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1
2019 - 03 - 08
1 月 28 日,國際學(xué)術(shù)期刊 Circulation Research 在線發(fā)表了中國科學(xué)院上海營養(yǎng)與健康研究所宗耕課題組與哈佛大學(xué)公共衛(wèi)生學(xué)院營養(yǎng)系合作的最新研究成果 “Associations of Monounsaturated Fatty Acids from Plant and Animal Sources with Total and Cause-Specific Mortality in Two US Prospective Cohort Studies”。該研究發(fā)現(xiàn)較高的植物來源單不飽和脂肪酸(MUFA-Ps)攝入量與較低的總死亡率相關(guān),而動(dòng)物來源單不飽和脂肪酸(MUFA-As)的攝入則與較高死亡率相關(guān)。另外,用植物來源單不飽和脂肪酸替代飽和脂肪酸(SFAs)、精加工的碳水化合物或反式脂肪可以顯著降低死亡風(fēng)險(xiǎn)。在全球范圍內(nèi),心血管疾?。–VD)和癌癥是造成過早死亡的最主要原因。目前,越來越多的研究表明采取健康的生活方式(如戒煙、增加體力活動(dòng)和提高膳食質(zhì)量等)能夠有效降低過早死亡的風(fēng)險(xiǎn)。多個(gè)國家的膳食指南均強(qiáng)調(diào)了膳食脂肪的質(zhì)量對(duì)預(yù)防慢性疾病的重要性,尤其提倡植物油及其他植物來源的脂肪攝入。例如,膳食中的多不飽和脂肪酸(PUFAs)主要來自植物,而現(xiàn)有的研究表明 PUFAs 能夠降低心血管疾病風(fēng)險(xiǎn)和死亡率的關(guān)系。與之相比,飲食中的單不飽和脂肪酸只有一半來自植物油(尤其...
2
2019 - 07 - 05
據(jù)新華社電 美國疾病控制和預(yù)防中心研究團(tuán)隊(duì)發(fā)現(xiàn),正在剛果(金)使用的兩種試驗(yàn)性療法對(duì)抗擊當(dāng)前的埃博拉疫情有效。7 月 9 日發(fā)表在英國《柳葉刀—傳染病》雜志上的研究顯示,在實(shí)驗(yàn)室中,抗病毒藥物 Remdesivir,以及由三種抗體組成的抗埃博拉藥物 ZMapp 可阻斷新一輪埃博拉疫情的致病毒株在人類細(xì)胞中增長。確認(rèn)抗病毒藥物有效的關(guān)鍵之一在于找到此次疫情的致病毒株。論文第一作者、美疾控中心微生物學(xué)家勞拉 · 麥克馬倫說,目前在剛果(金)試用的療法均針對(duì)以前疫情中獲取的埃博拉毒株,而埃博拉是一種核糖核酸(RNA)病毒,會(huì)不斷變異,因此確定現(xiàn)有療法是否對(duì)新毒株奏效至關(guān)重要。美疾控中心研究人員沒有當(dāng)前在剛果(金)傳播的 “伊圖里” 毒株樣本,但他們從開源基因庫中獲得病毒序列數(shù)據(jù),使用 “反向遺傳學(xué)” 技術(shù)重組了毒株。這項(xiàng)技術(shù)有助于研究人員更多了解新毒株在埃博拉家族樹中的位置,從而尋找更多潛在療法,并測(cè)試各類新療法的有效性,還可與未來的新毒株進(jìn)行比對(duì)。研究中還發(fā)現(xiàn),2014 年到 2016 年西非多國爆發(fā)埃博拉疫情期間開發(fā)的一種實(shí)驗(yàn)室病毒診斷方法可用于診斷 “伊圖里” 毒株。(周舟)文章摘自:生物360
3
2020 - 02 - 21
2020年2月16日訊 /生物谷BIOON /--國家指南建議前列腺癌患者多吃蔬菜,這可能會(huì)減少癌癥的進(jìn)展和死亡。但在一項(xiàng)III期隨機(jī)臨床試驗(yàn)中,前列腺癌患者被指定每天吃7份或更多的蔬菜和水果,卻沒有發(fā)現(xiàn)額外的微量營養(yǎng)元素?cái)z入的保護(hù)作用。'這些數(shù)據(jù)表明,盡管科學(xué)和公眾輿論普遍認(rèn)為需要吃蔬菜,但多吃蔬菜缺確實(shí)不會(huì)改變前列腺癌的病程。據(jù)我們所知,它不會(huì)抑制或治愈它。然而,雖然多吃水果和蔬菜的健康飲食和多做運(yùn)動(dòng)不一定能治愈癌癥,但它可能使身體更強(qiáng)壯、更健康,這可能有助于患者忍受癌癥治療。'圖片來源:Wikipedia這項(xiàng)研究近日發(fā)表在《Journal of the American Medical Association》上,,由加州大學(xué)圣地亞哥分校Moores癌癥中心和Roswell Park綜合癌癥中心的研究人員完成,招收了478名年齡在50到80歲男性。這些患者被診斷為早期前列腺腺癌,并參與了一個(gè)積極的監(jiān)測(cè)項(xiàng)目,在該項(xiàng)目中,患者推遲立即治療,直到病情惡化?;颊弑浑S機(jī)分為兩組,一組接受關(guān)于飲食和前列腺癌的書面信息,另一組接受電話咨詢的行為干預(yù)項(xiàng)目,該項(xiàng)目鼓勵(lì)參與者食用類胡蘿卜素含量高的食物,如綠葉蔬菜、胡蘿卜和西紅柿,以及十字花科蔬菜,如西蘭花和卷心菜。兩組都接受了兩年的監(jiān)測(cè)。被分配到干預(yù)組的患者增加了水果和蔬菜的攝入量,達(dá)到了有統(tǒng)計(jì)學(xué)意義的程度,明顯多于對(duì)照組患者。...
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產(chǎn)品名稱:

