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Nonivamide

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  • ¥600 - 3200
  • 上海莼试
  • CS-01Y74072
  • 国产
  • 2025年07月05日
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    • 详细信息
    • 技术资料
    • 库存

      25

    • 英文名

      Nonivamide

    • CAS号

      2444-46-4

    • 供应商

      上海莼试

    • 保存条件

      Store at -20°C

    • 规格

      1mg

    产品描述:
    分子式:C17H27NO3

    产品细节图片1
    分子量:293.4
    溶解度:0.1 M Na2CO3: 1 mg/ml,DMF: 15 mg/ml,DMSO: 13   mg/ml,Ethanol: 31 mg/ml
    储存条件:Store at -20°C
    General tips:For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the   ultrasonic bath for a while.
    Shipping Condition:Evaluation sample solution : ship with blue ice All other available size: ship with RT , or   blue ice upon request                                      
    Nonivamide is a agonist, which exhibits 4d-EC50 value of 5.1 mg/L in static toxicity tests.Nonivamide, a synthetic derivate of natural capsaicin, has an effective antifouling activity. Capsaicin exhibits 4d-EC50 values of 5.5±0.5 mg/L, 23±2 mg/L, 6.9±0.2 mg/L, and 15.6±0.4 mg/L in static toxicity tests conducted using Pseudomonas putida, Lake Erie bacteria, Vibrio natriegens, and Vibrio parahaemolyticus, respectively. A significant growth inhibitory effect (p<0.01) is orved in the group treated with 1 mg/L of Nonivamide for 4 d, and the EC50 value (4 d-EC50) is 5.1 mg/L[1]. Nonivamide treatment causes calcium release from the ER and altered the transcription of growth arrest- and DNA damage-inducible transcript 3 (GADD153), GADD45α, GRP78/BiP, ATF3, CCND1, and CCNG2) in a manner comparable with prototypical ER stress-inducing agents. ER calcium flux is evaluated by pretreating cells with 2.5 μM thapsigargin for 5 min followed by addition of 2.5 μM Nonivamide. Treatment of TRPV1-overexpressing cells with 2.5 μM Nonivamide produces marked increases in cytosolic calcium due to release of calcium from ER stores. Treatment of TRPV1-overexpressing cells with 1 μM Nonivamide causes an approximate 50% loss in cell viability after a 24-h period. BEAS-2B cells treated with 100 and 200 μM Nonivamide also exhibits a shift in the relative amount of EIF2α-P and an increase in the expression of GADD153 mRNA and protein[2]. Treatment with Nonivamide reduces lipid accumulation to a similar extent as CAP; the effects are not different from the effects after CAP treatment at any of the tested concentrations. Compared to untreated control cells, treatment with Nonivamide decreases lipid accumulation by 5.34±1.03% (P<0.05) at 0.01 µM up to 10.4±2.47% (P<0.001) at 1 µM[3].
    商品属性:
    货号CS-01Y74072规格1mg
    CAS号2444-46-4分子量293.4
    含量>98.00%别名N/A
    分子式C17H27NO3化学名(Z)-N-(4-hydroxy-3-methoxybenzyl)nonanimidic acid
    产地国产用途仅供科研研究实验
    注意事项:
    抗逆滴加序列
    每次向板内滴加抗原时,移液器滴头要与平面45度悬空,不要触碰到孔内的液体,由后向前依次滴加(即浓度由低往高滴加)。
    抗感染反应期
    抗原抗体在室温20~25℃下,必须反应30min以上,若环境温度低于室温,可将微量反应板置于恒温培养箱中,使二者充分反应。
    旅游温度
    磷酸盐缓冲液的pH值要在高压灭菌后进行滴定,往往在高压后pH值会有所改变,所以高压后再调一次pH值更为准确。磷酸盐缓冲液一经使用保存期不要超过3周。当pH<5.8时,红细胞会产生自凝现象;当pH>7.8时,图形洗脱加快,易造成肉眼观察产生误差;p H=7.2时,红细胞沉降最充分,图形最清晰。
    当滴注 1%红细胞悬液时,应经常摇晃红细胞悬液,使红细胞均匀地分布在磷酸缓冲液中,以防止红细胞下降。
    反应时间及温度
    加入鸡红血球之后,反应板在室温(20~25℃)静置30~40min,对照孔血球下沉于孔底,即可判定结果。若室温达不到实验要求,需相应调整反应时间。当环境温度低于4℃时,红细胞发生自凝;高于37℃时,会发生反应物分离和红细胞溶血。
    公司正在出售的产品:
    Recombnant Human MCEE, N-HSPAST Antibody Blocking Peptide
    Recombinant Human CHAC2Recombinant Acyl Coenzyme A Synthetase Long Chain Family, Member 3 (ACSL3)
    PCBP1 Antibody Blocking PeptideRecombinant Proteasome Subunit Beta Type 4 (PSMb4)
    ADAM15 Antibody Blocking PeptideRecombinant Testis Specific Kinase 2 (TESK2)
    HSF1 Antibody Blocking PeptideRecombinant Phosphatidic Acid Phosphatase Type 2C (AP2C)
    UBE2Q1 Antibody Blocking PeptideRecombinant Asparaginyl tRNA Synthetase 2, Mitochondrial (NARS2)
    CRACDL Antibody Blocking PeptideRecombinant Esterase D (ESD)
    FIBP Antibody Blocking Peptide磷酸化信号转导和转录激活因子3封闭多肽
    phospho-CDK6 (Tyr13) Antibody Blocking PeptideRecombinant Hydroxyacylglutathione Hydrolase (HAGH)
    UBAP1 Antibody Blocking PeptideRecombinant Protein Arginine Methyltransferase 1 (PRMT1)
    Influenza A Polymerase basic protein 2 Antibody Blocking PeptideRecombinant Histidyl tRNA Synthetase 2, Mitochondrial (HARS2)
    ZFP72 Antibody Blocking PeptideRecombinant Isoleucyl tRNA Synthetase 2, Mitochondrial (IARS2)
    P2Y2R Antibody Blocking PeptideNonivamideRecombinant Fatty Acid Hydroxylase (FAAH)
    NKAIN4 Antibody Blocking PeptideRecombinant Acyl Coenzyme A Dehydrogenase, Short/Branched Chain (ACADSB)
    EXOC7 Antibody Blocking PeptideRecombinant Fucosyltransferase 2 (FUT2)
    使用方法:
    1.本蛋白酶抑制剂混合物为100×的储存液,使用时按照1:100的比例加入到裂解液中(例如,1ml裂解液中加入10μl蛋白酶抑制剂混合物),混匀后即可使用。根据需要,0.5M的EDTA也按照1:100的比例加入到裂解液中(如用于检测金属蛋白酶活性,则不宜添加EDTA)。含有蛋白酶抑制剂混合物的裂解液宜现用现配,不宜配制后冻存待后续使用。
    2. 待所需的抑制剂添加完毕混匀后,就可以开始进行哺乳动物组织的裂解和蛋白提取。


     

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