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弗朗西斯/布魯氏菌免疫熒光玻片
Francisella/Brucella MIF Substrate Slide
廣州健侖生物科技有限公司
主要用途:用于檢測人血清中的弗朗西斯菌/布魯氏菌 IgG/IgM抗體
產品規格:12 孔/張,10 張/盒
包括包柔氏螺旋體菌、布魯氏菌、貝納特氏立克次體、土倫桿菌、鉤端螺旋體、新型立克次體、恙蟲病、立克次體、果氏巴貝西蟲、馬焦蟲、牛焦蟲、利什曼蟲、新包蟲、弓形蟲、貓流感病毒、貓冠狀病毒、貓皰疹病毒、犬瘟病毒、犬細小病毒等病原微生物的 IFA、MIF、ELISA試劑。
弗朗西斯/布魯氏菌免疫熒光玻片
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【公司名稱】 廣州健侖生物科技有限公司
【】 楊永漢
【】
【騰訊 】 2042552662
【公司地址】 廣州清華科技園創新基地番禺石樓鎮創啟路63號二期2幢101-3室
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黑爾的理論文章并沒有立即引發轟動,但因足夠有趣,他得以進入馬克斯·普朗克生物物理化學研究所工作。在隨后的幾年中,他研制出一個STED顯微鏡,并在2000年以光學顯微鏡從未達到的分辨率獲得了大腸桿菌的圖像,用實踐證明了自己的理論。
威廉·莫納:探測單個熒光分子的*人
大多數的化學方法,例如測量熒光,科學家需要同時研究數百萬個分子。很長一段時間里,他們都在夢想能夠測量單個分子,因為獲得的認知越豐富、越詳盡,理解就越深入,比如疾病是發展的。因此,1989年,當在IBM研究中心工作的威廉·莫納成功地測量了單個分子的光吸收時,他也為單分子顯微鏡的發展奠定了基礎。他的實驗啟發了許多化學家們將目光投向單個分子,其中就包括埃里克·貝齊格。
1997年,莫納進入加州大學圣地亞哥分校,開始了讓綠色熒光蛋白呈現彩虹的所有顏色的研究。他發現,綠色熒光蛋白的一個變體發出的熒光可被隨意地開啟和關閉——當受到波長488納米的光激發時,蛋白開始發出熒光,但不久就會逐漸熄滅。他將這些蛋白質分散到凝膠中,并讓它們之間的距離大于0.2微米的阿貝衍射極限。在常規光學顯微鏡下,可以看到單個分子的光,它們就像一盞盞帶開關的小燈。
Hare's theoretical essay did not immediay provoke a sensation, but because of enough interest, he was able to enter the Max Planck Institute for Biophysical and Chemical work. In subsequent years, he developed a STED microscope and obtained the image of Escherichia coli at an unprecedented resolution with a light microscope in 2000, which proved his own theory.
William Mona: The first person to probe a single fluorescent molecule
Most chemical methods, such as measuring fluorescence, require scientists to study millions of molecules simultaneously. For a long time, they all dreamed of being able to measure a single molecule because the more cognitive and acquired, the more detailed the understanding, the more in-depth understanding, such as the development of the disease. So, when William Mona, working at the IBM Research Center, successfully measured the light absorption of a single molecule in 1989, he laid the groundwork for the development of single-molecule microscopy. His experiments inspired many chemists to turn their attention to individual molecules, including Eric Bezig.
In 1997, Mona entered the University of California, San Diego, and began researching all the colors that make GFP rainbow. He found that the fluorescence emitted by a variant of a green fluorescent protein could be turned on and off as desired - the protein started to fluoresce when excited by light at a wavelength of 488 nm, but soon extinguished. He spreads these proteins into the gel with a distance between them greater than the Abbe diffraction limit of 0.2 microns. Under a regular light microscope, you can see a single molecule of light that resembles a small light with a switch.