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本文引用的文献

1
Use of colloidal gold particles in double-labeling immunoelectron microscopy of ultrathin frozen tissue sections.胶体金颗粒在超薄冷冻组织切片双标记免疫电子显微镜中的应用。
J Cell Biol. 1981 Jun;89(3):653-65. doi: 10.1083/jcb.89.3.653.
2
An immunocolloid method for the electron microscope.一种用于电子显微镜的免疫胶体方法。
Immunochemistry. 1971 Nov;8(11):1081-3. doi: 10.1016/0019-2791(71)90496-4.
3
Coloidal gold, ferritin and peroxidase as markers for electron microscopic double labeling lectin techniques.胶体金、铁蛋白和过氧化物酶作为电子显微镜双标记凝集素技术的标志物。
J Histochem Cytochem. 1978 Mar;26(3):163-9. doi: 10.1177/26.3.632554.
4
Location of lectin receptors on rat hepatocytes by transmission and scanning electron microscopy.通过透射电子显微镜和扫描电子显微镜观察大鼠肝细胞上凝集素受体的定位
Experientia. 1978 Feb 15;34(2):274-6. doi: 10.1007/BF01944725.
5
Ultrastructural localization of intracellular antigens by the use of protein A-gold complex.利用蛋白A-金复合物对细胞内抗原进行超微结构定位。
J Histochem Cytochem. 1978 Dec;26(12):1074-81. doi: 10.1177/26.12.366014.
6
Colloidal gold, a useful marker for transmission and scanning electron microscopy.胶体金,一种用于透射电子显微镜和扫描电子显微镜的有用标记物。
J Histochem Cytochem. 1977 Apr;25(4):295-305. doi: 10.1177/25.4.323352.
7
Adsorption of horseradish peroxidase, ovomucoid and anti-immunoglobulin to colloidal gold for the indirect detection of concanavalin A, wheat germ agglutinin and goat anti-human immunoglobulin G on cell surfaces at the electron microscopic level: a new method, theory and application.辣根过氧化物酶、卵类粘蛋白和抗免疫球蛋白吸附于胶体金上用于在电子显微镜水平间接检测细胞表面的伴刀豆球蛋白A、麦胚凝集素和山羊抗人免疫球蛋白G:一种新方法、理论及应用
J Histochem Cytochem. 1977 Nov;25(11):1187-200. doi: 10.1177/25.11.21217.

用于免疫电子显微镜的蛋白A-胶体金探针的大小测定

Sizing of protein A-colloidal gold probes for immunoelectron microscopy.

作者信息

Slot J W, Geuze H J

出版信息

J Cell Biol. 1981 Aug;90(2):533-6. doi: 10.1083/jcb.90.2.533.

DOI:10.1083/jcb.90.2.533
PMID:7026575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2111877/
Abstract

Gold particles in colloidal solutions often vary considerably in size. The finest sols (diameter less than 15 nm), especially, are very heterogeneous, as is indicated by coefficients of variance (CV) of 25-35%. We have complexed staphylococcal protein A with gold particles (PA/Au) and then fractionated the preparations by glycerol or sucrose gradient centrifugation into very homogeneous subfractions. In this way, PA/Au probes of almost any size between 4.5 and 15 nm could be prepared. The variation of the gold particles in these fractions resulted in CV's between 9 and 16%. The reactivity of the PA/Au complex was not affected by the gradient procedure, as was shown by single- and double-labeling immunocytochemistry of ultrathin cryosections of rat pancreatic tissue.

摘要

胶体溶液中的金颗粒大小常常差异很大。尤其是最细的溶胶(直径小于15纳米)非常不均一,变异系数(CV)为25%至35%就表明了这一点。我们已将葡萄球菌蛋白A与金颗粒复合(PA/Au),然后通过甘油或蔗糖梯度离心将制剂分离成非常均一的亚组分。通过这种方式,可以制备出大小在4.5至15纳米之间几乎任何尺寸的PA/Au探针。这些组分中金颗粒的变异导致CV在9%至16%之间。如对大鼠胰腺组织超薄冰冻切片进行的单标记和双标记免疫细胞化学所示,PA/Au复合物的反应性不受梯度离心过程的影响。