相关实验视频

Updated: Jun 19, 2026

Selection of Aptamers for Amyloid β-Protein, the Causative Agent of Alzheimer's Disease
15:23

Selection of Aptamers for Amyloid β-Protein, the Causative Agent of Alzheimer's Disease

Published on: May 14, 2010

一个阿尔法球蛋白与病理突触液中的氨酸蛋白的结合

J SANDSON, D HAMERMAN

    Science (New York, N.Y.)
    |October 2, 1964
    PubMed
    概括

    研究人员使用子免疫接种在病理性突液中发现了一种独特的α球蛋白. 这种特定的蛋白质在正常液体中不存在,显示出对某些疾病的生物标志物的潜力.

    关键词:
    阿尔法环球蛋白 (ALPHA GLOBULIN) 是一种抗原 - 抗体反应实验室研究实验室研究氨酸酸是什么? 氨酸是什么?免疫电的存在在前面的测试.蛋白质是一种蛋白质.子子是什么意思血清球体蛋白质是什么综合体液体 (SYNOVIAL FLUID) 是一种液体.

    更多相关视频

    A Tailored HPLC Purification Protocol That Yields High-purity Amyloid Beta 42 and Amyloid Beta 40 Peptides, Capable of Oligomer Formation06:34

    A Tailored HPLC Purification Protocol That Yields High-purity Amyloid Beta 42 and Amyloid Beta 40 Peptides, Capable of Oligomer Formation

    Published on: March 27, 2017

    A11-positive β-amyloid Oligomer Preparation and Assessment Using Dot Blotting Analysis06:17

    A11-positive β-amyloid Oligomer Preparation and Assessment Using Dot Blotting Analysis

    Published on: May 22, 2018

    相关概念视频

    Protein Complex Assembly02:41

    Protein Complex Assembly

    Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types.  Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
    Many viruses self-assemble into a fully functional unit using the infected host cell to...
    Amyloid Fibrils03:03

    Amyloid Fibrils

    Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
    Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining, normally used to...
    Amyloid Fibrils03:03

    Amyloid Fibrils

    Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
    Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining, normally used to...