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Chemical reagents, kits, columns, and other products used for DNA synthesis, and to subsequently run purification columns; includes genetic assembly systems.
The Enceed T cell Activation reagent induces T cell activation and expansion in enriched T cells or PBMCs The Enceed T cell Activation reagent is composed of biodegradable matrix-coated nanoparticles conjugated with mouse anti-human CD3 and mouse anti-human CD28 antibodies The small sized particulate structure of the activation reagent enables its easy removal by media washing or centrifugation
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Reporter Cells are prepared using INDIGO’s proprietary CryoMite™ process. This cryopreservation method yields high cell viability post-thaw and provides the convenience of immediately dispensing healthy reporter cells into assay plates. There is no need for intermediate preparatory steps such as the spin-and-rinse of cells, viability determinations, or cell titer adjustments prior to assay setup.
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DNA Polymerase I, Large (Klenow) Fragment is a proteolytic product of E. coli DNA Polymerase I which retains polymerization and 3' to 5' exonuclease activity, but has lost 5' to 3' exonuclease activity. Klenow retains the polymerization fidelity of the holoenzyme without degrading 5' termini.
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The LGC Biosearch Technologies MM1-3500-1 is a Universal Support Column optimized for 1 μmol oligonucleotide synthesis. Made with controlled-pore glass, this product features a 1000 Å pore size and utilizes a DMT-off design, ensuring a faster cleavage rate and simplifying the synthesis process. This universal support allows for the flexibility of determining the 3'-end nucleobase during the initial phosphoramidite addition, promoting easier supply chain management for oligonucleotide synthesis applications.
Product type: Universal support column
Solid support material: Controlled-pore glass (CPG)
Pore size: 1000 Å
Functional loading: Up to 55 μmol/g
DMT status: DMT off (unprotected)
Linker type: N-iPr (isopropyl)
Linker cleavage rate: 5 times faster than N-Ph version
Synthesis scale: 1 μmol
Column type: MerMade
Application: Oligonucleotide synthesis
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MW 1204.8 g/mol, Purity >98%. Activates Ca²+-insensitive PKC isotypes δ, ε and η in vitro. Binds to the general receptor for phosphoinositide-1 (GRP1) protein through a plekstrin homology (PH) domain.
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The NEBNext Single Cell/Low Input cDNA Synthesis and Amplification Module uses a template switching method to generate full length cDNAs directly from single cells or 2 pg - 200 ng RNA. This unique workflow enables generation of high quality sequencing data from a broad range of inputs, and superior transcript detection, while providing reliably consistent performance
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MW 285.39 g/mol, Purity >98%. First selective small conductance Ca²+-activated K+ channel (SK) activator. Selectively opens SK2 and SK3 channels (EC₅₀ values are 5.6 and 14 μM, respectively). Shows no activity at SK1 and IK. Additionally reduces activity and excitability of dopamine neurons. Active in vivo.