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经验公式(希尔记法):
C8H18N2O6S2
化学文摘社编号:
分子量:
302.37
UNSPSC Code:
12161700
NACRES:
NA.25
PubChem Substance ID:
EC Number:
227-057-6
Beilstein/REAXYS Number:
817713
MDL number:
产品名称
哌嗪-N,N′-二(2-乙磺酸), ≥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
assay
≥99% (titration)
form
crystalline powder
useful pH range
6.1-7.5
pKa (25 °C)
6.8
mp
>300 °C (lit.)
solubility
1 M NaOH: 20 + 80 mL g, clear, colorless
application(s)
diagnostic assay manufacturing
Quality Level
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Application
戊二醛固定动植物组织标本可引起脂质丢失,引起明显的形态学改变。当采用PIPES来缓冲戊二醛固定剂时,脂质的损失和伪影被最小化。,
当超细胞化学固定采用甲次砷酸盐-缓冲戊二醛时,碱性磷酸酶活性可选择性地从某些大鼠肝细胞细胞器丢失。当使用PIPES作为缓冲液时,活性的保留率要高于60%。
当在PIPE缓冲液采用戊二醛和甲醛配伍用作固定剂时,真菌孢子固片的荧光显微镜和电镜观察是最优的。
当超细胞化学固定采用甲次砷酸盐-缓冲戊二醛时,碱性磷酸酶活性可选择性地从某些大鼠肝细胞细胞器丢失。当使用PIPES作为缓冲液时,活性的保留率要高于60%。
当在PIPE缓冲液采用戊二醛和甲醛配伍用作固定剂时,真菌孢子固片的荧光显微镜和电镜观察是最优的。
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。由于其在37℃的pKa接近生理pH,PIPES可应用于细胞培养工作。
Other Notes
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
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Use of PIPES buffer in the fixation of plant cells for electron microscopy
Salema, R. and Brandao, I.
Journal of Submicroscopic Cytology, 9, 79-79 (1973)
A R Hardham
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 33(2), 110-118 (1985-02-01)
The study of the surface properties of zoospores and cysts of the fungus Phytophthora cinnamomi required a fixation regime that would preserve the cells adequately and not interfere with binding and detection of probes on the cell surface. When they
K Yamamoto et al.
Histochemistry, 77(3), 339-351 (1983-01-01)
Effects of NaOH-PIPES buffer used as a vehicle for aldehyde fixative on alkaline phosphatase (ALPase) activity demonstrated cyto- and biochemically were compared with those of routinely used cacodylate buffer. The reaction products showing ALPase activity demonstrated ultracytochemically were confined to
The role of the buffer in the fixation of biological specimens for transmission and scanning electron microscopy
Schiff, R.I. and Gennaro, J.F., Jr.
Scanning, 2, 135-135 (1979)
Buffers for enzymes.
J S Blanchard
Methods in enzymology, 104, 404-414 (1984-01-01)
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