Sugar acids and derivatives
![Research Products International Corp MUG [4-Methylumbelliferyl-B-D-glucuronide Trihydrate], 1 Gram](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00006095-M65900-1.03.JPG-250.jpg)
Research Products International Corp MUG [4-Methylumbelliferyl-B-D-glucuronide Trihydrate], 1 Gram
Fluorescent substrate for β-D-Glucuronidase (GUS) encoded by the gusA gene isolated from E. coli. Fluorescence assay allows quantitation of GUS activity in protein extracts at peak excitation of 365 nm (UV) and a peak emission of 455 nm (blue).
Sigma Aldrich Fine Chemicals Biosciences 3dGROTM Colon Intestinal O
Patient derived organoids (PDOs) are novel in vitro 3D cell models that preserve original tissue physiology and molecular pathology thus representing a clinically-relevant alternative to traditional 2D cell lines and an effective tool to refine and reduce animal models. PDOs can be derived from adult patient biopsies or resected tissues containing native LGR5 stem cell populations and cultured within an ECM-rich substrate using specialized organoid media such as L-WRN conditioned media. Adult tissue derived organoids are phenotypically and genetically stable in long term culture presenting more mature phenotypes compared to iPSC-derived organoids. Importantly PDOs have shown to be able to predict patient clinical responses to chemotherapeutics.We are now offering a comprehensive biobank of highly characterized tissue-derived human gastrointestinal organoids from normal and diseased patients. The intestinal organoid biobank contains over 50 highly characterized intestinal organoids f
![Medchemexpress LLC Sar-[D-Phe8]-des-Arg9-Bradykinin | 126959-88-4 | MFCD05662308 | 100.0% | 975.10 g·mol⁻¹ | C47H66N12O11 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000244666.png-250.jpg)
Medchemexpress LLC Sar-[D-Phe8]-des-Arg9-Bradykinin | 126959-88-4 | MFCD05662308 | 100.0% | 975.10 g·mol⁻¹ | C47H66N12O11 | 10 MG
Sar-[D-Phe8]-des-Arg9-Bradykinin is a synthetic peptide agonist of the bradykinin B1 receptor used in pharmacology research to study B1-mediated vascular contractility and inflammatory signaling. It is supplied as a white to off-white solid with defined sequence and characterized physicochemical properties for in vitro applications.
- High purity (99.96%).
- White to off-white solid appearance.
- Molecular weight 975.10 g·mol⁻¹.
- Sequence: {Sar}-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe.
- CAS number 126959-88-4.
- Soluble in DMSO at 100 mg/mL; may require ultrasonic.
- Store sealed at -80°C (up to 2 years) or -20°C (up to 1 year).
- Available in multiple mg sizes (5 mg-100 mg).
![eMolecules cis-Bicyclo[3.1.0]hexan-3-ol | 694-43-9 | MFCD20921684 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502193492.JPG-250.jpg)
eMolecules cis-Bicyclo[3.1.0]hexan-3-ol | 694-43-9 | MFCD20921684 | 1g
Combi-Blocks | cis-Bicyclo[3.1.0]hexan-3-ol | 1g | 267210850 | ST-7476 | 97.000 | 694-43-9 | MFCD20921684 | 98.145 | C6H10O
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Cayman Chemical D-GlucuronIc AcId 100g
A metabolite of glucose; a component of proteoglycans; levels are increased in fibroblasts isolated from patients with ISSD or Salla disease
Apexbio Technology LLC HMP Linker 68858-21-9 100g
HMP Linker is an acid-sensitive linker used in solid-phase peptide synthesis (SPPS) It is designed to facilitate the covalent attachment of peptide carboxy-terminal residues to solid-phase resin supports and enables controlled cleavage of synthesized peptides under mildly acidic conditions thereby preserving the structural integrity of sensitive functional groups and peptide termini HMP Linker acts primarily by hydrolyzing upon acid catalysis which allows the intact release of peptides from resin supports Based on these properties HMP Linker holds research potential in peptide therapeutics synthesis and studies requiring mild peptide cleavage conditions
Medchemexpress LLC Knt-127 | 1256921-89-7 | 99.6% | 25 MG
KNT-127 is a selective, blood-brain barrier penetrant δ-opioid receptor (DOR) agonist used in neuroscience research; it preferentially activates cAMP signaling with reduced β-arrestin recruitment.
- Selective δ-opioid receptor agonist with reported Ki = 0.16 nM
- Blood-brain barrier penetrant, suitable for in vivo studies
- Biased ligand favoring cAMP signaling over β-arrestin pathways
- High reported purity (99.6%) appropriate for research applications
- Available in small pack sizes, including 25 mg
![eMolecules 3-Azabicyclo[3.1.0]hexane hydrochloride | 73799-64-1 | MFCD12197361 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502137497.JPG-250.jpg)
eMolecules 3-Azabicyclo[3.1.0]hexane hydrochloride | 73799-64-1 | MFCD12197361 | 1g
Ambeed | 3-Azabicyclo[3.1.0]hexane hydrochloride | 1g | 525876724 | A144626 | | 73799-64-1 | MFCD12197361 | 119.590 | C5H10ClN
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