Custom Purified Nucleic Acids
Invitrogen™ ViewRNA™, 120 μL
This is a customizable probe set for the ViewRNA ISH Cell, ViewRNA ISH Tissue, and ViewRNA Cell Plus assays.
Invitrogen™ ViewRNA™ microRNA, 120 μL
This is a customizable microRNA probe set for the ViewRNA ISH Cell, ViewRNA ISH Tissue, and ViewRNA Cell Plus assays.
Invitrogen™ ViewRNA™ microRNA, 440 μL
This is a customizable microRNA probe set for the ViewRNA ISH Cell, ViewRNA ISH Tissue, and ViewRNA Cell Plus assays.
Medchemexpress LLC Efgartigimod alfa | 1821402-21-4 | 99.5% | 10MG
Efgartigimod alfa is an anti-neonatal Fc receptor (FcRn) IgG1 Fc fragment supplied as a research reagent for studying FcRn-mediated IgG recycling and autoimmune conditions such as myasthenia gravis. The material is provided as a purified recombinant protein with analytical characterization for in vitro and preclinical research use.
- High purity (99.47% by SEC-HPLC) for reproducible results.
- Characterized molecular weight (51.28 kDa) to support analytical assays.
- Validated for FcRn/Fc receptor research applications.
- Supplied in small-scale quantities suitable for laboratory studies.
- Accompanied by product datasheet and batch-specific COA.
Medchemexpress LLC Elebsiran sodium (VIR-2218 sodium) | 00-00-0 | 95.8% | C485H658F9N158O294P39S6 | 10MG
Elebsiran sodium is a research-grade small interfering RNA (siRNA) sodium salt designed to target and degrade hepatitis B virus (HBV) and hepatitis D virus (HDV) RNA transcripts. It is GalNAc-conjugated for liver-targeted delivery and is intended for laboratory research into antiviral activity and antigen reduction.
- Targets HBV and HDV RNA transcripts for RNAi-mediated degradation.
- GalNAc conjugation enables liver-targeted delivery via ASGPR.
- Demonstrates reduction of HBsAg and viral load in studies.
- Provided as the sodium salt suitable for in vitro and in vivo research.
- High purity appropriate for biological assays (95.8%).
Medchemexpress LLC Xl888 | 1149705-71-4 | MFCD22124888 | 99.4% | C29H37N5O3 | 10MG
XL888 is an orally bioavailable, ATP-competitive small-molecule inhibitor of heat shock protein 90 (HSP90) used in oncology research. It destabilizes HSP90 client proteins, leading to cell cycle arrest and apoptosis, and has demonstrated anti-proliferative and anti-tumor activity in preclinical studies. Reported biochemical potency against HSP90 is ~24 nM.
- Orally bioavailable small-molecule suitable for in vivo and in vitro studies.
- ATP-competitive mechanism that targets HSP90 chaperone activity.
- Demonstrated anti-proliferative and pro-apoptotic effects in cancer cell lines.
- Reported low nanomolar biochemical potency in cell-free assays.
- Useful for pharmacology and mechanism-of-action studies involving HSP90 clients.
Medchemexpress LLC Bizelesin | 129655-21-6 | MFCD00892028 | 95.1% | 815.70 g·mol⁻¹ | C43H36Cl2N8O5 | 5 MG
Bizelesin is an AT-specific DNA alkylating agent that generates DNA interstrand crosslinks and inhibits DNA replication, used in preclinical research to evaluate anticancer activity.
- AT-specific DNA alkylating activity.
- Generates DNA interstrand crosslinks.
- Effectively inhibits DNA replication.
- Off-white to gray solid with high purity (~95%).
- Soluble in DMSO; formulation guidance available for in vivo use.
- Stable in solvent at -80°C for 6 months and at -20°C for 1 month when protected from light.
Medchemexpress LLC Nampt-IN-10 (TFA) | 2567724-20-1 | 98.6% | C27H28FN5O2·C2HF3O2 | 10MG
Nampt-IN-10 TFA is the trifluoroacetate salt of a potent nicotinamide phosphoribosyltransferase (NAMPT) inhibitor provided for research use; it exhibits cellular activity and is supplied at high purity for in vitro and preclinical studies.
- Trifluoroacetate salt form for improved handling and solubility
- High purity (98.6%) suitable for sensitive assays
- Demonstrated cellular potency in cancer cell lines
- Supplied in multiple pack sizes to suit experimental needs
- For research use only; not for clinical or diagnostic use
Medchemexpress LLC Aluminum phthalocyanine chloride | 14154-42-8 | MFCD00049386 | 85.0% | 574.96 g/mol | C32H16AlClN8 | 5 MG
Aluminum phthalocyanine chloride is a photosensitizing phthalocyanine dye used in photodynamic therapy research and fluorescence studies. It is a chloroaluminum complex with strong absorption in the red region and is supplied as a research-grade solid with supporting documentation for laboratory use.
- Photosensitizer with strong absorption in the red region.
- Suitable for photodynamic therapy and fluorescence research applications.
- Available in research-scale pack sizes for small-batch experiments.
- Provided with safety data sheet and certificate of analysis for safe handling.
- Stable solid form for storage and experimental reproducibility.
