Pluronic™ F-127(溶于 DMSO 的 20% 溶液)
Pluronic™ F-127(溶于 DMSO 的 20% 溶液)
Invitrogen™

Pluronic™ F-127(溶于 DMSO 的 20% 溶液)

溶于 DMSO* 的 Pluronic F-127 *20% 溶液是一种非离子、表面活性剂多元醇(分子量约为 12,500了解更多信息
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细胞成像入门礼
999元任选3件,1899任选6件, MitoTracker、MitoSOX等爆款应有尽有!更多
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货号数量
P3000MPPromo Image1 mL
货号 P3000MP
价格(CNY)
835.00
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Ends: 31-Dec-2025
1,123.00
共减 288.00 (26%)
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空运受限产品: 发货后, 北上广深及省会城市通常为 2-4天,二线城市 通常3-5天,三线以及偏远地区通常 6-10天,周末以及节假日顺延。
现货中心: 此类产品将由您身边的现货中心极速配送。
价格(CNY)
835.00
飞享价
Ends: 31-Dec-2025
1,123.00
共减 288.00 (26%)
Each
添加至购物车
溶于 DMSO* 的 Pluronic F-127 *20% 溶液是一种非离子、表面活性剂多元醇(分子量约为 12,500 道尔顿),已发现其有利于促进非水溶性染料和其他材料在生理培养基中的溶解。Pluronic F-127 常用于帮助分散我们离子指示剂以及我们细胞示踪剂染料(如 CFDA-SE)中的乙酰氧基甲基 (AM) 酯。

了解更多有关离子指示剂(包括钙、钾、pH 值和膜电位指示剂)的信息›

仅供科研使用。不可用于诊断程序。
规格
物理形态液体
建议的储存条件在室温下储存。
数量1 mL
Unit SizeEach

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证书

批号Certificate TypeDateCatalog Number(s)
2935433Certificate of Analysis2024年8月19日P3000MP
2714438Certificate of Analysis2023年8月16日P3000MP
2510678Certificate of Analysis2022年8月03日P3000MP
2339925Certificate of Analysis2021年8月16日P3000MP
2291566Certificate of Analysis2020年12月30日P3000MP
显示 5 条结果, 在上面搜索特定证书

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常见问题解答 (FAQ)

培养用于转染的细胞应保持起始细胞活力在90%以上。转染后,细胞活力会在3-6天后缓慢降至90%到80%区间,7天乃至更长时间后发生更显著的下降。这是使用我们推荐的实验方案时的情况,该方案不推荐在转染后对培养基进行换液或补充。

我们建议用户对一些参数进行检查,以确保获得高细胞活力:pH在7.0左右,无可见的细胞团块,CO2水平在7–8%左右(需对该值进行调节以达到适当的pH值),培养体积应为培养瓶标称容积的40%或以下,培养箱温度为37°C。如果您的培养箱中配有振荡平台,则振荡台产生的热量可能足以升高培养箱温度。我们推荐在振荡台上贴一个温度计。如果怀疑培养物的氧气供应不够充分,则使用带挡板的培养瓶可能会有帮助。光照也可能会造成某些培养基成份的降解,我们建议妥善处理和保存培养基。如果您正在使用FreeStyle 293表达培养基,则无需添加Pluronic试剂。

注意:细胞聚团的两个主要原因为:1)细胞培养密度过大,和/或2)振荡不充分。因此,充分的搅拌,按照细胞传代时间表规律的传代,并以推荐的密度培养细胞就能够防止细胞聚团。如果发现细胞聚团情况,我们则建议放弃培养物,另取一管新的冻存细胞重新开始培养。用户可能需要在一段时间内每次传代时对细胞剧烈涡旋10-30秒,直至大部分细胞都以单个的形式存在。此外,用户可于每次传代时通过沉降的方式来清除聚团细胞。用户可增加摇床的转速,并确保每次在细胞不超过1.5–2 x 106个细胞/毫升的密度时进行传代。只要细胞活力保持在95%以上时,可增加摇床的转速。在细胞转染后的至少初始2-4小时降低转速,以确保DNA-转染试剂复合物能够良好贴附和进入细胞内。用户也可在最初两次传代时以1:1000(1:200最高)的稀释比例添加抗结团试剂(货号 0010057AE),之后在转染前在不含抗结团试剂的条件下进行传代。请勿在转染过程中的任何时间点添加抗结团试剂,因为该试剂会对转染过程造成干扰。不过,转染数小时之后即可加入抗结团试剂。

Culture viability should be in the high 90% range for the seed stock that you are maintaining and growing for the transfections. After transfection, the viability will slowly decrease to the lower 90% to 80% range by about 3-6 days post-transfection and can drop more dramatically at 7 days or longer. This is when using our recommended protocol, which does not suggest any media changes or supplementation post-transfection.

