Genome Analysis Products & Reviews

DNA PrepMate™ II uses an optimal binding buffer and silica matrix to effectively isolate DNA from bacterial cells, PCR products, gel fragments and enzymatic reaction mixtures. Examples include the purification of DNA fragments or plasmid DNA from low-melting, TAE and TBE agarose gel, high salt solutions, and lysed bacterial cells (using alkaline lysis). DNA preparation is accomplished quickly and efficiently. The size range fo…

Top DNA polymerase is a novel thermostable DNA polymerase that is more processive than Taq DNA polymerase. In fact, the extension rate of Top DNA Polymerase is > 3 x that of Taq DNA Polymerase! Top DNA Polymerase can be used for a variety of PCR applications (including TA cloning) and is a robust enzyme for everyday PCR. It contains no proofreading or 5’-3’ Exonuclease activity.Features and Benefits• Fast: More than three tim…

Get more cDNA in less time with CycleScript Reverse Transcriptase. CycleScript is a versatile reverse transcriptase - applicable to both conventional Reverse Transcription and Cyclic Reverse Transcription (Cyclic RT, patent pending – for cDNA amplification). It features high activity across a wide range of temperatures from 37 to 55°C; therefore, reverse transcription is carried out like PCR. The Cyclic RT reaction is composed…

Moloney Murine Leukemia Virus (M-MLV) Reverse Transcriptase is an RNA-dependent DNA polymerase. This enzyme is able to use an RNA molecule as a template and synthesize a double-strand DNA. M-MLV Reverse Transcriptase is isolated from a E.coli strain containing a recombinant clone. It is ideal for use of first-strand synthesis cDNA from RNA molecules and for cDNA synthesis for Reverse Transcriptase PCR and qRT-PCR.

Bioneer is pleased to offer our Custom Gene synthesis service to help customers save time and money while improving research results. Gene synthesis is the most cost effective way to enhance your research. In as little as 2 weeks, you can have your Gene cloned in hand and 100% sequence guaranteed. And with Bioneer’s great pricing it can cost less to order a synthetic gene from us than to buy all the kits and reagents necessary…

Gene cloning and subcloning of genes into any cloning vector you want - 100% sequence guaranteed.

The fastest and most cost effective way to construct a mutant library for protein structure and function research or to increase enzyme function is to use our Point Mutation Service combined with our Gene Synthesis Service. Site-directed mutation such as Point Mutation as well as deletion mutation services are available. For unsurpassed quality and value pricing, partner with Bioneer today!

25/100 bp Mixed DNA Ladder is designed for determining the size of double stranded DNA from 25 to 2,000 bp. The ladder consists of 17 double stranded DNA fragments ranging in size from 25 to 200 bp in 25 bp increments, from 200 to 1,000 bp in 100 bp increments, and an additional fragment of 2,000 bp. The DNA marker fragments at 150, 500, 1,000 and 2,000 bp bands are two times brighter for easy identification.

25/100 bp Mixed DNA Ladder is designed for determining the size of double stranded DNA from 25 to 2,000 bp. The ladder consists of 17 double stranded DNA fragments ranging in size from 25 to 200 bp in 25 bp increments, from 200 to 1,000 bp in 100 bp increments, and an additional fragment of 2,000 bp. The DNA marker fragments at 150, 500, 1,000 and 2,000 bp bands are two times brighter for easy identification.

100 bp DNA Ladder was designed to determine the size of double stranded DNA fragments from 100 to 2,000 bp. The 100 bp DNA Ladder consists of 13 double stranded molecular weight markers ranging in sizes from 100 to 1,000 bp in 100 bp increments, and additional fragments of 1,200, 1,600, 2,000 bp. The 500, 1,000 and 2,000 bp bands are two times brighter for easy identification.

100 bp DNA Ladder was designed to determine the size of double stranded DNA fragments from 100 to 2,000 bp. The 100 bp DNA Ladder consists of 13 double stranded molecular weight markers ranging in sizes from 100 to 1,000 bp in 100 bp increments, and additional fragments of 1,200, 1,600, 2,000 bp. The 500, 1,000 and 2,000 bp bands are two times brighter for easy identification.

