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Merck
CN

P8203

哌嗪-N,N′-二(2-乙磺酸)

BioXtra, ≥99% (titration)

别名:

1,4-哌嗪二乙磺酸, 哌嗪-1,4-双(2-乙磺酸), 哌嗪-N,N′-双(2-乙磺酸)

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关于此项目

经验公式（希尔记法）:
C8H18N2O6S2
化学文摘社编号:
5625-37-6
分子量:
302.37
UNSPSC Code:
12161700
NACRES:
NA.25
PubChem Substance ID:
24898917
EC Number:
227-057-6
Beilstein/REAXYS Number:
817713
MDL number:
MFCD00006159

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产品名称

哌嗪-N,N′-二(2-乙磺酸), BioXtra, ≥99% (titration)

InChI key

IHPYMWDTONKSCO-UHFFFAOYSA-N

InChI

1S/C8H18N2O6S2/c11-17(12,13)7-5-9-1-2-10(4-3-9)6-8-18(14,15)16/h1-8H2,(H,11,12,13)(H,14,15,16)

SMILES string

OS(=O)(=O)CCN1CCN(CC1)CCS(O)(=O)=O

product line

BioXtra

assay

≥99% (titration)

form

powder

impurities

Insoluble matter, passes filter test

ign. residue (900°C)

≤0.5% (as SO4)

loss

≤0.5% loss on drying, 110°C

useful pH range

6.1-7.5

pKa (25 °C)

6.8

mp

>300 °C (lit.)

solubility

1 M NaOH: 0.5 M at 20 °C, clear, colorless

anion traces

chloride (Cl-): ≤0.2%

cation traces

Al: ≤0.005%
Ba: ≤0.0005%
Bi: ≤0.0005%
Ca: ≤0.005%
Cd: ≤0.0005%
Co: ≤0.0005%
Cr: ≤0.0005%
Cu: ≤0.0005%
Fe: ≤0.0005%
K: ≤0.005%
Li: ≤0.0005%
Mg: ≤0.0005%
Mn: ≤0.0005%
Mo: ≤0.0005%
Na: ≤0.1%
Ni: ≤0.0005%
Pb: ≤0.0005%
Sr: ≤0.0005%
Zn: ≤0.0005%

absorption

≤0.1 at 260 in 1 M NaOH at 0.5 M
≤0.1 at 280 in 1 M NaOH at 0.5 M

application(s)

diagnostic assay manufacturing

Quality Level

400

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相关类别

Analysis Note

BioXtra PIPES已经过痕量元素分析。特定批次的结果见分析证书(CoA)。 BioXtra PIPES适用于需要严格控制元素含量的应用。

Application

使用PIPES用于分离琼脂糖凝胶中的乙醛酸化RNA、核酸酶S1的RNA作图以及核糖核酸酶保护检测的实验方法已被报道。PIPES已被用作戊二醛固定组织样品的缓冲液。,
PIPES已被用于蛋白结晶。， PIPES在tubulin
α和β亚基在免疫吸附凝胶上解析后进行重构的应用已被描述。PIPES已被推荐用于半胱天冬酶3、6、7和8体外研究的缓冲液中。
一项已发表的研究表明了PIPES在蛋白质分析等应用中可作为非金属离子络合缓冲液。PIPES在细胞培养中已被用于如在大肠杆菌中对热稳定突变膜蛋白进行工程化改造等应用。

General description

PIPES是乙磺酸缓冲盐系列之一，由Good等人首先开发 以满足某些标准：中值pKa，最大水溶性和在所有其他溶剂中的最小溶解度，最小盐效应，pKa随温度的变化最小，化学和酶学稳定，在可见光或紫外光谱范围的最小吸收，易于合成。由于它在37 °C的pKa接近生理pH，PIPES还可用于细胞培养工作。

Other Notes

Sigma-Aldrich公司提供生物性能认证的细胞培养用PIPES(产品编号 P1851) 以及其他几种不同的盐类，以为缓冲液制备提供便利。

Preparation Note

缓冲液制备可通过向PIPES游离酸中加入碱溶液，滴定到适当的pH值，或采用等摩尔的钠盐溶液和二钠盐溶液混合滴定到适当的pH值。

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000514185
0000514185
0000509903
0000509902
0000509903

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Y Zhou et al.
The Journal of biological chemistry, 275(10), 6975-6979 (2000-03-04)
The poor stability of membrane proteins in detergent solution is one of the main technical barriers to their structural and functional characterization. Here we describe a solution to this problem for diacylglycerol kinase (DGK), an integral membrane protein from Escherichia
Q Yu et al.
Analytical biochemistry, 253(1), 50-56 (1997-11-14)
Of the 20 well-known buffers proposed by Good, all but 3 form metal ion complexes which can result in serious interferences, particularly in protein analyses. The structural features responsible for such complex formation have been identified. Based on a mechanistic
A Giraudel et al.
Biochemistry, 37(24), 8724-8734 (1998-06-24)
The dissociation and separation of the tubulin alpha- and beta-subunits have been achieved by binding alpha-subunits to an immunoadsorbent gel and selectively inducing release of free beta-subunits. The immunoadsorbent gel was prepared by coupling the monoclonal antibody YL1/2 to Sepharose
K E Loesser et al.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 34(11), 1477-1485 (1986-11-01)
We have modified the Lowicryl K4M low-temperature dehydration and embedding procedure for immunoelectron microscopy to provide improved ultrastructural detail and facilitate the localization of actin and tubulin in isolated rat adrenocortical cells, chick spinal cord with attached dorsal root ganglia
S Haviernick et al.
Journal of microscopy, 135(Pt 1), 83-88 (1984-07-01)
It is suggested that the use of Hanks' + pipes + sucrose buffers, in combination with glutaraldehyde and osmium tetroxide fixatives, represent an excellent mode of preparation of fresh and cultured peripheral blood leucocytes, not only for transmission electron microscopy
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实验方案

Restriction Enzyme Cloning Manual Buffer Recipes

TE Buffer; Elution Buffer; 10x Ligation Buffer; 0.5 M PIPES Buffer; Inoue Transformation Buffer

Immunofluorescence Labeling of Cells

Cell staining can be divided into four steps: cell preparation, fixation, application of antibody, and evaluation.

细胞免疫荧光标记

细胞染色可分为四个步骤：细胞制备、固定、抗体孵育和评估。

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

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