Biochemical Buffers and Reagents

Diamond Dye....a brilliant cut!

Diamond™ Nucleic Acid Dye provides a robust method for staining many gel types, along with the convenience of room temperature stability. It's more sensitive than ethidium bromide, so you use less sample and ladders for visualisation, saving you money with every gel you run.

Comparable in performance to SYBR^® Gold, it is compatible with denaturing and native agarose and polyacrylamide gels and can be imaged with any standard imaging system.

Diamond™ Nucleic Acid Dye does not require prewashing or destaining of gels.

Try Diamond Dye now for half price, that's just £27.50 for 500μl !

It's an automatic discount so to get Diamond Dye at half price please just order H1181!

Offer ends October 31st 2013.

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• See the comparison of the Diamond™ Nucleic Acid Dye, SYBR® Gold Nucleic Acid Gel Stain and SYBR® Safe DNA Gel Stain for detecting both DNA and RNA in agarose gels.

Acrylamide, Molecular Grade

Resolve very small DNA fragments, such as those generated by sequencing reactions, using polyacrylamide gel electrophoresis.

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Nuclease-Free Water

Our high-quality Nuclease-Free Water is tested and certified to be free of DNase and RNase activity.

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IPTG, Dioxane-Free

IPTG induces β-galactosidase activity by binding to and inhibiting the lac repressor, allowing you to differentiate recombinants from non-recombinants in cloning strategies using vectors containing the lacZ or lacZ α-peptide gene.

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X-Gal

X-Gal: Used in conjunction with IPTG to detect β-galactosidase activity. Tested for use with the pGEM®-Z vectors in chromogenicity assays.

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This Protocols and Applications Guide chapter provides basic information on preparing buffers for biochemical reactions.