DNA Synthesis Reagents and Columns
Abcam NS 1619, KCa1.1 channel activator, 5MG
MW 362.23 Da, Purity >98%. Potent and selective KCa1.1 channel activator. Induces a concentration-dependent decrease in mitochondrial membrane potential (EC50 = 3.6 μM).
The product is subject to the following: Abcam Restricted Use Statement
Sigma Aldrich Fine Chemicals Biosciences H-Asp(OtBu)-2-ClTrt resin | MFCD00801403 | 5 g
H-Asp(OtBu)-2-ClTrt resin | Mol Wt: 172.21 | MFCD00801403 | 5 g
Glen Research 0.02M IODINE IN TETRAHY2,000ML
0.02M Iodine in Tetrahydrofuran/Pyridine/Water (70:20:10) 2,000mL
Cayman Chemical Humn ActIvatr ProteIn1 Rep 96
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.
Genscript Corporation Enceed T cell Activation hum
The Enceed T cell Activation human (GMP) is used for in vitro activation and expansion of enriched T cells or peripheral blood mononuclear cells (PBMCs) Due to the nanoscale structure of Enceed T cell Activation human (GMP) the excess reagent can be removed by centrifugation or conventional supernatant replacement
Abcam EdU, DNA synthesis monitoring probe, 250MG
MW 252.22 Da, Purity >98%. Thymidine analog. Alternative to BrdU (5-Bromo-2'-deoxyuridine) (ab142567) for measuring de novo DNA synthesis during S-phase. Cytotoxic anti-metabolite. Used for probing short-term DNA synthesis in tissue culture and living organisms where prolonged cell survival is not required.
The product is subject to the following: Abcam Restricted Use Statement
Cayman Chemical 5-methylthIo DMT 1mg
An analytical reference standard categorized as a tryptamine; intended for research and forensic applications
Sigma Aldrich Fine Chemicals Biosciences 4,5-Dicyanoimidazole | ≥98% | Mol. Wt. 96.08 | CAS 6627-59-4 MDL MFCD00133341 | 4 x 2.5L
4,5-Dicyanoimidazole (DCI) | Purity: ≥98% | Mol Wt: 96.08 | CAS No: 6627-59-4 | MDL No: MFCD00133341 | 2.5 LDCI is an activator solution used during oligonucleotide synthesis to catalyze the coupling reaction between phosphoramidites and the growing oligonucleotide chain. This product contains 0.5 M DCI dissolved in acetonitrile. It is packaged in 4 x 2.5 L containers.
Medchemexpress LLC DMT-2′Fluoro-dU phosphoramidite | 146954-75-8 | 100.0% | C39H46FN4O8P | 1 ML
DMT-2′Fluoro-dU Phosphoramidite is a uridine phosphoramidite featuring a fluorine atom at the 2' position. This compound is suitable for nucleoside modification and the synthesis of DNA. Fluorination, a prevalent chemical derivatization in pharmaceutical chemistry, leverages fluorine's unique biophysical and biochemical properties, including its small size and high electronegativity. The ongoing research and development of novel fluorinated nucleic acid molecules are crucial for advancements in drug discovery and fundamental biochemical studies.
- Uridine phosphoramidite with fluorine at the 2' position
- Can be used for nucleoside modification
- Suitable for synthesis of DNA
- Supports innovative drug discovery
- Aids basic biochemical studies
Vector Biolabs Plasminogen activator inhibitor-2 / serpin peptidase inhibitor, clade B (ovalbumin), member 2 Adenovirus (Ad-PAI-2)
PAI-1 and PAI-2 (plasminogen activator inhibitor-1 and -2) are members of the serpin serine proteinase inhibitor family. PAI-1 and PAI-2 regulate uPA (urokinase-type plasminogen activator) and TPA (tissue plasminogen activator), resulting in the inhibition of proteolytic activity. Members of the serpin family generally complex with their target proteinases, then disassociate slowly into cleaved species that fold into stable inactive forms. PAI-1 can fold into the inactive state without cleavage resulting in the latent form of PAI-1. Activity can be restored to the latent form of PAI-1 through denaturation and renaturation. PAI-2 occurs in secreted and cytosolic forms through facultative polypeptide translocation.