DNA Extraction and Purification
Macherey-Nagel NucleoBond Xtra Maxi EF, 50 preps
NucleoBond Xtra Maxi EF (50) 50 preps for the isolation of endotoxin-free plasmid DNA - NucleoBond Xtra Maxi Columns, NucleoBond Xtra Maxi Column Filters, buffers, RNase A
Molecular Research Center DNAZOL 50ML
Genomic DNA isolation reagent for use with tissues, cells and liquids. The isolation is fast (10-30 min), simple and reliable. Non-toxic. 1 ml of DNAzol isolates DNA from 25-50 mg tissue or 1-3 x 107 cells.
Biochain Institute Inc Genomic DNA - Mouse Normal Tissue: Heart, 100 ug/PK
BioChain's tissue genomic DNAs are isolated from a wide variety of tissues using a proprietary modified guanidine thiocyanate technique. The quality and purity of genomic DNA are tested by spectrophotometer and electrophoresis. A260/280 is between 1.8 and 2.0, and A260/230 is >2.0 (detected in 10 mM Tris-Cl, pH 7.5). Contamination of RNA, polysaccharides and proteoglycans has been effectively eliminated.
Cayman Chemical Fungal Lysergol 25mg
An ergot alkaloid and 5-HT1A, 5-HT2A, and 5-HT2C receptor agonist (EC50s = 73, 1.6, and 6.6 nM, respectively, in a FLIPR assay); induces contractions in isolated rat tail arteries (EC50 = 436.5 nM); enhances the antibacterial activity of nalidixic acid against susceptible and drug-resistant E. coli at 10 UG/ml
Biochain Institute Inc Genomic DNA - Liver Cirrhosis: Rectum, from a single donor, 50 ug/PK
BioChain's tissue genomic DNAs are isolated from a wide variety of tissues using a proprietary modified guanidine thiocyanate technique. The quality and purity of genomic DNA are tested by spectrophotometer and electrophoresis. A260/280 is between 1.8 and 2.0, and A260/230 is >2.0 (detected in 10 mM Tris-Cl, pH 7.5). Contamination of RNA, polysaccharides and proteoglycans has been effectively eliminated.
Biochain Institute Inc Genomic DNA - Alzheimer's Disease: Brain: Precentral Gyrus, from a single donor, 50 ug/PK
BioChain's tissue genomic DNAs are isolated from a wide variety of tissues using a proprietary modified guanidine thiocyanate technique. The quality and purity of genomic DNA are tested by spectrophotometer and electrophoresis. A260/280 is between 1.8 and 2.0, and A260/230 is >2.0 (detected in 10 mM Tris-Cl, pH 7.5). Contamination of RNA, polysaccharides and proteoglycans has been effectively eliminated.
Boca Scientific Inc Buccalyse Rapid Buccal Cell DNA Isolation Kit, 50 Extractions, with 50 SK-1S Buccal Swabs
The BEK-50/SK1 kit includes 50 SK-1S Buccal Swabs and the Buccalyse DNA extraction kit for 50 samples. SK-1S Buccal Swabs are designed for high-yield DNA retrieval and convenient transport. Each SK-1S buccal swab is packaged with a 5ml plastic collection tube and cap. The Buccalyse DNA Extraction Kit, specifically designed for use with buccal swabs, includes one solution for a fast and simple one tube method for extracting DNA from buccal swabs. In only 20 minutes, this kit provides PCR-ready DNA that does not require centrifugation.
Bioworld Plasmid DNA Isolation Solution III, 250 mL
Plasmid DNA Isolation, Solution III Common buffer used for DNA isolation Technical Information: 5M Potassium Acetate (60ml) Glacial Acetic Acid (11.5ml) H2O (28.5ml) Resulting solution is 3M with respect to potassium and 5M with respect to acetate.
Zymo Research Corporation ZymoPURE™ P2 (Green) (3 ml)
ZymoPURE P2 (Blue) is designed to be used with our ZymoPURE Plasmid Purification Kits, which is the fastest and simplest method available to efficiently isolate transfection-grade plasmid DNA from E. coli
Biochain Institute Inc Control Genomic DNA - Cynomolgus Monkey Female, 100 ug/PK
BioChain's tissue genomic DNAs are isolated from a wide variety of tissues using a proprietary modified guanidine thiocyanate technique. The quality and purity of genomic DNA are tested by spectrophotometer and electrophoresis. A260/280 is between 1.8 and 2.0, and A260/230 is >2.0 (detected in 10 mM Tris-Cl, pH 7.5). Contamination of RNA, polysaccharides and proteoglycans has been effectively eliminated.
Bulldog Bio Inc FastGene Scriptase II ReadyMix (100 rxns), OdT & Random Hex-primers
How would you construct the ideal reverse transcriptase? It would have to make very long cDNAs at high yields. It would have to be able to work from very small amounts of input RNA. And of course, it would have to work fast. FastGene Scriptase II checks all three boxes, and it does it at a reasonable price. Here’s how. First, mutations are inserted into the RNase H domain of native MuLV‘s reverse transcriptase delivering a higher yield of full-length cDNAs. Next, changes are made to increase the enzymes natural thermal stability providing a more robust enzyme that doesn’t lose processing power, even at elevated temperatures. Finally, the reaction buffer composition is optimized for high speed production of cDNAs from incredibly low levels of input RNA. This unique combination of size, speed, and production makes FastGene Scriptase II the optimal choice for even the most complex applications requiring cDNAs, such as RT-qPCR and NGS.
10X Genomics Inc Library Construction Kit, 16 rxns
The Chromium Next GEM Single Cell Multiome ATAC + Gene Expression workflow produces sequencing-ready Multiome ATAC and Gene Expression libraries from the same single nuclei, enabling simultaneous epigenomic and gene expression profiling.
Bulldog Bio Inc FastGene Scriptase II ReadyMix (100 rxns), Random Hex-primers
How would you construct the ideal reverse transcriptase? It would have to make very long cDNAs at high yields. It would have to be able to work from very small amounts of input RNA. And of course, it would have to work fast. FastGene Scriptase II checks all three boxes, and it does it at a reasonable price. Here’s how. First, mutations are inserted into the RNase H domain of native MuLV‘s reverse transcriptase delivering a higher yield of full-length cDNAs. Next, changes are made to increase the enzymes natural thermal stability providing a more robust enzyme that doesn’t lose processing power, even at elevated temperatures. Finally, the reaction buffer composition is optimized for high speed production of cDNAs from incredibly low levels of input RNA. This unique combination of size, speed, and production makes FastGene Scriptase II the optimal choice for even the most complex applications requiring cDNAs, such as RT-qPCR and NGS.