Laminin Fragments

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05-23-0310 Natriuretic Peptide, C-Type, Human and Porcine - CAS 127869-51-6 - Calbiochem Member of the natriuretic peptide family that shares structural homology with ANP and plays a role in the regulation of body fluid homeostasis, vascular tone, and vascular growth.  
05-23-1200 Neurotensin - CAS 39379-15-2 - Calbiochem Potent hypothalamic peptide neurotransmitter.  
05-23-2005 Neuropeptide Y, Human - CAS 90880-35-6 - Calbiochem A potent vasoconstrictor.  
05-23-3703 Laminin Nonapeptide - CAS 110590-60-8 - Calbiochem Active in cell adhesion and cell-surface receptor binding and in stimulating cell migration.  
171596 β-Amyloid Peptide (1-42), Rat Predominant peptide found in the brain of patients with Alzheimer's Disease and Down's Syndrome. Promotes down-regulation of Bcl-2 and upregulation of Bax expression in neurons.  
343781-M ω-Conotoxin GVIA, Conus geographus - CAS 106375-28-4 - Calbiochem A neurotoxin that acts as an antagonist of voltage-activated N-type Ca2+ channels and of neurotransmitter release at neuronal synapses.  
356310 Glyburide - CAS 10238-21-8 - Calbiochem A sulfonylurea that selectively blocks ATP-sensitive K+ channels.  
420336-M KB-R7943 - CAS 182004-65-5 - Calbiochem  
422689 Kir2.1 Inhibitor, ML133 - CAS 185669-79-8 - Calbiochem The Kir2.1 Inhibitor, ML133, also referenced under CAS 185669-79-8, controls the biological activity of Kir2.1. This small molecule/inhibitor is primarily used for Cancer applications.  
445865 mGluR5 Ligand, CDPPB - CAS 781652-57-1 - Calbiochem A pyrazole amide compound that crosses the blood-brain barrier and acts as a potent, selective, reversible, positive allosteric modulator for metabotropic glutamate receptor subtype 5 (mGluR5).  
445874 mGluR5 Antagonist, MTEP - CAS 329205-68-7 - Calbiochem The mGluR5 Antagonist, MTEP, also referenced under CAS 329205-68-7, controls the biological activity of mGluR5. This small molecule/inhibitor is primarily used for Neuroscience applications.  
454575 N-Methyl-D-aspartic Acid, Hydrate - CAS 6384-92-5 - Calbiochem Excitatory amino acid neurotransmitter.  
454585 NMDA Receptor NR2BCT(1292-1304)-TAT - Calbiochem A 13-mer NMDA receptor 2B (NR2B) subunit carboxy terminal (1292-1304) derived peptide that specifically binds DAPK1 in a reversible manner and antagonizes the activated DAPK1-NR2B interaction and the potentiation of NMDAR function  
454586 NMDAR2C/2D Inhibitor, DQP-1105 - Calbiochem The NMDAR2C/2D Inhibitor, DQP-1105 controls the biological activity of NMDAR2C/2D. This small molecule/inhibitor is primarily used for Neuroscience applications.  
480026 NBD-Binding Peptide II, Cell Permeable, CTP-NBD - Calbiochem A cell-permeable cytoplasmic transduction peptide (CTP; YGRRARRRARR) fused to the NEMO binding domain peptide (NBD; TALDWSWLQTE) that acts as a potent inhibitor of TNFα-stimulated NF-κB activity (IC₅₀~ 50 µM in HCT116 cells).  
481981 Nifedipine - CAS 21829-25-4 - Calbiochem Relatively selective blocker of L-type Ca2+ channels.  
487960 Nociceptin - CAS 170713-75-4 - Calbiochem Endogenous ligand for the opioid-like G-protein coupled receptor, ORL1 (Opioid Receptor-Like 1).  
492031 NS8593 - Calbiochem An aminobenzimidazole derivative that selectively and reversibly blocks small conductance Ca2+-activated K+ channels in a Ca2+-dependent manner.  
552233 QX-314 - CAS 21306-56-9 - Calbiochem A quaternary lidocaine derivative, permanently charged, and lipophobic.  
554412 Tetrodotoxin, Citrate, Fugu sp. - CAS 18660-81-6 - Calbiochem Tetrodotoxin, Fugu sp., CAS 18660-81-6, is a reversible blocker of Na+ channels. Inhibits the release of glutamate via Na+-dependent glutamate transporter.  
557324 Riluzole - CAS 1744-22-5 - Calbiochem A cell-permeable benzothiazole compound that potently inhibits glutamate release and blocks Na+ channels.  
676950-M Veratridine - CAS 71-62-5 - Calbiochem A Na+ channel opener.  
PP69 β-Amyloid Peptide (1-42), Human  
C6171 Cys-Ser-Arg-Ala-Arg-Lys-Gln-Ala-Ala-Ser-Ile-Lys-Val-Ala-Val-Ser-Ala-Asp-Arg ≥90% (HPLC) Supports neurite outgrowth and stimulates neuronal-like process formation.