AMPSO
目录号 : GC66480
AMPSO 是一种碱性转移缓冲液，可用于将强碱性蛋白质从凝胶转移到硝酸纤维素中, 而不会降低其他蛋白质的转移效率。AMPSO 可用于 Western Blot 分析、PCR 扩增以及多种其他应用。
Cas No.:68399-79-1
Sample solution is provided at 25 µL, 10mM.
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Quality Control & SDS
- View current batch:
- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
AMPSO is an alkaline transfer buffer that can be used to transfer strongly basic proteins from gels into nitrocellulose without reducing the transfer efficiency of other proteins. AMPSO can be used for Western Blot analysis, PCR amplification and many other applications[1].
[1]. B Szewczyk, et al. A method for the efficient blotting of strongly basic proteins from sodium dodecyl sulfate-polyacrylamide gels to nitrocellulose. Anal Biochem. 1985 Nov 1;150(2):403-7.
| Cas No. | 68399-79-1 | SDF | Download SDF |
| 分子式 | C7H17NO5S | 分子量 | 227.28 |
| 溶解度 | 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。 |
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| 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。 | ||
| 制备储备液 | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 4.3999 mL | 21.9993 mL | 43.9986 mL |
| 5 mM | 0.88 mL | 4.3999 mL | 8.7997 mL |
| 10 mM | 0.44 mL | 2.1999 mL | 4.3999 mL |
| 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 | 只 |
| 第二步：请输入动物体内配方组成（配方适用于不溶于水的药物；不同批次药物配方比例不同，请联系GLPBIO为您提供正确的澄清溶液配方） | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度： mg/ml；
DMSO母液配制方法： mg 药物溶于 μL DMSO溶液（母液浓度 mg/mL，
体内配方配制方法：取 μL DMSO母液，加入 μL PEG300，混匀澄清后加入μL Tween 80，混匀澄清后加入 μL saline，混匀澄清。
1. 首先保证母液是澄清的；
2.
一定要按照顺序依次将溶剂加入，进行下一步操作之前必须保证上一步操作得到的是澄清的溶液，可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
AMPSO: a new particle swarm method for nearest neighborhood classification
IEEE Trans Syst Man Cybern B Cybern 2009 Oct;39(5):1082-91.PMID:19336325DOI:10.1109/TSMCB.2008.2011816.
Nearest prototype methods can be quite successful on many pattern classification problems. In these methods, a collection of prototypes has to be found that accurately represents the input patterns. The classifier then assigns classes based on the nearest prototype in this collection. In this paper, we first use the standard particle swarm optimizer (PSO) algorithm to find those prototypes. Second, we present a new algorithm, called adaptive Michigan PSO (AMPSO) in order to reduce the dimension of the search space and provide more flexibility than the former in this application. AMPSO is based on a different approach to particle swarms as each particle in the swarm represents a single prototype in the solution. The swarm does not converge to a single solution; instead, each particle is a local classifier, and the whole swarm is taken as the solution to the problem. It uses modified PSO equations with both particle competition and cooperation and a dynamic neighborhood. As an additional feature, in AMPSO, the number of prototypes represented in the swarm is able to adapt to the problem, increasing as needed the number of prototypes and classes of the prototypes that make the solution to the problem. We compared the results of the standard PSO and AMPSO in several benchmark problems from the University of California, Irvine, data sets and find that AMPSO always found a better solution than the standard PSO. We also found that it was able to improve the results of the Nearest Neighbor classifiers, and it is also competitive with some of the algorithms most commonly used for classification.
Research on comprehensive recovery of liner schedule and container flow with hard time windows constraints
Ocean Coast Manag 2022 Jun 1;224:106171.PMID:35941892DOI:10.1016/j.ocecoaman.2022.106171.
COVID-19 has had a huge impact on the global container market. Many liner companies have adopted a blank sailing for some voyages to adjust capacity, and vessel schedule reliability continues to be sluggish. From the perspective of the container liner company, this paper studies the integrated recovery of liner schedule and container flow under the background of suspension of shipping service. With the goal of minimizing the total cost of the liner company, the hard time window constraints of the container flow on the suspended routes are set to construct the integrated recovery problem.The increased carbon emission cost during the restoration of the container flow is taken into account.A mixed integer nonlinear programming model is established, and the adaptive mutation particle swarm optimization (AMPSO) is used to solve the model. The results show that the total cost of the model is reduced by 10.66% compared with the total cost of the shipping schedule recovery model that did not consider the recovery of container flow.
