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(cè)人血清中的弗朗西斯菌/布魯氏菌 IgG/IgM抗體

產(chǎn)品規(guī)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(chóng)病、立克次體、果氏巴貝西蟲(chóng)、馬焦蟲(chóng)、牛焦蟲(chóng)、利什曼蟲(chóng)、新包蟲(chóng)、弓形蟲(chóng)、貓流感病毒、貓冠狀病毒、貓皰疹病毒、犬瘟病毒、犬細(xì)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

我司還提供其它進(jìn)口或國(guó)產(chǎn)試劑盒：登革熱、瘧疾、西尼羅河、立克次體、無(wú)形體、蜱蟲(chóng)、恙蟲(chóng)、利什曼原蟲(chóng)、RK39、漢坦病毒、深林腦炎、流感、A鏈球菌、合胞病毒、腮病毒、乙腦、寨卡、黃熱病、基孔肯雅熱、克錐蟲(chóng)病、違禁品濫用、肺炎球菌、軍團(tuán)菌、化妝品檢測(cè)、食品安全檢測(cè)等試劑盒以及日本生研細(xì)菌分型診斷血清、德國(guó)SiFin診斷血清、丹麥SSI診斷血清等產(chǎn)品。

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【公司名稱(chēng)】 廣州健侖生物科技有限公司
【】    楊永漢 
【】 
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【公司地址】 廣州清華科技園創(chuàng)新基地番禺石樓鎮(zhèn)創(chuàng)啟路63號(hào)二期2幢101-3室
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黑爾的理論文章并沒(méi)有立即引發(fā)轟動(dòng)，但因足夠有趣，他得以進(jìn)入馬克斯·普朗克生物物理化學(xué)研究所工作。在隨后的幾年中，他研制出一個(gè)STED顯微鏡，并在2000年以光學(xué)顯微鏡從未達(dá)到的分辨率獲得了大腸桿菌的圖像，用實(shí)踐證明了自己的理論。
威廉·莫納：探測(cè)單個(gè)熒光分子的*人
大多數(shù)的化學(xué)方法，例如測(cè)量熒光，科學(xué)家需要同時(shí)研究數(shù)百萬(wàn)個(gè)分子。很長(zhǎng)一段時(shí)間里，他們都在夢(mèng)想能夠測(cè)量單個(gè)分子，因?yàn)楂@得的認(rèn)知越豐富、越詳盡，理解就越深入，比如疾病是發(fā)展的。因此，1989年，當(dāng)在IBM研究中心工作的威廉·莫納成功地測(cè)量了單個(gè)分子的光吸收時(shí)，他也為單分子顯微鏡的發(fā)展奠定了基礎(chǔ)。他的實(shí)驗(yàn)啟發(fā)了許多化學(xué)家們將目光投向單個(gè)分子，其中就包括埃里克·貝齊格。
1997年，莫納進(jìn)入加州大學(xué)圣地亞哥分校，開(kāi)始了讓綠色熒光蛋白呈現(xiàn)彩虹的所有顏色的研究。他發(fā)現(xiàn)，綠色熒光蛋白的一個(gè)變體發(fā)出的熒光可被隨意地開(kāi)啟和關(guān)閉——當(dāng)受到波長(zhǎng)488納米的光激發(fā)時(shí)，蛋白開(kāi)始發(fā)出熒光，但不久就會(huì)逐漸熄滅。他將這些蛋白質(zhì)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(guī)光學(xué)顯微鏡下，可以看到單個(gè)分子的光，它們就像一盞盞帶開(kāi)關(guān)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.