A few parameters we recommend checking to assure high culture viability are: pH at ˜7.0, no visible clumping of the cells, CO2 levels at approximately 7-8% (this should be adjusted to achieve the appropriate pH), volume of culture at 40% or less of nominal flask capacity, and incubator temperature at 37 degrees C. If you have a shaker platform setup in your incubator, the platform may generate sufficient heat to increase the temperature of the incubator. We recommend using a thermometer attached to the shaker platform. Use of baffled flasks may help, if insufficient oxygenation of the cultures is suspected. We also recommend handling and storing the culture media properly, as light exposure can result in breakdown of certain media components. If you are using FreeStyle 293 Expression Medium, supplementing with Pluronic reagent is not necessary.

Find additional tips, troubleshooting help, and resources within our Protein Expression Support Center.

引用和文献 (145)

引用和文献
Abstract
Rescue of vasopressin V2 receptor mutants by chemical chaperones: specificity and mechanism.
Authors:Robben JH,Sze M,Knoers NV,Deen PM
Journal:Molecular biology of the cell
PubMed ID:16267275
Because missense mutations in genetic diseases of membrane proteins often result in endoplasmic reticulum (ER) retention of functional proteins, drug-induced rescue of their cell surface expression and understanding the underlying mechanism are of clinical value. To study this, we tested chemical chaperones and sarco(endo)plasmic reticulum Ca(2+) ATPase pump inhibitors on ... More
Indo-1 binding to protein in permeabilized ventricular myocytes alters its spectral and Ca binding properties.
Authors:Hove-Madsen L, Bers DM
Journal:Biophys J
PubMed ID:1420876
We have examined the binding of the fluorescent Ca indicator indo-1 to cellular protein in permeabilized ventricular myocytes and also to soluble and particulate myocyte protein. Using either a filtration technique or equilibrium dialysis, and conditions similar to those in a cardiac myocyte patch clamped with 100 microM indo-1 in ... More
Long-term regulation of neuronal calcium currents by prolonged changes of membrane potential.
Authors:Franklin JL, Fickbohm DJ, Willard AL
Journal:J Neurosci
PubMed ID:1315850
'Although rapid-onset, short-term regulation of neuronal Ca currents by neurotransmitters and second messengers is well documented, little is known about conditions that can cause longer-lasting changes in Ca channel function. We report here that persistent depolarization is accompanied by slowly developing long-term reduction of neuronal Ca currents. Rat myenteric neurons ... More
Regulation of cytosolic free calcium concentration by intrasynaptic mitochondria.
Authors:Martínez-Serrano A, Satrústegui J
Journal:Mol Biol Cell
PubMed ID:1550964
'By the use of digitonin permeabilized presynaptic nerve terminals (synaptosomes), we have found that intrasynaptic mitochondria, when studied "in situ," i.e., surrounded by their cytosolic environment, are able to buffer calcium in a range of calcium concentrations close to those usually present in the cytosol of resting synaptosomes. Adenine nucleotides ... More
Intracellular astrocyte calcium waves in situ increase the frequency of spontaneous AMPA receptor currents in CA1 pyramidal neurons.
Authors:Fiacco TA, McCarthy KD
Journal:J Neurosci
PubMed ID:14736858
'Spontaneous neurotransmitter release and activation of group I metabotropic glutamate receptors (mGluRs) each play a role in the plasticity of neuronal synapses. Astrocytes may contribute to short- and long-term synaptic changes by signaling to neurons via these processes. Spontaneous whole-cell AMPA receptor (AMPAR) currents were recorded in CA1 pyramidal cells ... More
145 total citations

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