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Discovery Antibodies/Tropicamide/250 mg/T-120-250 mg

价格
¥820.00
货号:T-120-250mg
浏览量:127
品牌:Discovery
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商品描述
Cat #: T-120
Alternative Name Mydriacyl®
  • Lyophilized Powder
  • Bioassay Tested
  • Source Synthetic
    MW: 284.3
    Purity: >96%
    Effective concentration 10 nM - 100 µM.
      • Tropicamide
    Chemical name N-Ethyl-3-hydroxy-2-phenyl-N-(pyridinylmethyl)propanamide.
    Molecular formula C17H20N2O2.
    CAS No.: 1508-75-4.
    Activity Tropicamide is a muscarinic receptor (mAChR) antagonist, which shows a 3 fold selectivity for M4 over other muscarinic receptors1-2. Tropicamide inhibits porcine intravesical ureter contraction with pIC50 of ~7.53.
      • Liao, C.F. et al. (1989) J. Biol. Chem. 264, 7328.
      • Lazareno, S. et al. (1990) Br. J. Pharmacol. 109, 1120.
      • Hernandez, M. et al. (1993) Br. J. Pharmacol. 110, 1413.
    Shipping and storage Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C.
    Solubility DMSO. Centrifuge all product preparations before use (10000 x g 5 min).
    Storage of solutions Up to four weeks at 4°C or three months at -20°C.
      • Tropicamide
        Alomone Labs Tropicamide inhibits carbachol’s effect on M1 mAChR expressed in C6 cells.
        Cells were loaded with Fluo-3 AM and changes in intracellular Ca2+ were detected via changes in Fluo-3 emission. A. Normalized fluorescence before and after application (at 20 seconds, see arrow) of 10 μM Carbachol following a 20 min incubation with 0-100 μM Tropicamide (#T-120) (as indicated). B. Inhibition (as percent of control) of 10 µM Carbachol evoked Ca2+ rise, plotted against Tropicamide concentrations.
    References - Scientific background
    • 1. Bonner, T.I. et al. (1989) Trends. Neurosci. 12, 148.
    • 2. Felder, C.C. et al. (1995) FASEB. J. 9, 619.
    • 3. Bonner, T.I. et al. (1987) Science 237, 527.
    • 4. Peralta, E.G. et al. (1987) EMBO J.  6, 3923.
    • 5. Bonner, T.I. et al. (1988) Neuron 1, 403.
    • 6. Liao, C.F. et al. (1989) J. Biol. Chem. 264, 7328.
    • 7. Liao, C.F. et al. (1989) J. Biol. Chem. 264, 7328.
    • 8. Lazareno, S. et al. (1990) Br. J. Pharmacol. 109, 1120.
    • 9. Hernandez, M. et al. (1993) Br. J. Pharmacol. 110, 1413.
    • 10. Manny, R.E. et al. (2001) Invest. Ophtalmol. Vis. Sci. 42, 1728.
      • Muscarinic acetylcholine receptors (mAChR) regulate a number of important basic physiologic functions including heart rate, motor and sensory control and more complex behaviors including arousal, memory, and learning. Loss of muscarinic receptor number or function has been implicated in the etiology of several neurological disorders including Alzheimer"s dementia, Down"s syndrome and Parkinson"s disease.

        Five subtypes of muscarinic receptors (m1-m5) have been identified by molecular cloning1 and much has been learned about their distribution, pharmacology, and structure2-6.

        Tropicamide is a muscarinic receptor antagonist, which shows a 3 fold selectivity for m47-8. Its effect has a pIC50 of ~7.5 for porcine intravesical ureter contraction9.

        Tropicamide produces short acting mydriasis (dilation of the pupil) and cycloplegia (paralysis of the ciliary muscle) when applied as eye drops. It is also an effective cycloplegic agent in myopic children10.

    Target M1-M5 muscarinic receptors
    receive a 250 mg free trial sample!
    Last update: 26/09/2019

    Tropicamide (#T-120) is a highly pure, synthetic, and biologically active compound.

    For research purposes only, not for human use
    Discovery Antibodies的Cyclin dependant kinase 2 (CDK2) is a serine/threonine protein kinase which controls both G1/S and G2/M transitions. CDKs along with cyclins and CDK inhibitors regulate cell cycle progression. Specific cyclins activate different CDKs; in early G1, CDK2 pairs with cyclin E to promote entry into the S phase before switching to partner with cyclin A to drive the cell through S phase. Once activated CDKs phosphorylate downstream proteins to initiate signalling cascades. CDK2 phosphorylates and inactivates the RB1 (pRb) tumour suppressor family of proteins.CDK的活动受到严格控制。CDK2活性可以被包括P21在内的一系列抑制剂抑制。细胞周期失调和增殖控制的丧失与细胞转化和癌症密切相关。CDK2在DNA损伤反应(DDR)中的细胞周期停滞中也似乎起着积极作用,它的抑制作用会阻碍DDR,并使细胞对电离辐射敏感,从而诱导细胞死亡。该抗体与AlexaFluor®488偶联。AlexaFluor®488是一种流行的鲜绿色荧光染料,具有高pH稳定性。
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