Expression Systems BestBac 1.0 Linearized Baculovirus DNA
Expression Systems’ popular BestBac Linearized Baculovirus DNA backbone has been engineered to deliver highly efficient recombination with all polyhedron gene locus based transfer vectors. The resulting virus vector provides superior stability and purity compared to other systems.
• Unmatched productivity and stability for BEVS
• Improved production methodology can reduce need for plaque purification
Produces high titers of 5 E8 to 3 E9 IU/ml of recombinant baculovirus in P1 stock
• Generates P1 stock as quickly as Bac-to-Bac® and other systems
• Each BestBac vial contains enough material for a minimum of five cotransfections
• Suitable for other expression systems including BacMam™
• BestBac 1.0 is wild type at the cathepsin and chitinase (v-cath/chiA) loci, preferred for some applications.
Medchemexpress LLC Vegfr2-in-2 | 737818-56-3 | 99.3% | C15H11BrN2O | 10MG
VEGFR2-IN-2 is a potent and selective VEGFR2 inhibitor (compound 6e) reported with an IC50 of 19.32 nM and intended for laboratory research into angiogenesis and oncology. The material is supplied as a solid with supporting SDS and COA documents available for verification.
- Potent VEGFR2 inhibitor with IC50 = 19.32 nM.
- High reported purity of 99.3% (COA).
- Solid; white to off-white appearance.
- Molecular formula C15H11BrN2O, molecular weight 315.16.
- Available in small-scale quantities (1 mg-100 mg) and as a 10 mM solution.
- SDS and certificate of analysis available for verification.
- Intended for in vitro research use only; not for human or veterinary use.
Medchemexpress LLC Bobcat339 | 2280037-51-4 | 99.4% | 297.74 g·mol⁻¹ | C16H12ClN3O | 5 MG
Bobcat339 is a cytosine-based small-molecule inhibitor of TET enzymes used in epigenetic research. It inhibits TET1 and TET2 with reported IC50 values of 33 μM and 73 μM, and is provided in milligram quantities for laboratory studies.
- Cytosine-based inhibitor of TET enzymes.
- Reported IC50 values: 33 μM for TET1 and 73 μM for TET2.
- High purity (99.44%) suitable for research applications.
- Available in multiple milligram-scale packaging for experimental flexibility.
- Useful for studying DNA demethylation and epigenetic regulation.
- Datasheet available with chemical, physical, and handling information.
![Medchemexpress LLC 1-[6-(4-azido-2-nitroanilino)hexanoyloxy]-2,5-dioxopyrrolidine-3-sulfonic acid | 102568-43-4 | MFCD00054986 | 99.8% | C16H18N6O9S | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000259404.png-250.jpg)
Medchemexpress LLC 1-[6-(4-azido-2-nitroanilino)hexanoyloxy]-2,5-dioxopyrrolidine-3-sulfonic acid | 102568-43-4 | MFCD00054986 | 99.8% | C16H18N6O9S | 10MG
Sulfo-SANPAH is a heterobifunctional, water-soluble cross-linker combining a sulfo-NHS ester with a photoreactive nitrophenylazide. It reacts with primary amines and, after UV activation, forms covalent bonds to nearby substrates, making it suitable for immobilizing proteins and extracellular matrix components on polymer surfaces and hydrogels. Supplied as an orange-red solid with recommended frozen storage for long-term stability.
- Heterobifunctional cross-linker with amine-reactive sulfo-NHS ester.
- Photoactivatable nitrophenylazide enables UV-triggered covalent coupling.
- Water-soluble for direct use in aqueous buffers.
- Enables covalent immobilization of proteins and ECM to substrates.
- Supplied as a solid powder with stable storage at frozen temperatures.
- High purity for consistent conjugation performance.
Medchemexpress LLC Basroparib | 1858179-75-5 | 98.6% | C18H21F2N7O3 | 10MG
Basroparib is a small-molecule poly(ADP-ribose) polymerase (PARP) inhibitor supplied for research use. It is used in biochemical and cellular studies to probe DNA damage response and PARP-related mechanisms. The compound is provided as a powder with reported purity of 98.64%, molecular formula C18H21F2N7O3, and CAS 1858179-75-5.
- Selective inhibition of PARP activity for mechanistic studies.
- Suitable for in vitro biochemical and cellular assays.
- High reported purity supports analytical and assay reproducibility.
- Stable powder form for storage and handling convenience.
- Characterized by molecular formula C18H21F2N7O3.
Medchemexpress LLC Propamidine isethionate | 140-63-6 | MFCD01728620 | 95.7% | 564.63 g/mol | C21H32N4O10S2 | 5 MG
Propamidine isethionate is a diamidine-class research reagent supplied as the isethionate salt and used primarily in laboratory studies such as Acanthamoeba keratitis research. It is provided as a high-purity solid intended for experimental use.
- Diamidine-class compound used in antiparasitic research.
- Applicable to Acanthamoeba keratitis research.
- Purity approximately 95.7%.
- Molecular weight 564.63 g/mol.
- Chemical formula C21H32N4O10S2.
- White to off-white solid appearance.
- Store sealed at 4°C; in solution store at -80°C (up to 6 months) or -20°C (up to 1 month).
- Available in small milligram quantities for laboratory use.