犬細小病毒IgG免疫熒光玻片

Canine Parvovirus IgG IFA Substrate slide

廣州健侖生物科技有限公司

主要用途：用于檢測狗血清中犬細小病毒IgG抗體

產品規格：12 孔/張,10 張/盒

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犬細小病毒IgG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
【企業文化】

Sejnowski說，這個行為結果只是冰山的一角。“該識別系統是非常重要的，”他補充說，它包括認識到其他人，地點，事實，以及發生在過去的事情。有了這個新的發現，科學家們就可以開始更好地理解伽馬射線波的識別記憶的作用，他補充道。
在過去的幾年里，Whitehead研究所Susan Lindquist實驗室的研究人員一直在探究，熱休克因子1(HSF1)在支持惡性腫瘤中所起的作用。在正常細胞中，包括熱、缺氧和毒素在內的一些應激情況會激活HSF1，HSF1發揮作用維持了蛋白質穩態，幫助細胞度過艱難的時期。癌細胞能夠劫持這一熱休克反應來讓自身受益。兩年前，Lindquist實驗室證實在癌細胞中HSF1激活了與熱休克過程中正常細胞內上調的基因*不同的一組基因。
基于這一研究，該實驗室現在發現HSF1不僅對腫瘤中的癌細胞起作用，還影響了稱之為間質細胞的腫瘤微環境細胞。在這里HSF1驅動了一種轉錄程序，其不同于在鄰近癌細胞中起作用的程序。HSF1在癌細胞和間質細胞中激活，成為了一個強有力的、互補的組合推動了惡性過程。
在一系列的實驗中，Scherz-Shouval和同事們找到了確鑿的證據，證實HSF1在包括抗原抗體癌、肺癌、皮膚癌、食管癌、結腸癌和前列腺癌等各種人類腫瘤的癌相關成纖維細胞(CAFs)中激活。并且，他們發現在CAFs中HSF1激活不僅上調了一些支持惡性的基因，還抑制了周圍組織中通常觸發一種保護性、抗癌免疫反應的一些基因。盡管這樣的協同動態看似難以克服，其有可能為治療干預提供了一個真正的機會。
來自該研究另一個重要的發現是，可利用間質HSF1激活作為一種診斷和預后生物標記。分析來自抗原抗體癌患者的腫瘤樣本，科學家們發現間質中HSF1激活與患者的不良預后有關，患者的無病生存率和總生存率降低。此外，研究還發現在來自早期非小細胞肺癌患者的樣本中間質HSF1激活也與不良的預后有關。

Sejnowski said the result of this act is only the tip of the iceberg. "The identification system is very important," he added, including recognizing other people, places, facts, and what happened in the past. With this new discovery, scientists can begin to understand better the role of gamma-ray recognition memories, he added.
In the past few years, researchers at the Susan Lindquist Laboratory at the Whitehead Institute have been investigating the role of heat shock factor 1 (HSF1) in supporting malignant tumors. In normal cells, some stress conditions, including heat, hypoxia and toxins, activate HSF1, which acts to maintain protein homeostasis and help cells to pass tough times. Cancer cells can hijack this heat shock response to benefit themselves. Two years ago Lindquist Laboratories confirmed that HSF1 in cancer cells activates a compley different set of genes that are up-regulated in normal cells during heat shock.
Based on this study, the laboratory now found that HSF1 not only affects cancer cells in tumors but also affects tumor microenvironmental cells called stromal cells. Here HSF1 drives a transcription program that is distinct from the programs that play a role in neighboring cancer cells. HSF1 is activated in cancer cells and interstitial cells, becoming a powerful, complementary combination that drives the malignant process.
In a series of experiments, Scherz-Shouval and colleagues found conclusive evidence confirming that HSF1 is involved in the development of cancer-associated fibroblasts in a variety of human tumors including antigen-antibody, lung, skin, esophagus, colon and prostate Cells (CAFs) are activated. And, they found that HSF1 activation in CAFs not only up-regulates some of the genes that support malignancy, but also suppresses some of the genes in surrounding tissues that normally trigger a protective, anti-cancer immune response. While such synergistic dynamics may seem insurmountable, they may offer a real opportunity for therapeutic intervention.
Another important finding from this study is that stromal HSF1 activation can be exploited as a diagnostic and prognostic biomarker. Analyzing tumor samples from patients with antigen-antibody cancers, scientists found that HSF1 activation in the stroma was associated with poor prognosis in patients with a reduction in disease-free survival and overall survival. In addition, the study also found that stromal HSF1 activation in samples from patients with early non-small cell lung cancer is also associated with poor prognosis.