DNA Extraction and Purification
Qiagen, Inc. DNEASY PLANT MINI KIT (250)
Kit, Plant Mini; DNeasy; For isolation of total cellular DNA from plant cells and tissues, or fungi; DNeasy Plant Mini Kit (250) Contents: 250 DNeasy Mini Spin Columns, 250 QIAshredder Spin Columns. Mini Kits also include: RNase
New England Biolabs, Inc. NEBNext Ultra II DNA PCR-free Library Prep Kit for Illumina - 96 rxn
The NEBNext Ultra II DNA PCR-free Library Prep Kit contains the enzymes and buffers required to convert a broad range of pre-fragmented DNA input amounts into libraries for next-generation sequencing on the Illumina platform all without an amplification step. The fast user-friendly workflow requires minimal hands-on time and maintains excellent library yields and GC coverage without requiring PCR. Dont be biased The NEBNext Ultra II DNA PCR-free Library Prep Kit for Illumina can save you time and minimize amplification-induced sequence bias and errors with a complete solution for PCR-free NGS library preparation. Built on the robust and reliable Ultra II reagents and workflow from New England Biolabs you can trust that your samples are in the best hands your own.
Qiagen, Inc. ENDOFREE PLASMID MEGA KIT (5)
EndoFree Plasmid Mega Kit (5), Contains: 5 QIAGEN-tip 2500, 5 QIAfilter Mega-Giga Cartridges, reagents, certified endotoxin-free buffers, and a comprehensive handbook. For purification of low-copy plasmids and cosmids
Abcam DNA Concentrator Kit, 50 Tests
The DNA Concentrator Kit (ab156895) is a complete set of essential components which enables the experimenter to efficiently concentrate DNA from various DNA samples with low concentration of DNA including those from microdissection samples and paraffin-embedded tissues.
The product is subject to the following: Abcam Restricted Use Statement
Macherey-Nagel Buffer A1 (1000 mL)
Buffer A1 (1000 mL) Resuspension Buffer A1, without RNase A bottle of 1000 mL
Zymo Research Corporation Quick-DNA/RNA FFPE Kit (50 Preps)
The unique chemistries of the product have been optimized for maximum recovery of DNA and of both large and small RNA species. Simply deparaffinize tissues using Deparaffinization Solution, digest using Proteinase K, heat to reverse chemical crosslinks, and then purify using Zymo-Spin™ Column technology. The result is high-quality DNA & total RNA (including small RNAs) that is DNA-free and is ready for RT/qPCR, hybridization, sequencing, etc.
VWR INTERNATIONAL Extracta DNA prep for PCR, 25 mL
Quanta's Extracta sample preparation system is a system that can be scaled to process various amounts of solid tissue in a simple and fast single-tube procedure. DNA may be purified from many tissue types and is suitable for use in sensitive downstream applications such as PCR, qPCR and High Resolution Melt Analysis.
Biotium Caldesmon, HMW (h-Caldesmon)(h-CALD), CF740 conjugate, 0.1mg/mL
Caldesmon HMW is the high molecular weight variant of Caldesmon. Two closely related variants of human caldesmon have been identified which are different in their electrophoretic mobility and cellular distribution. The h-caldesmon variant (120-150 kDa) is predominantly expressed in smooth muscle whereas l-caldesmon (70-80 kDa) is found in non- muscle tissue and cells. Neither of the two variants has been detected in skeletal muscle. This MAb recognizes only the 150 kDa variant (h-caldesmon) in Western blots of human aortic media extracts and is unreactive with fibroblast extracts from cultivated human foreskin. Caldesmon is a developmentally regulated protein involved in smooth muscle and non-muscle contraction.Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low
Biochain Institute Inc Genomic DNA - Congenital heart disease: Heart, 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.
Norgen Biotek Corp Genomic DNA Isolation Kit, 100 Prep
This kit is designed for the rapid preparation of genomic DNA from various tissue samples, cultured cells, viruses, bodily fluids and swabs using a rapid spin column protocol. Purified DNA is of an excellent yield and quality, and is immediately ready for any downstream application including PCR, qPCR, genotyping, sequencing and more. The protocol can be completed in approximately 80 minutes (including incubation time).
Macherey-Nagel NucleoSpin Blood XL, 50 preps
NucleoSpin Blood XL (50) 50 preps for the isolation of genomic DNA from blood - NucleoSpin Blood XL Columns, Collection Tubes, buffers, Proteinase K
Magbio Genomics Inc HighPrep PCR (250mL)
HighPrep™ PCR reagent is a post PCR and Next Gen library prep clean up system based on paramagnetic beads technology, designed for an efficient purification of PCR amplicons. The purification consists of removal of salts, primers, primer-dimers, dNTPs, as DNA fragments are selectively bound to the magnetic beads particles; and highly purified DNA is eluted with low salt elution buffer or water and can be used directly for downstream applications. The protocol can be adapted to your current liquid handling workstation (e.g. Beckman, Hamilton, Tecan, Caliper, Perkin Elmer, Agilent and Eppendorf) utilizing your current protocol as well as it can be performed manually.
Biochain Institute Inc Genomic DNA - Rat Normal Tissue: Lung, 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.
