated with nucleic acids such as DNA/RNA polymerases, endo- and exonucleases and reverse transcriptases. Supplied as a dry powder. One gram of DNA-cellulose will swell to 3 - 4ml when fully hydrated.

Reference: LS01200

Purified to an A260/A280 ≥1.8 from purified phage. Homogeneous by agarose gel electrophoresis. Generates the characteristic five and eight bands after digestion with EcoR I and Hind III respectively. A solution in 10 mM Tris-HCl, pH 8.0, with 1 mM EDTA.

Reference: LS01203

Purified to an A260/A280 ≥1.8 from purified phage. Homogeneous by agarose gel electrophoresis. Generates the characteristic five and eight bands after digestion with EcoR I and Hind III respectively. A solution in 10 mM Tris-HCl, pH 8.0, with 1 mM EDTA.

Reference: LS01206

Purified to an A260/A280 ≥1.8 from purified phage. Homogeneous by agarose gel electrophoresis. Generates the characteristic five and eight bands after digestion with EcoR I and Hind III respectively. A solution in 10 mM Tris-HCl, pH 8.0, with 1 mM EDTA.

Reference: LS01290

DNA fragments prepared by the digestion of purified lambda DNA with the restriction endonuclease EcoR I. On agarose gel electrophoresis the mixture separates into six individual bands having the following number of base pairs: 21226, 7421, 5804, 4878, 5643 and 3530. A solution in 10 mM Tris-HCl, pH 8.0, with 1 mM EDTA.

Reference: LS01293

DNA fragments prepared by the digestion of purified lambda DNA with the restriction endonuclease EcoR I. On agarose gel electrophoresis the mixture separates into six individual bands having the following number of base pairs: 21226, 7421, 5804, 4878, 5643 and 3530. A solution in 10 mM Tris-HCl, pH 8.0, with 1 mM EDTA.

Reference: LS01296

DNA fragments prepared by the digestion of purified lambda DNA with the restriction endonuclease EcoR I. On agarose gel electrophoresis the mixture separates into six individual bands having the following number of base pairs: 21226, 7421, 5804, 4878, 5643 and 3530. A solution in 10 mM Tris-HCl, pH 8.0, with 1 mM EDTA.

Reference: LS01300

DNA fragments prepared by the digestion of purified lambda DNA with the restriction endonuclease Hind III. On agarose gel electrophoresis the mixture separates into eight individual bands having the following number of base pairs: 23130, 9416, 6557, 4361, 2322, 2027, 564, and 125. (Note: A higher sample load may be required to clearly see the 564 and 125 base pair bands.) A solution in 10 mM Tris-HCl, pH 8.0, with 1 mM EDTA.

Reference: LS01303

DNA fragments prepared by the digestion of purified lambda DNA with the restriction endonuclease Hind III. On agarose gel electrophoresis the mixture separates into eight individual bands having the following number of base pairs: 23130, 9416, 6557, 4361, 2322, 2027, 564, and 125. (Note: A higher sample load may be required to clearly see the 564 and 125 base pair bands.) A solution in 10 mM Tris-HCl, pH 8.0, with 1 mM EDTA.

Reference: LS01306

DNA fragments prepared by the digestion of purified lambda DNA with the restriction endonuclease Hind III. On agarose gel electrophoresis the mixture separates into eight individual bands having the following number of base pairs: 23130, 9416, 6557, 4361, 2322, 2027, 564, and 125. (Note: A higher sample load may be required to clearly see the 564 and 125 base pair bands.) A solution in 10 mM Tris-HCl, pH 8.0, with 1 mM EDTA.

Reference: LS01430

DNA fragments prepared by the digestion of lambda DNA with the restriction endonuclease BstE II. On agarose gel electrophoresis the mixture separates into 14 individual bands having the following number of base pairs: 8454, 7242, 6369, 5686, 4822, 4324, 3675, 2323, 1929, 1371, 1264, 702, 224 and 117. A solution in 10 mM Tris-HCl, pH 8.0, with 1 mM EDTA.

Reference: LS01432

DNA fragments prepared by the digestion of lambda DNA with the restriction endonuclease BstE II. On agarose gel electrophoresis the mixture separates into 14 individual bands having the following number of base pairs: 8454, 7242, 6369, 5686, 4822, 4324, 3675, 2323, 1929, 1371, 1264, 702, 224 and 117. A solution in 10 mM Tris-HCl, pH 8.0, with 1 mM EDTA.