SIGMA E5391-250G EDTA四钠盐 194491-31-1
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SIGMA E5391-250G EDTA四钠盐 19449

1-31-1
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  • ¥196
  • Sigma-Aldrich
  • E5391-250G
  • 进口
  • 2025年07月12日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 库存

      有现货

    • 英文名

      Ethylenediaminetetraacetic acid tetrasodium salt hydrate

    • CAS号

      194491-31-1

    • 保质期

      根据瓶身LOT号查询

    • 供应商

      浙江羽翔生物科技有限公司

    • 保存条件

      常温

    • 规格

      250G

    属性

    生物来源

    synthetic (organic)

    质量水平

    200

    方案

    ≥99.0%

    表单

    powder

    技术

    ligand binding assay: suitable

    杂质

    Insoluble matter, passes filter test

    pH值(酸碱度)

    11.0-12.0 (0.1 M in H2O)

    溶解性

    H2O: 0.1 M, clear, colorless

    痕量阴离子

    chloride (Cl-): ≤0.05%
    sulfate (SO42-): ≤0.01%

    痕量阳离子

    Al: ≤0.001%
    As: ≤0.0001%
    Ba: ≤0.0005%
    Bi: ≤0.0005%
    Ca: <0.001%
    Cd: ≤0.0005%
    Co: ≤0.0005%
    Cr: ≤0.0005%
    Cu: ≤0.0005%
    Fe: ≤0.0005%
    Li: ≤0.0005%
    Mg: ≤0.0005%
    Mn: ≤0.0005%
    Mo: ≤0.0005%
    Ni: ≤0.0005%
    Pb: ≤0.0005%
    Sr: ≤0.0005%
    Zn: ≤0.0005%

    吸附

    ≤0.06 at 280 in H2O at 0.1 M
    ≤1.5 at 260 in H2O at 0.1 M

    应用

    sample preparation

    储存温度

    room temp

    SMILES字符串

    O.[Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CCN(CC([O-])=O)CC([O-])=O)CC([O-])=O

    InChI

    1S/C10H16N2O8.4Na.H2O/c13-7(14)3-11(4-8(15)16)1-2-12(5-9(17)18)6-10(19)20;;;;;/h1-6H2,(H,13,14)(H,15,16)(H,17,18)(H,19,20);;;;;1H2/q;4*+1;/p-4

    InChI key

    GXFFSKMBMYHTAE-UHFFFAOYSA-J

    应用

    EDTA 为金属蛋白酶抑制剂,有效浓度为 1-10 mM。EDTA 可用作金属蛋白酶活性中心锌离子的螯合剂,并且还可抑制其他依赖金属离子的蛋白酶,例如依赖钙的半胱氨酸蛋白酶。作为抗凝血剂时,通常使用 EDTA 的二钠或三钾盐。最佳浓度为每 mL 血液 1.5mg。
    用于消除痕量重金属对酶的抑制作用,并抑制需要二价阳离子作为辅助因子的酶。

    制备说明

    室温下溶于水的最大浓度可达 1.45M。该溶液的 pH 值约为 10 至 11,而且粘度较大。

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    图标文献和实验
    该产品被引用文献

    Comparative Anatomy of the Mammalian Corneal Subbasal Nerve Plexus.

    Investigative ophthalmology & visual science (2019-12-04)
    Carl Marfurt, Miracle C Anokwute, Kaleigh Fetcko, Erin Mahony-Perez, Hassan Farooq, Emily Ross, Maraya M Baumanis, Rachel L Weinberg, Megan E McCarron, Joseph L Mankowski
    PMID31790560
    摘要

    The subbasal nerve plexus (SNP) is the densest and most recognizable component of the mammalian corneal innervation; however, the anatomical configuration of the SNP in most animal models remains incompletely described. The purpose of the current study is to describe in detail the SNP architecture in eight different mammals, including several popular animal models used in cornea research. Corneal nerves in mouse, rat, guinea pig, rabbit, dog, macaque, domestic pig, and cow eyes were stained immunohistochemically with antiserum directed against neurotubulin. SNP architecture was documented by digital photomicrography and large-scale reconstructions, that is, corneal nerve maps, using a drawing tube attached to a light microscope. Subbasal nerve fibers (SNFs) in mice, rats, guinea pigs, dogs, and macaques radiated centrally from the corneoscleral limbus toward the corneal apex in a whorl-like or spiraling pattern. SNFs in rabbit and bovine corneas swept horizontally across the ocular surface in a temporal-to-nasal direction and converged on the inferonasal limbus without forming a spiral. SNFs in the pig cornea radiated centrifugally in all directions, like a starburst, from a focal point located equidistant between the corneal apex and the superior pole. The results of the present study have demonstrated for the first time substantial interspecies differences in the architectural organization of the mammalian SNP. The physiological significance of these different patterns and the mechanisms that regulate SNP pattern formation in the mammalian cornea remain incompletely understood and warrant additional investigation.

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    SIGMA E5391-250G EDTA四钠盐 194491-31-1
    ¥196