组织微阵列
心力衰竭
免疫组织化学
多克隆抗体
免疫印迹
生物
微阵列
计算生物学
癌症研究
分子生物学
抗体
基因表达
内科学
免疫学
医学
基因
遗传学
作者
Sean Lal,Lisa Nguyen,Rhenan Tezone,Fredrik Pontén,Jacob Odeberg,Amy Li,Cristobal G. dos Remedios
出处
期刊:Proteomics
[Wiley]
日期:2016-07-01
卷期号:16 (17): 2319-2326
被引量:13
标识
DOI:10.1002/pmic.201600135
摘要
Tissue MicroArrays (TMAs) are a versatile tool for high-throughput protein screening, allowing qualitative analysis of a large number of samples on a single slide. We have developed a customizable TMA system that uniquely utilizes cryopreserved human cardiac samples from both heart failure and donor patients to produce formalin-fixed paraffin-embedded sections. Confirmatory upstream or downstream molecular studies can then be performed on the same (biobanked) cryopreserved tissue. In a pilot study, we applied our TMAs to screen for the expression of four-and-a-half LIM-domain 2 (FHL2), a member of the four-and-a-half LIM family. This protein has been implicated in the pathogenesis of heart failure in a variety of animal models. While FHL2 is abundant in the heart, not much is known about its expression in human heart failure. For this purpose, we generated an affinity-purified rabbit polyclonal anti-human FHL2 antibody. Our TMAs allowed high-throughput profiling of FHL2 protein using qualitative and semiquantitative immunohistochemistry that proved complementary to Western blot analysis. We demonstrated a significant relative reduction in FHL2 protein expression across different forms of human heart failure.
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