Category: Cell Culture

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  • Categories: Powder media
Reference: LS009070

A highly purified preparation supplied as a lyophilized powder.

Reference: LS009071

A highly purified preparation supplied as a lyophilized powder.

Reference: LS01120

Prepared by a method developed at Worthington in which native, double-stranded calf thymus DNA is covalently bound to cellulose. Suitable for the purification of many DNA binding proteins such as polymerases, transcription factors, and terminators, etc. Supplied as a dry powder. One gram of DNA-cellulose will swell to 3 - 4ml when fully hydrated.

Reference: LS01122

Prepared by a method developed at Worthington in which native, double-stranded calf thymus DNA is covalently bound to cellulose. Suitable for the purification of many DNA binding proteins such as polymerases, transcription factors, and terminators, etc. Supplied as a dry powder. One gram of DNA-cellulose will swell to 3 - 4ml when fully hydrated.

Reference: LS01124

Prepared by a method developed at Worthington in which native, double-stranded calf thymus DNA is covalently bound to cellulose. Suitable for the purification of many DNA binding proteins such as polymerases, transcription factors, and terminators, etc. Supplied as a dry powder. One gram of DNA-cellulose will swell to 3 - 4ml when fully hydrated.

Reference: LS01130

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: LS01132

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: 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.