Phenylcarbamic acid esters
Medchemexpress LLC Mouse CD3+ T Cells Negative Selection Kit | 1 ML
The Mouse CD3+ T Cells Negative Selection Kit is designed for the isolation of CD3+ T cells from single cell suspensions of mouse spleen cells and lymph nodes. It employs a biotin-labeled monoclonal antibody to mark non-target cells, which are subsequently removed using streptavidin-labeled magnetic beads. This user-friendly, portable kit provides high-purity cells suitable for various downstream applications.
- Enables sorting of target cells in as little as 15 minutes.
- Eliminates the need for separation columns by using a magnetic separator for swift cell separation.
- Can yield sorted cells with a purity exceeding 95%.
- Sorted cells are free of antibody and magnetic bead labeling, and retain high activity and functionality for downstream experiments.
Medchemexpress LLC N-Nornuciferine | 4846-19-9 | 1 ML
N-Nornuciferine is an aporphine alkaloid derived from lotus leaf. It is known for its significant inhibitory activity against the CYP2D6 enzyme, with IC50 and Ki values of 3.76 μM and 2.34 μM, respectively.
- Derived from lotus leaf
- Selectively inhibits CYP2D6 activity
- Shows weak or no inhibition of other P450 isoenzymes (CYP2C19, CYP3A4, CYP2E1, CYP2C9)
- Competitively inhibits dextromethorphan o-demethylation
Medchemexpress LLC N-Benzoylcytidine | 13089-48-0 | 99.5% | C16H17N3O6 | 1 ML
N-Benzoylcytidine is a modified cytidine analogue that can be phosphorylated by uracil-cytidine kinase (UCK1 and UCK2). It can be used to synthesize 2-OH protective groups for solid-phase RNA synthesis and synthetic oligonucleotides for UV induction and targeted gene silencing in zebrafish embryos.
- Modified cytidine analogue
- Can be phosphorylated by uracil-cytidine kinase (UCK1 and UCK2)
- Useful for synthesizing 2-OH protective groups for solid-phase RNA synthesis
- Can be used to synthesize oligonucleotides for UV induction and targeted gene silencing in zebrafish embryos
- For research use only
Medchemexpress LLC SULT1E1 protein, human (N-His) | >95.0% | 500 UG
Recombinant human SULT1E1 (N-His) is a purified sulfotransferase enzyme expressed in Escherichia coli and supplied as a sterile, lyophilized powder. The protein is characterized by >95% purity by reducing SDS-PAGE, is formulated from 50 mM Tris-HCl, 200 mM NaCl, pH 7.4 with 8% trehalose, and is provided in sizes suitable for biochemical assays and enzyme characterization.
- Recombinant human enzyme with N-terminal His tag
- Expressed in Escherichia coli for consistent expression yield
- Greater than 95.0% purity by reducing SDS-PAGE
- Lyophilized sterile powder for long-term storage
- Lyophilized from 50 mM Tris-HCl, 200 mM NaCl, pH 7.4, 8% trehalose
- Recommended reconstitution concentration not less than 100 μg/mL in ddH2O
Medchemexpress LLC TMEM173 Human N-Hi 500ug
Recombinant human TMEM173 (STING) protein with an N-terminal SUMO fusion and N-terminal 6xHis affinity tag, expressed in Escherichia coli and supplied as a purified research reagent for biochemical and signaling studies, including investigations of the cGAS-STING pathway.
- N-terminal SUMO and 6xHis purification tags.
- Expressed in Escherichia coli for bacterial expression.
- Supplied as purified recombinant protein for research use.
- Suitable for biochemical assays and signaling pathway studies.
- Available in a 500 μg package for assay development and characterization.
Medchemexpress LLC Phenylboronic acid | 98-80-6 | MFCD00002103 | 121.93 | 25 G
Phenylboronic acid is a biochemical reagent utilized as a biological material or organic compound for life science-related research.
