貓皰疹病毒IgG免疫熒光玻片

貓皰疹病毒IgG免疫熒光玻片

Feline Herpesvirus IgG IFA Substrate slide

廣州健侖生物科技有限公司

主要用途：用于檢測貓血清中貓皰疹病毒IgG抗體

產品規格：12 孔/張,10 張/盒

主要產品包括：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。

貓皰疹病毒IgG免疫熒光玻片

我司還提供其它進口或國產試劑盒：登革熱、瘧疾、西尼羅河、立克次體、無形體、蜱蟲、恙蟲、利什曼原蟲、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、克錐蟲病、違禁品濫用、肺炎球菌、軍團菌、化妝品檢測、食品安全檢測等試劑盒以及日本生研細菌分型診斷血清、德國SiFin診斷血清、丹麥SSI診斷血清等產品。

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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
【企業文化】

例如，細胞通過將三個甲基附著到H3組蛋白的一個特異位點上就可以關閉一些基因。而將三個甲基附著到另一個H3位點上，這種稱之為H3K4me3的修飾則可對基因表達發揮正調控效應。細胞通常將H3K4me3標記添加到基因組小段區域的組蛋白上，然而現在研究人員注意到這種標記有時可以遍布于更大的區域，修飾大量的組蛋白。
為了查明這些大H3K4me3標記區域是否在組蛋白密碼中傳送了一種信息，斯坦福大學的分子遺傳學家Anne Brunet和同事們在20多種不同的細胞類型中追蹤了它們的存在。他們發現在不同的細胞類型中廣大的H3K4me3區域標記了不同的基因。由此，研究人員認識到根據廣大H3K4me3區域的染色質定位，他們就可以將肝細胞與肌肉細胞或腎細胞區分開來。此外，他們還注意到這些H3K4me3區域往往標記的是對細胞功能至關重要，或是幫助細胞確立*身份的一些基因。例如，在胚胎干細胞中它們出現在控制細胞特化能力的一些基因上。
研究人員在成體神經祖細胞中利用rnai技術，進一步證實這些標記表明了細胞的身份。當他們利用RNAi來下調攜帶大塊H3K4me3標記的一些基因時，發現損害了細胞增殖和生成神經元的能力。而當研究人員沉默只有短H3K4me3標記區域或根本沒有H3K4me3區域的基因時，祖細胞仍然正常分裂。換句話說，大H3K4me3標記區域的存在有可能幫助了細胞終身維持身份。盡管細胞利用了幾種方法來確立它們的身份，“我們發現了一種新的標記，”Brunet說。
凱斯西儲大學表觀基因組學家Peter Scacheri對這篇論文給予了高度的評價：“我認為它將震動研究團體。盡管許多其他的科學家們一直在研究H3K4me3標記，認為這一標記可以區分所有的細胞類型這一觀點真是令人震驚。檢測這些標記非常容易，因此這一研究發現使得人們能夠快速地鑒別一些細胞類型，在諸如癌癥診斷等情況下它將派上用場。”

當你期待的東西——比如你在餐廳點餐——或者引發你興趣的東西，這時*的電節律就會席卷你的大腦。這些電波被稱為伽馬振蕩，它們反映了細胞的交響曲，即興奮性和抑制性相互協調。盡管γ波的作用一直有爭論，但其已與更高級別的腦功能相關聯，以及它的干擾模式已與精神分裂癥，阿爾茨海默氏病，自閉癥，癲癇癥和其它疾病有關。
現在，索爾克研究所的新研究表明，小有名氣的被稱為星形膠質細胞的大腦支持細胞，實際上可能是控制這些電波的主要參與者。相關文章發表于2014年7月28日的《PNAS》雜志上。
索爾克研究人員報告了新的，意想不到的策略(通過禁用星形膠質細胞而不是神經元)減小伽馬振蕩。在這個過程中，研究組表明，星形膠質細胞有助于伽馬振蕩形成，這對于某些形式的記憶是至關重要的。
“這可以被稱為一個確鑿的證據，”合作者Terrence Sejnowski說。他是索爾克生物科學研究所計算神經生物學實驗室的負責人和霍華德休斯醫學研究所的研究員。“有數百篇論文認為伽馬振蕩和記憶力以及注意力有關。這是*，我們已經能夠做一個因果的實驗。通過選擇性地阻斷伽馬振蕩，研究表明，它對大腦與世界如何相互作用有一個非常具體的影響。”
索爾克研究所的Sejnowski教授，Inder Verma和斯蒂芬·海涅曼實驗室合作， 在小鼠的大腦中，星形膠質細胞鈣信號的活動形式緊跟在伽馬振蕩之前。這表明，星形膠質細胞，和神經元一樣，使用許多相同的化學信號影響這些振蕩。