High-activity biocatalysts in organic media: solid-state buffers as the immobilisation matrix for protein-coated microcrystals
Biotechnol Bioeng 2004 Jul 5;87(1):24-33.PMID:15211485DOI:10.1002/bit.20101.
Recently, we reported a new high-activity biocatalyst for use in organic media termed protein-coated microcrystals (PCMC) (Kreiner et al. [2001] Chem Commun 12:1096-1097). These novel particles consist of water-soluble micron-sized crystalline particles coated with the given biocatalyst(s) and are prepared in a one-step rapid dehydration process. In this study we extended the choice of immobilisation matrix from a simple inorganic salt, K(2)SO(4), to other compounds, both inorganic and zwitterionic, that act as solid-state buffers for biocatalysis in organic media. The catalytic activity of serine proteases subtilisin Carlsberg (SC) and alpha-chymotrypsin (CT) were significantly increased when coated onto the surface of solid-state buffers, as measured in acetonitrile/1wt% H(2)O. SC-PCMC with both organic and inorganic buffer carriers (Na-AMPSO, Na(2)CO(3), and NaHCO(3)) showed a 3-fold greater activity than that observed when using the unbuffered system (PCMC-SC/K(2)SO(4)). In comparison with freeze-dried preparations, this represents an approximately 3,000-fold increase in catalytic activity. Importantly, there is no improvement in catalytic activity upon external addition of any of the solid-state buffers to the reaction mixture. When acting in a solid-state buffer capacity, good buffering capacity was observed with SC-PCMC (3 wt% protein loading) prepared from a 1:1 mixture of AMPSO and AMPSO-Na. Alternatively, increasing the amount of solid-state buffer in the system allows improvement of the buffering. This can be achieved either by decreasing the protein loading of the SC/Na-AMPSO-PCMC or by addition of further external solid-state buffer to the reaction mixture. The catalytic activity of lipase-PCMC prepared from solid-state buffers was found less responsive to immobilisation.
Small pH gradients inhibit cytochrome c oxidase: implications for H+ entry to the binuclear center
Biochem Biophys Res Commun 1995 Nov 22;216(3):931-8.PMID:7488214DOI:10.1006/bbrc.1995.2710.
Respiring cytochrome c oxidase proteoliposomes generate internal alkalinity (delta pH) and a membrane potential (delta psi). Valinomycin collapses delta psi, increases delta pH, and slows steady state respiration. If delta pH is heterogeneously expressed trapped probes will underestimate it. Internal pH changes were therefore followed in COV containing two buffer systems of differing pKs. The alkalinization rate at pH 7 was unaffected by adding AMPSO (pK 9.0) to the usual internal HEPES (pK 7.5). At higher pH, AMPSO slowed the approach to steady state. delta pH inhibition is therefore not due to a large alkalinization in a small COV fraction. The O2-reducing center may move protons via a local aqueous phase that is near electrical and pH equilibrium with the phase inside the COV. The dielectric in this membrane region can put the center electrically 'inside' even though it is physically 'outside'.
Simultaneous detection of microorganisms in soil suspension based on PCR amplification of bacterial 16S rRNA fragments
Biotechniques 1996 Sep;21(3):463-6, 468, 470-1.PMID:8879586DOI:10.2144/96213st04.
The effect of buffer composition on simultaneous PCR amplification of 16S rRNA gene fragments of five bacterial species was examined using a number of different buffer systems. Tris-based PCR buffers at final concentrations of 10 mM proved unreliable. However, when the final concentration of Tris was increased to 75 mM, all five samples were routinely detected. The use of other buffers, 3-[(1,1-dimethyl-2-hydroxyethyl)amino]-2-hydroxypropanesulfonic acid (AMPSO) and 3-[cyclohexylamino]-2-hydroxy-1-propanesulfonic acid (CAPSO), resulted in PCR amplification of five products even at low final concentrations (10 mM). The presence of certain proteins in the amplification reaction could overcome an inhibitory effect seen when soil suspension was present in the reaction, as might occur when testing field samples for the presence of bacteria. Bovine serum albumin was found to be the most effective additive tested in overcoming inhibition.