Isothiocyanates
Medchemexpress LLC Mito-TEMPO | 1334850-99-5 | 99.2% | 510.03 | 1 ML
Mito-TEMPO is a mitochondria-targeted superoxide dismutase mimetic with superoxide and alkyl radical scavenging properties. It significantly reduces the increase in ALT activities and areas of necrosis, indicating sustained protection during acetaminophen-induced hepatotoxicity. Mito-TEMPO can also induce secondary apoptosis in the late phase of APAP hepatotoxicity by inhibiting RIP3.
- Mitochondria-targeted
- Superoxide dismutase mimetic
- Superoxide and alkyl radical scavenging properties
- Attenuates increases in ALT activities and reduces necrosis areas in acute liver injury
- Induces secondary apoptosis in APAP hepatotoxicity via RIP3 inhibition
Sigma Aldrich Fine Chemicals Biosciences FLUORESCEIN ISOTHIOCYANA 500MG
Fluorescein isothiocyanate isomer I, 500mg, 3326-32-7
Medchemexpress LLC 3-acetylphenyl acetate | 2454-35-5 | MFCD00017227 | 99.9% | 178.19 g/mol | C10H10O3 | 5 G
3-Acetylphenyl acetate is an aromatic acetyl ester used as a pharmaceutical intermediate and research reagent. It has the molecular formula C10H10O3 and a molecular weight of 178.19 g/mol, and is supplied at high purity for laboratory synthesis and development.
- High purity suitable for research applications.
- Useful as a pharmaceutical intermediate in organic synthesis.
- Defined molecular formula C10H10O3 and molecular weight 178.19 g/mol.
- Available in small pack sizes for laboratory use.
- Typically supplied with a certificate of analysis and safety data sheet.
Medchemexpress LLC 1-Piperidinyloxy, 4-azido-2,2,6,6-tetramethyl- | 63697-61-0 | C9H17N4O | 25 MG
N3-TEMPO is a click chemistry reagent containing an azide group. It can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups, and ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. Click chemistry is utilized in many research fields due to its high yield, high specificity, and simplicity, and has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules.
- Contains an azide group
- Undergoes copper-catalyzed azide-alkyne cycloaddition with alkyne groups
- Undergoes ring strain-promoted alkyne-azide cycloaddition with DBCO or BCN groups
- Utilized for high yield, high specificity, and simplicity in click chemistry
- Potential for binding between nucleic acids, lipids, proteins, and other molecules
Medchemexpress LLC Cyclopentyl phenyl ketone | 5422-88-8 | MFCD00001378 | 98.4% | 174.24 g/mol | C12H14O | 25 G
Cyclopentyl phenyl ketone is an organic synthesis intermediate used as a building block in medicinal chemistry and related research. It is a ketone (CAS 5422-88-8) with molecular formula C12H14O and a molecular weight of 174.24 g/mol. Supplied as a liquid with high reported purity, the compound is intended for research and synthesis applications; safety data and analytical documentation are available.
Medchemexpress LLC Rat IgG1 kappa Isot 10mg | 10mg
Rat IgG1 kappa Isotype Control a rat monoclonal antibody is an isotype control for Rat IgG1 antibody
Apexbio Technology LLC Rhodamine B isothiocyanate 36877-69-7 50mg
Rhodamine B isothiocyanate (RBITC) is a fluorescent dye bearing an isothiocyanate functional group enabling its covalent conjugation specifically to amino groups in proteins and peptides Upon excitation by green light wavelengths this compound emits characteristic orange-red fluorescence allowing for visualization and detection of labeled biomolecules in cellular and tissue samples Due to its stable covalent binding to target proteins RBITC is employed extensively in fluorescence microscopy immunohistochemical analysis and in vitro labeling studies in disciplines such as cell biology neuroscience and immunology Its chemical structure facilitates selective attachment aiding the detailed investigation of cellular localization protein dynamics and molecular interactions in biological systems
eMolecules Chem-Impex Fluorescein isothiocyanate isomer I 250mg 112440714 00860 0 000 3326-32-7 MFCD00005063 389 380 C21H11NO5S
Chem-Impex Fluorescein isothiocyanate isomer I 250mg 112440714 00860 0 000 3326-32-7 MFCD00005063 389 380 C21H11NO5S
Sigma Aldrich Fine Chemicals Biosciences 3-(Methylthio)propyl isothiocyanate >=98%, FG | 505-79-3 | MFCD00209521 | 25G
3-(Methylthio)propyl isothiocyanate >=98%, FG | Purity: >=98% | Mol Wt: 147.26 | 505-79-3 | MFCD00209521 | 25G
Sigma Aldrich Fine Chemicals Biosciences 3-(Methylthio)propyl isothiocyanate >=98%, FG | 505-79-3 | MFCD00209521 | 100G
3-(Methylthio)propyl isothiocyanate >=98%, FG | Purity: >=98% | Mol Wt: 147.26 | 505-79-3 | MFCD00209521 | 100G
Sigma Aldrich Fine Chemicals Biosciences 3-(Methylthio)propyl isothiocyanate >=98%, FG | 505-79-3 | MFCD00209521 | 1KG
3-(Methylthio)propyl isothiocyanate >=98%, FG | Purity: >=98% | Mol Wt: 147.26 | 505-79-3 | MFCD00209521 | 1KG
Sigma Aldrich Fine Chemicals Biosciences Fluorescein isothiocyanate5G
Dextran is a polymer of anhydroglucose. It is composed of approximately 95% alpha-D-(166) linkages. The remaining (163) linkages account for the branching of dextran. Conflicting data on the branch lengths implies that the average branch length is less than three glucose units. However other methods indicate branches of greater than 50 glucose units exist. Native dextran has been found to have a molecular weight (MW) in the range of 9 million to 500 million. Lower MW dextrans will exhibit slightly less branching and have a more narrow range of MW distribution. Dextrans with MW greater than 10 000 behave as if they are highly branched. As the MW increases dextran molecules attain greater symmetry. Dextrans with MW of 2 000 to 10 000 exhibit the properties of an expandable coil. At MW below 2 000 dextran is more rod-like. The MW of dextran is measured by one or more of the following methods low angle laser light scattering size exclusion chromatography copper-complexation and anthr
Medchemexpress LLC Rat IgG1 kappa Isot 1mg | 1mg
Rat IgG1 kappa Isotype Control a rat monoclonal antibody is an isotype control for Rat IgG1 antibody