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EGTA AM

(Synonyms: 3,12-双[2-[(乙酰氧基)甲氧基]-2-氧代乙基]-6,9-二氧杂-3,12-二氮杂十四烷二酸1,14-双[(乙酰氧基)甲基]酯,EGTA Acetoxymethyl ester) 目录号 : GC43589 复制 一键复制产品信息

EGTA AM是一种膜通透性的Ca2+螯合剂,具有缓慢的螯合动力学特性。

EGTA AM Chemical Structure

Cas No.:99590-86-0

规格 价格 库存 购买数量
1mg
¥1,107.00
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5mg
¥2,475.00
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10mg
¥3,555.00
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25mg
¥5,481.00
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50mg
¥7,389.00
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100mg
¥9,810.00
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Sample solution is provided at 25 µL, 10mM.

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Description

EGTA AM is a membrane-permeable Ca2+ chelator with slow chelating dynamics[1]. EGTA AM can be loaded into the cell by bath application and can therefore block the slow rise in Ca2+ required to trigger asynchronous release of glutamate [1]. Calcium chelation by EGTA AM inhibits the zona pellucida-induced acrosome reaction and apoptosis, and increases sperm motility [2]. EGTA AM can inhibit the fusion to form hybrid organelles by chelating calcium ions[3]. EGTA AM can effectively dissolve amyloid plaques in Alzheimer's disease brain tissue samples at low concentrations[4]. EGTA AM facilitates the detection of M1/MUC5AC mucin by altering the physicochemical properties of respiratory mucin, thereby exposing epitopes with which anti-M1 monoclonal antibodies are reactive[5]. EGTA AM can bind to harmful redox-active metal ions and can detoxify reactive oxygen and nitrogen substances, which is helpful for the development of catalytic antioxidants[6].

References:
[1] Li M J, Chang T W, Hung W C, et al. Cholinergic and glutamatergic transmission at synapses between pedunculopotine tegmental nucleus axonal terminals and A7 catecholamine cell group noradrenergic neurons in the rat[J]. Neuropharmacology, 2016, 110: 237-250.
[2] Ebrahimi B, Keshtgar S. The effects of EGTA on the quality of fresh and cryopreserved-thawed human spermatozoa[J]. Iranian Journal of Medical Sciences, 2020, 45(3): 188.
[3] Pryor P R, Mullock B M, Bright N A, et al. The role of intraorganellar Ca2+ in late endosome–lysosome heterotypic fusion and in the reformation of lysosomes from hybrid organelles[J]. The Journal of cell biology, 2000, 149(5): 1053-1062.
[4] Cherny R A, Legg J T, McLean C A, et al. Aqueous dissolution of Alzheimer's disease Aβ amyloid deposits by biometal depletion[J]. Journal of Biological Chemistry, 1999, 274(33): 23223-23228.
[5] Roger P, Gascard J P, Bara J, et al. EGTA treatment of human airways in vitro unmasks M1/MUC5AC mucin in submucosal glands[J]. European Respiratory Journal, 2001, 18(1): 176-183.
[6] Fisher A E O, Hague T A, Clarke C L, et al. Catalytic superoxide scavenging by metal complexes of the calcium chelator EGTA and contrast agent EHPG[J]. Biochemical and biophysical research communications, 2004, 323(1): 163-167.

EGTA AM是一种膜通透性的Ca2+螯合剂,具有缓慢的螯合动力学特性[1]。EGTA AM可通过浸浴给药的方式加载到细胞中,因此能够阻断触发谷氨酸异步释放所需的Ca2+缓慢升高[1]。EGTA AM对钙离子的螯合作用能够抑制透明带诱导的顶体反应和细胞凋亡,并提高精子活力[2]。EGTA AM可通过螯合钙离子来抑制融合形成杂交细胞器[3]。EGTA AM在低浓度下能够有效溶解阿尔茨海默病脑组织样本中的淀粉样斑块[4]。EGTA AM通过改变呼吸道黏蛋白的理化性质,从而暴露出能与抗M1单克隆抗体反应的表位,进而促进M1/MUC5AC黏蛋白的检测[5]。EGTA AM能够结合有害的氧化还原活性金属离子,并可使活性氧和活性氮物质解毒,这有助于催化性抗氧化剂的开发[6]

化学性质

Cas No. 99590-86-0 SDF
别名 3,12-双[2-[(乙酰氧基)甲氧基]-2-氧代乙基]-6,9-二氧杂-3,12-二氮杂十四烷二酸1,14-双[(乙酰氧基)甲基]酯,EGTA Acetoxymethyl ester
Canonical SMILES CC(OCOC(CN(CC(OCOC(C)=O)=O)CCOCCOCCN(CC(OCOC(C)=O)=O)CC(OCOC(C)=O)=O)=O)=O
分子式 C26H40N2O18 分子量 668.6
溶解度 DMSO : 100 mg/mL (149.57 mM; ultrasonic and warming and heat to 60°C) 储存条件 Store at -20°C
General tips 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

制备储备液
1 mg 5 mg 10 mg
1 mM 1.4957 mL 7.4783 mL 14.9566 mL
5 mM 299.1 μL 1.4957 mL 2.9913 mL
10 mM 149.6 μL 747.8 μL 1.4957 mL
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动物体内配方计算器 (澄清溶液)

第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)
给药剂量 mg/kg 动物平均体重 g 每只动物给药体积 ul 动物数量
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