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Discovery Antibodies/(RS)-(Tetrazol-5-yl)glycine/50 mg/T-205-50 mg

价格
¥11940.00
货号:T-205-50mg
浏览量:127
品牌:Discovery
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商品描述
Cat#:T-205
AlternativeNameTet-glycine,Tetrazolylglycine,Tetrazol-5-yl-gly,5-Tetrazolyl-glycine,LY285265
  • LyophilizedPowder
  • BioassayTested
  • SourceSynthetic
    MW:143.1
    Purity:>98%
    Effectiveconcentration0.1-25µM.
      • (RS)-(Tetrazol-5-yl)glycine
    Chemicalname2-amino-2-(2H-tetrazol-5-yl)aceticacid.
    MolecularformulaC3H5N5O2.
    CASNo.:138199-51-6.
    PubChemCID126383
    Activity(RS)-(Tetrazol-5-yl)glycineisahighlypotentandselectiveNMDAreceptoragoNIST(significantlymorepotentthanNMDAorglutamate),inhibiting[3H]glutamatebindingtoratbrainNMDAreceptorswithIC50of36nM1.invitro,itactivatesNR1/NR2ANMDAreceptorswithEC50of1.77µM2.
      • Schoepp,D.D.etal.(1991)Eur.J.Pharmacol. 203,237.
      • Chen,P.E.etal.(2005)Mol.Pharmacol.67,1470.
    ShippingandstorageShippedatroomtemperature.Productassuppliedcanbestoredintactatroomtemperatureforseveralweeks.Forlongerperiods,itshouldbestoredat-20°C.
    SolubilitySolubleupto25mMinwater,withgentleheating.Centrifugeallproductpreparationsbeforeuse(10000xg5min).
    StorageofsolutionsStoreat-20°C.Itisrecommendedtopreparefreshsolutionsbeforeuse,oraliquotstocksolutionsstoredat-20°C.Preventrepeatedthawing.
      • (RS)-(Tetrazol-5-yl)glycine
        AlomoneLabs(RS)-(Tetrazol-5-yl)glycineactivatesNMDAreceptorsexpressedinXenopusoocytes.
        A.RepresentativetimecourseofNR1/NR2Acurrentactivationby3.5minapplicationsof0.4μM,2μMand10μM(RS)-(Tetrazol-5-yl)glycine(#T-205),asindicated,inthepresenceof50μMglycine(topdottedline),atmembraneholdingpotentialof-60mV.B.RepresentativecurrenttracesofNR1/NR2A,elicitedbytransientstimulationswithcontrolandwith10µMand25µM(RS)-(Tetrazol-5-yl)glycine(asindicated),inthepresenceof10μMglycine,whilemembranepotentialwasheldat-60mV.
    References-Scientificbackground
    • 1.Schoepp,D.D.etal.(1991)Eur.J.Pharmacol. 203,237.
    • 2.Black,S.A.etal.(2014)Front.CellDev.Biol.2,45.
    • 3.Chen,P.E.etal.(2005)Mol.Pharmacol.67,1470.
      • (RS)-(Tetrazol-5-yl)glycineisasyntheticcompoundthatactsashighlypotentandselectiveN-methyl-D-aspartate(NMDA)receptoragonist.ThecompoundissignificantlymorepotentthanNMDAorglutamate.Whengiventoneonatalrats,(RS)-(Tetrazol-5-yl)glycinewasfoundtobehighlypotentconvulsant1.

        NMDAreceptorsareheterotetramericchannelsformedbytheassemblyoftwoobligatoryGluN1andtwoGluN2/GluN3subunits.Theyplayanimportantroleinavarietyofcellularprocessesandbrainfunctionssuchassynapticplasticity,addiction,andstroke.Theyalsomediatephysiologicalfunctionssuchaslearningandmemoryformationandparticipateinglutamateexcitotoxicity2.

        (RS)-(Tetrazol-5-yl)glycineinhibits[3H]glutamatebindingtoratbrainNMDAreceptorswithanIC50valueof36nM1.invitrostudiesshowthat(RS)-(Tetrazol-5-yl)glycinecanactivateNR1/NR2ANMDAreceptorswithanEC50valueof1.77µM3.

    TargetNMDAreceptors
    receivea5mgfreetrialsample!
    Lastupdate:24/09/2019

    (RS)-(Tetrazol-5-yl)glycine(#T-205) isahighlypure,synthetic,andbiologicallyactivecompound.

    Forresearchpurposesonly,notforhumanuse
    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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