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上海恒遠(yuǎn)生物科技有限公司>技術(shù)文章>恒遠(yuǎn)產(chǎn)品技術(shù)文獻(xiàn):抗體山羊抗兔引用文獻(xiàn)

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恒遠(yuǎn)產(chǎn)品技術(shù)文獻(xiàn):抗體山羊抗兔引用文獻(xiàn)

閱讀:704          發(fā)布時(shí)間:2020-12-30

【文獻(xiàn)標(biāo)題】Exosomal miR-9-5p secreted by bone marrow–derived mesenchymal stem cells alleviates osteoarthritis by inhibiting syndecan-1

【作者】Zhe Jin,Jiaan Ren,Shanlun Qi,et.al

【作者單位】中國醫(yī)科大學(xué)附屬第YI醫(yī)院(First Hospital of China Medical University)

【文獻(xiàn)中引用產(chǎn)品】

抗體山羊抗兔

【關(guān)鍵詞】Osteoarthritis,Bone marrow–derived mesenchymal stem cells,Exosome,microRNA-9-5p,Syndecan-1

【DOI】doi.org/10.1007/s00441-020-03193-x

【影響因子(IF)】3.11

出版期刊】《Cell and Tissue Research》

【產(chǎn)品原文引用】

Immunohistochemistry

The articular cartilage tissues were fixed in 4% paraformaldehyde for 24 h. Then, the tissues were dehydrated with gradient ethanol, paraffin-embedded and sliced into 5-μm sections. After being dewaxed, the tissue sections were dehydrated by gradient ethanol, immersed in 3% H2O2 for 10 min, followed by high-pressure antigen retrieval for 90 s. Afterwards, the sections were blocked with 100 μL 5% bovine serum albumin (BSA) solution at 37 °C for 30 min. The sections were then incubated with 100 μL rabbit anti SDC1 (1:500, ab128936, Abcam,Cambridge, MA, USA) overnight at 4 °C. The next day,the sections were incubated with biotin-labeled secondary antibody goat anti-rabbit (HY90046, Shanghai Hengyuan Biotechnology Co., Ltd., Shanghai, China) at 37 °C for 30 min. Then, the sections were incubated with streptavidin-peroxidase (Beijing Zhongshan Biotechnology Co., Ltd., Beijing, China) at 37 °C for 30 min and colored by diaminobenzidine (DAB) (Bioss Biotech, Beijing, China) at room temperature. Finally, the sections were counterstained by hematoxylin for 5 min,differentiated by 1% hydrochloric acid alcohol for 4 s and blued under running water for 20 min. The SDC1 positive cells were analyzed using Image-Pro Plus image analysis software (Media Cybernetics, Silver Springs,MD, USA). The brownish-yellow colored cells were considered as positive cells (Kelkar et al. 2017). Five highpower fields (× 200) were randomly selected from each section, with 100 cells counted in each field. The percentage of positive cells = the number of positive cells/the number of total cells and the percentage of positive cells > 10% was regarded as positive (+), < 10% as negative (−).The experiment was repeated three times independently.

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