- Used as a biochemical reagent
- Functions as a biological material
- Acts as an organic compound
- Suitable for life science research
- Applied in Mizuroki Heck coupling reactions
- Applied in Suzuki Miyaura coupling reactions
Aobchem 3-(N-Boc-amino)phenylboronic acid, AOBCHEM USA 10736-5G. 380430-68-2. MFCD03411945
3-(N-Boc-amino)phenylboronic acid, AOBCHEM USA 10736-5G. 380430-68-2. MFCD03411945
Medchemexpress LLC MicroRNA Antagomir N 5nmol | 5nmol
MicroRNA Antagomir Negative Control is a chemically-modified oligonucleotide (2 phosphorothioates at the 5 end 4 phosphorothioates at the 3 end 1 cholesterol group at the 3 end and full-length nucleotide 2 -methoxy modification) and can be used as a negative control The sequence of MicroRNA Antagomir Negative Control is derived from cel-mir-239b It has minimal sequence identity with miRNAs in human mouse and rat
![eMolecules Pharmablock / tert-butyl N-[[3-(aminomethyl)phenyl]methyl]carbamate / 25mg / 665627522 / PBU5082 / 0.000 / 108467-99-8 / MFCD01317800 / 236.315 / C13H20N2O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502515058.JPG-250.jpg)
eMolecules Pharmablock / tert-butyl N-[[3-(aminomethyl)phenyl]methyl]carbamate / 25mg / 665627522 / PBU5082 / 0.000 / 108467-99-8 / MFCD01317800 / 236.315 / C13H20N2O2
Pharmablock / tert-butyl N-[[3-(aminomethyl)phenyl]methyl]carbamate / 25mg / 665627522 / PBU5082 / 0.000 / 108467-99-8 / MFCD01317800 / 236.315 / C13H20N2O2
Medchemexpress LLC (4S)-1-Boc-4-fluoro-D-proline | 681128-50-7 | 97.0% | 233.24 g·mol⁻¹ | C10H16FNO4 | 25 G
(4S)-1-Boc-4-fluoro-D-proline is a Boc-protected, fluoro-substituted D-proline derivative used as a synthetic building block in organic and medicinal chemistry. It supplies a stereodefined fluorinated proline residue for incorporation into peptides and small molecules, enabling conformation control and exploration of structure-activity relationships.
- Boc-protected amino acid compatible with standard peptide coupling chemistry.
- Fluorine substitution at the 4-position to influence conformational preference and metabolic stability.
- D-configuration (4S) provides stereochemical control for peptide design.
- High chemical purity suitable for synthesis applications.
- Available in gram-scale quantities for preparative synthesis.
Medchemexpress LLC Boc-aminooxy-amide-PEG4-propargyl | 2253965-01-2 | 404.46 g/mol | C18H32N2O8 | 100 MG
Boc-aminooxy-amide-PEG4-propargyl is a Boc-protected aminooxy-containing PEG4 linker with a propargyl (alkyne) terminus. It is described as a non-cleavable, 4-unit PEG ADC linker used in conjugation and click chemistry applications.
- Non-cleavable 4-unit PEG linker.
- Contains Boc-protected aminooxy and propargyl (alkyne) functional groups.
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAC) click reactions.
- Suitable for antibody-drug conjugate (ADC) synthesis and general bioconjugation.
- Available in small research pack sizes for synthetic applications.
Medchemexpress LLC Galanin protein, human (N-His, C-Myc) | >90.0% | 50UG
Galanin protein, human (N-His, C-Myc) is a recombinant human-derived galanin fragment (residues G44-S123) provided for research applications. The protein carries an N-terminal 10xHis tag and a C-terminal c-Myc tag, is expressed in Escherichia coli, and is supplied with batch-specific documentation for characterization and quality control.
- Recombinant human galanin fragment G44-S123.
- N-terminal 10xHis and C-terminal c-Myc tags.
- Expressed in Escherichia coli for efficient production.
- Purity >90% as determined by reducing SDS-PAGE.
- Predicted molecular weight 16.4 kDa; observed ~18 kDa on SDS-PAGE.
- Batch-specific data sheet, SDS, and COA available.
Medchemexpress LLC 2-Iodoaniline | 615-43-0 | MFCD00007680 | 219.03 | 1 ML
2-Iodoaniline (2-Iodophenylamine) is an aniline derivative with potential hepatotoxic and nephrotoxic activity, intended for research use only.
- Aniline derivative
- Exhibits potential hepatotoxic activity
- Exhibits potential nephrotoxic activity
- Induces oliguria, diminished kidney weight, and tubular casts in animal models
- Decreases renal cortical slice accumulation of organic anions
- Elevates plasma ALT/GPT activity and alters morphology in the centrilobular region
- For research use only
Medchemexpress LLC N-docosanoyl taurine | 783284-48-0 | MFCD12912230 | 99.0% | 447.7 g/mol | C24H49NO4S | 1MG
N-docosanoyl taurine is a lipoamino acid (a taurine-conjugated long-chain fatty acid) reported as a discriminatory metabolite in brain-region classification. It is provided as a solid research reagent for biochemical and metabolomic studies and is characterized by CAS 783284-48-0, molecular formula C24H49NO4S, and molecular weight 447.7 g/mol.
- Lipoamino acid with taurine conjugation.
- Reported as a discriminatory metabolite in brain-region studies.
- Solid research reagent with formula C24H49NO4S.
- Molecular weight 447.7 g/mol.
- High purity suitable for analytical and biochemical research.
- Supplied in small research quantities; store at -20 °C.