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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.
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.
The Novatia Oligo HTCS High Temp Trap Column is engineered for robust performance in HPLC applications, making it ideal for oligonucleotide high-throughput characterization systems. This column can withstand elevated temperatures and pressures up to 6,000 PSI, facilitating efficient online desalting and purification crucial for accurate oligonucleotide LC/HRMS analysis. Supplied as a convenient four-pack, it ensures continuity in high-demand scientific workflows.
Designed for HPLC applications
Maximum pressure rating of 6,000 PSI
Suitable for elevated temperature conditions
Pack includes 4 columns
Compatible with Oligo HTCS LC/MS systems
Requires Oligo HTCS High Temp Trap Holder
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The Ph.D.-7 Phage Display Peptide Library Kit v2 is based on a combinatorial library of random heptapeptides fused to the N-terminus of a minor coat protein (pIII) of M13 phage. The peptide is followed by a short spacer (Gly-Gly-Gly) which directly precedes the wild-type pIII sequence. The library consists of about 1E09 electroporated sequences amplified once to yield approximately 100 copies of each sequence in 10 ul of the supplied phage. The Ph.D.-7 Phage Display Peptide Library Kit v2 contains the Ph.D.-7 Phage Display Peptide Library a DYKDDDDK Mouse monoclonal antibody and Protein G Magnetic Beads for a panning control experiment and enough -96gIII sequencing primer for greater than 50 sequencing reactions.
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The Ph.D.-12 Phage Display Peptide Library Kit v2 is based on a combinatorial library of random dodecapeptides fused to the N-terminus of a minor coat protein (pIII) of M13 phage. The peptide is followed by a short spacer (Gly-Gly-Gly) which directly precedes the wild-type pIII sequence. The library consists of about 1E09 electroporated sequences amplified once to yield approximately 100 copies of each sequence in 10 ul of the supplied phage. The Ph.D.-12 Phage Display Peptide Library Kit v2 contains the Ph.D.-12 Phage Display Peptide Library a DYKDDDDK Mouse monoclonal antibody and Protein G Magnetic Beads for a panning control experiment and enough -96gIII sequencing primer for greater than 50 sequencing reactions.
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Microparticle Activation Buffer (1 L) is an optimized versatile buffer for the conjugation of antibodies proteins peptides and small molecules to polystyrene (Latex) microparticles and nanoparticles This buffer can be used to dilute particles from stock solutions activate particles for covalent linkage (such as NHS and EDC activation) and wash particles after activation and before conjugation For in vitro research use only
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