For example, cells can turn off some genes by attaching three methyls to a specific site on H3 histones. While attaching three methyls to another H3 site, this modification, called H3K4me3, can exert a positive regulatory effect on gene expression. Cells typically add the H3K4me3 marker to histones in small regions of the genome, but now researchers have noticed that such markers can sometimes modify large quantities of histones throughout a larger area.
To see if these large H3K4me3 marker regions send a message in histone codes, Anne Brunet, a molecular geneticist at Stanford University, and colleagues track their presence in more than 20 different cell types. They found that a wide range of H3K4me3 regions marked different genes in different cell types. As a result, the researchers realized that based on the chromatin localization of the vast H3K4me3 region, they could distinguish hepatocytes from muscle cells or kidney cells. In addition, they also noted that these H3K4me3 regions often tagged genes that are crucial to cellular function or help cells establish unique identities. For example, in embryonic stem cells they appear on a few genes that control the cell's specialized ability.
Using rnai technology in adult neural progenitors, the researchers further confirmed that these markers indicate cellular identity. When they used RNAi to down-regulate a few genes that carry large H3K4me3 markers, they were found to impair the ability of cells to proliferate and produce neurons. When researchers silenced only the short H3K4me3-tagged region or no H3K4me3 region, the progenitor cells normally split. In other words, the presence of a large H3K4me3 tagged region may have helped the cell stay alive for life. Although the cells utilize several ways to establish their identity, "we found a new marker," Brunet said.
Peter Scacheri, an epigenomologist at Case Western Reserve University, commented highly on the paper: "I think it will shake the research community, and while many other scientists have been studying the H3K4me3 marker, they think the marker distinguishes all Of the cell types are so alarming.The detection of these markers is so easy that the study found that it enabled people to quickly identify a few cell types that would be useful in cases such as cancer diagnosis.

When you look for something - such as when you order at a restaurant - or something that interests you, the unique rhythm rolls over your brain. These waves are called gamma oscillations, and they reflect the symphony of the cell, the excitatory and inhibitory coordination of each other. Although the role of gamma-wave has been debated, it has been associated with higher levels of brain function and its mode of interference has been associated with schizophrenia, Alzheimer's disease, autism, epilepsy and other diseases .
Now, new studies at the Salk Institute show that the little-known brain-supporting cells, called astrocytes, could actually be the main players in controlling these waves. The article was published in the July 28, 2014 PNAS magazine.
Sork researchers reported new and unexpected strategies to reduce gamma oscillations by disabling astrocytes instead of neurons. In the process, the team showed that astrocytes help form gamma oscillations, which are crucial for some forms of memory.
"This can be called a conclusive evidence," said collaborator Terrence Sejnowski. He is the head of the computational neurobiology lab at the Salk Institute for Biological Sciences and a researcher at the Howard Hughes Medical Institute. "Hundreds of papers have argued that gamma oscillations are associated with memory and attention, and for the first time, we have been able to do a causal experiment, and by selectively blocking gamma oscillations, research shows how it interacts with the world and the brain The role has a very specific impact. "
In collaboration with Professor Sejnowski at the Salk Institute, Inder Verma, and Stephen Heinemann Laboratories, the astroglial calcium signaling activity follows the gamma oscillations in the brains of mice. This suggests that astrocytes, like neurons, affect many of these oscillations using many of the same chemical signals.