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- 保存条件:
常温
- 保质期:
根据瓶身LOT号查询
- 英文名:
HEPES
- 库存:
有现货
- 供应商:
浙江羽翔生物科技有限公司
- CAS号:
7365-45-9
- 规格:
100G
属性
等级
BioPerformance Certified
质量水平
400
检测方案
≥99.5% (titration)
形式
crystalline powder
储存条件
dry at room temperature
技术
cell culture | mammalian: suitable
competitive inhibition ELISA: suitable
杂质
endotoxin and total aerobic microbial count, tested
颜色
white
有效pH范围
6.8-8.2
pKa (25 °C)
7.5
痕量阳离子
Fe: ≤5 ppm
吸光度
≤0.05 at 260 in H2O at 0.1 M
≤0.05 at 280 in H2O at 0.1 M
适用性
suitable for Western blot
suitable for component for culture media
应用
clinical research
diagnostic assay manufacturing
general analytical
life science and biopharma
异质活性
DNase, RNase, NICKase, protease, none detected
SMILES字符串
OCCN1CCN(CC1)CCS(O)(=O)=O
InChI
1S/C8H18N2O4S/c11-7-5-9-1-3-10(4-2-9)6-8-15(12,13)14/h11H,1-8H2,(H,12,13,14)
InChI key
JKMHFZQWWAIEOD-UHFFFAOYSA-N
一般描述
HEPES 在各种生物和生化过程中也被证明很有用。它的两性性使它适合作为在等电聚焦中产生 pH 梯度的分离器,这是一种经常用于蛋白质分离和分析的技术。此外,与三磷酸腺苷等取代胺基较少的缓冲液相比,HEPES 对 DNA 限制性内切酶反应的干扰最小。这使得它成为涉及 DNA 操作和分析的应用的技术。除了这些特定的应用之外,HEPES 在许多其他生物和生化过程中也很有价值,包括免疫沉淀、细胞裂解和活细胞成像。HEPES 的多功能性,加上卓越的 pH 缓冲能力和与其他分子的最小相互作用,使其成为各种研究领域不可或缺的工具。
应用
- 对Dulbecco′s modified Eagle′s medium(DMEM)培养基进行补充以培养和维持细胞系
- 作为血小板悬浮缓冲液的一种组分
- 对Hank碱性盐溶液进行补充以用于洗涤胰腺组织
- 作为在酶联免疫吸附测定(ELISA)中蛋白纯化和定量的洗涤缓冲液和封闭缓冲液中一种组分
- 生物学溶液的pH调整和维持
- 作为Hank平衡盐溶液(HBSS)和解离培养基中的一种组分用于研究神经发育
- 用于组织匀浆以及来自细胞的溶质和核提取物的制备
- 作为角质形成细胞和成纤维细胞培养基的一种组分
特点和优势
- 经过测试,确认低水平的重金属污染,确保各种应用的适用性
- 25°C 时,极易溶于水,pH 值范围为6.8 - 8.2,pKa 为 7.5
- 金属离子结合可忽略
- 与三磷酸腺苷和磷酸盐等其他缓冲剂相比,对细胞的毒性较小
- 在宽 pH 范围内稳定
- 经过测试,确定内毒素和总需氧微生物计数
- 不含 DNase, NICKase、RNase、内切酶、外切酶和蛋白酶
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文献和实验Nanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis: optimization using a full factorial design.
Nanoemulsions are drug delivery systems that may increase the penetration of lipophilic compounds through the skin, enhancing their topical effect. Chalcones are compounds of low water solubility that have been described as promising molecules for the treatment of cutaneous leishmaniasis (CL). In this context, the aim of this work was to optimize the development of a nanoemulsion containing a synthetic chalcone for CL treatment using a 2(2) full factorial design. The formulations were prepared by spontaneous emulsification and the experimental design studied the influence of two independent variables (type of surfactant - soybean lecithin or sorbitan monooleate and type of co-surfactants - polysorbate 20 or polysorbate 80) on the physicochemical characteristics of the nanoemulsions, as well as on the skin permeation/retention of the synthetic chalcone in porcine skin. In order to evaluate the stability of the systems, the antileishmanial assay was performed against Leishmania amazonensis 24 hours and 60 days after the preparation of the nanoemulsions. The formulation composed of soybean lecithin and polysorbate 20 presented suitable physicochemical characteristics (droplet size 171.9 nm; polydispersity index 0.14; zeta potential -39.43 mV; pH 5.16; and viscosity 2.00 cP), drug content (91.09%) and the highest retention in dermis (3.03 µg·g(-1)) - the main response of interest - confirmed by confocal microscopy. This formulation also presented better stability of leishmanicidal activity in vitro against L. amazonensis amastigote forms (half maximal inhibitory concentration value 0.32±0.05 µM), which confirmed the potential of the nanoemulsion soybean lecithin and polysorbate 20 for CL treatment.
45种培养基配方 45种培养基配方 (细菌与植物培养基) 1. Acetobacter Medium (醋酸菌培养基) Glucose (葡萄糖) 100g Yeasst extract (酵母膏) 10g CaCO3 20g Agar (琼脂) 15g Distilled water (蒸馏水) 1000ml
45Ca2+ uptake study in PC12 cells
, 2mM CaCl2, 10 mM Hepes, pH 7.4) every 15 minutes for 1 hour at 37o C. 3. Add 45Ca2+ (2 µCi/ml) to Ca2+ -free buffer (secretion buffer without 2 mM CaCl2), and drugs to the labelled buffer at 37o C. 4. Incubate the cells with labelled
The Cell Environment (including types of culture medium)
" buffering system where gaseous CO2 balances with the CO3 / HCO3 content of the culture medium and (ii) chemical buffering using a zwitterion called HEPES (Prod. No. H4034). Cultures using natural bicarbonate/CO2 buffering systems need to be maintained
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