100 bp Plus DNA Ladder was designed to determine the size of double stranded DNA fragments from 100 to 10,200 bp. The 100 bp Plus DNA Ladder consists of 19 double stranded molecular weight markers, ranging in size from 100 to 1,000 bp in 100 bp increments, and additional fragments of 1,200, 1,600, 2,000, 2,961, 4,000, 5,007, 5,991, 8,000, 10,200 bp. The 200, 1,000 and 2,000 bp bands are two times brighter for easy identificati…

100 bp Plus DNA Ladder was designed to determine the size of double stranded DNA fragments from 100 to 10,200 bp. The 100 bp Plus DNA Ladder consists of 19 double stranded molecular weight markers, ranging in size from 100 to 1,000 bp in 100 bp increments, and additional fragments of 1,200, 1,600, 2,000, 2,961, 4,000, 5,007, 5,991, 8,000, 10,200 bp. The 200, 1,000 and 2,000 bp bands are two times brighter for easy identificati…

1 kb DNA Ladder is designed for determining the size of double stranded DNA ranging between 500 to 10,000 bp. The 1 kb Ladder consists of DNA fragments 0.5, 1.0, 1.6, 2.0, 3 (2.961), 4, 5 (5.007), 6 (5.991), 8 and 10 (10.2) kb. The 2.961 kb band is approximately two times brighter for easy identification.

1 kb DNA Ladder is designed for determining the size of double stranded DNA ranging between 500 to 10,000 bp. The 1 kb Ladder consists of DNA fragments 0.5, 1.0, 1.6, 2.0, 3 (2.961), 4, 5 (5.007), 6 (5.991), 8 and 10 (10.2) kb. The 2.961 kb band is approximately two times brighter for easy identification.

Lambda DNA/EcoR I Marker is created by digesting lambda DNA with the restriction enzyme EcoR I. The resulting DNA ladder is then purified and buffer and dye are added so the DNA marker is ready to load. Lambda DNA/EcoR I Marker consist of 6 double stranded lambda DNA fragments ranging in size from 3,530 to 21,226 bp.

Lambda DNA/EcoR I Marker is created by digesting lambda DNA with the restriction enzyme EcoR I. The resulting DNA ladder is then purified and buffer and dye are added so the DNA marker is ready to load. Lambda DNA/EcoR I Marker consist of 6 double stranded lambda DNA fragments ranging in size from 3,530 to 21,226 bp.

Lambda DNA/Hind III DNA Marker is generated by digesting lambda DNA with restriction enzyme Hind III. The resulting DNA Ladder is then purified, and buffer and dye are added so the marker is ready to load. Lambda DNA/Hind III Marker consist of 8 double stranded Lambda DNA fragments ranging in size from 125 to 21,226 bp, making it an ideal molecular weight marker for daily use.

Lambda DNA/Hind III DNA Marker is generated by digesting lambda DNA with restriction enzyme Hind III. The resulting DNA Ladder is then purified, and buffer and dye are added so the marker is ready to load. Lambda DNA/Hind III Marker consist of 8 double stranded Lambda DNA fragments ranging in size from 125 to 21,226 bp, making it an ideal molecular weight marker for daily use.

Lambda DNA/EcoR I + Hind III DNA Marker is generated by digesting lambda DNA with two restriction enzymes EcoR I and Hind III. The resulting DNA Ladder is then purified and buffer and dye are added so the marker is ready to load. Lambda DNA/EcoR I + Hind III Marker consist of 13 double stranded Lambda DNA fragments ranging in size from 125 to 21,226 bp, making it an ideal molecular weight marker for daily use.

Lambda DNA/EcoR I + Hind III DNA Marker is generated by digesting lambda DNA with two restriction enzymes EcoR I and Hind III. The resulting DNA Ladder is then purified and buffer and dye are added so the marker is ready to load. Lambda DNA/EcoR I + Hind III Marker consist of 13 double stranded Lambda DNA fragments ranging in size from 125 to 21,226 bp, making it an ideal molecular weight marker for daily use.

Assays for methylases, acetylases, phosphorylases and other modifying enzymes involved in histone and chromatin modulation are developed and optimized by RapidFire scientists for primary and secondary screens. Although histone modifying enzymes can be difficult to analyze by traditional methods, label-free RapidFire technology is well suited to this novel and emerging class of targets.

The Montage Plasmid Miniprep96 Kit is a fast, easy-to-use kit for high-purity plasmid minipreps. Using a unique separation technology (patent pending), the Montage Kit follows a simple protocol that eliminates lengthy bind/elute methods and centrifugation steps to yield clean and reproducible DNA in 50% less time than traditional methods.The kit includes all the reagents and disposable materials you need to purify plasmid DNA…