Premo? FUCCI Cell Cycle Sensor (BacMam 2.0)

上市日期: 2019-04-18
產(chǎn)品類別: INVITROGEN

規(guī)格

Color:Green,?Red-Orange
Delivery Method:Baculovirus (BacMam System)
Detection Method:Fluorescent
Emission Class:Visible
Excitation Class:Visible
Excitation?Emission (nm):488?510 (Green),?555?584 (Red)
For Use With (Equipment):Flow Cytometer,?Fluorescence Microscope,?Fluorescent Imager,?High Content Instrument,?Tali? Image-Based Cytometer
Form:Liquid
Label or Dye:GFP (EmGFP),?RFP (TagRFP)
Product Line:Premo?
Product Size:2 x 200 μL
Quantity:2 vials (200 μl each)
Sub-Cellular Localization:Nucleus
Technique:Fluorescence Intensity
Shipping Condition:Wet Ice


  • 產(chǎn)品描述
  • 產(chǎn)品功能
  • 產(chǎn)品參數(shù)

描述

Premo? FUCCI Cell Cycle Sensor is a fluorescent, two-color sensor of cell cycle progression and division in live cells. It allows accurate and sensitive cell cycle analysis of individual cells or a population of cells by fluorescence microscopy, flow cytometry, or high-content imaging.

At 2 x 200 μL, this is a smaller pack size version (1/5 volume) of the popular full-size product and perfect for testing its performance in your system.

The Premo? FUCCI Cell Cycle Sensor is delivered by highly efficient BacMam 2.0 technology, enabling cell cycle studies in essentially any cell type. Provided in a ready-to-use format—simply add, incubate, and image. Premo? FUCCI affords highly efficient transient expression in cell lines, primary cells, and stem cells.

Premo? FUCCI Cell Cycle Sensor is:

? Accurate: Cell-cycle controlled expression of bright GFP and RFP indicators for live cell analysis of individual cells or populations
? Highly Efficient: >90% transduction of a wide range of mammalian cell lines, including primary cells, stem cells, and neurons
? Fast and Convenient: Simply add Premo? FUCCI Cell Cycle Sensor to your cells in complete medium, incubate overnight, and analyze
? Safe: BacMam reagents are non-integrating and non-replicating in mammalian cells, lack observable cytopathic effects, and are suitable for biosafety level (BSL) 1 handling

Study Cell Cycle in the Relevant Cellular Context
If you are studying cell cycle regulators, cell differentiation, or are developing anti-cancer compounds against cell cycle-related targets, Premo? FUCCI is a superbly sensitive and accurate sensor tool. The efficient transduction and transient expression allows you to conduct these experiments in the biologically relevant cell types.

Simple, Quick Cell Cycle Visualization
Simply add the ready-to-use Premo? FUCCI cell cycle sensor to your cells in complete medium, incubate overnight, then visualize cell cycle progression in populations of cells using fluorescence microscopy, flow cytometry, or high content imaging instruments. Cells change from red in the G1 to yellow in the G1/S interphase and green in S, G2, and M phases, as fusions of emGFP and TagRFP coupled to two cell cycle-regulated proteins are expressed and degraded.

How It Works
Premo? FUCCI is derived from the fluorescence ubiquitination cell cycle indicator (FUCCI), developed by Miyawaki and colleagues (Ref 1). FUCCI is based on two cell cycle-regulated proteins, geminin and Cdt1, fused to one green (emGFP) and red (TagRFP) fluorescent protein, respectively. As Cdt1 and geminin are present only during specific phases of the cell cycle, the fluorescent protein partner is similarly cell-cycle dependent. Ubiquitination by specific ubiquitin E3 ligases target the fusion constructs in the proteasome for degradation. E3 ligases display temporal regulation of activity, resulting in biphasic cycling of geminin and Cdt1 levels during the cell cycle. Geminin-GFP is degraded in the G1 phase; the presence of Cdt1-TagRFP is indicated by red fluorescence within nuclei. During the S, G2, and M phases, however, Cdt1 is degraded and only geminin-GFP remains, giving cells green-fluorescent nuclei. During the G1/S transition, when Cdt1 levels are decreasing and geminin levels are increasing, both proteins are present, giving a yellow-fluorescent nuclear signal. This dynamic color change (red to yellow to green) clearly displays progression through the cell cycle and division.

Powered by BacMam 2.0 Technology
BacMam technology is based on an insect virus (baculovirus) for efficient transduction and transient expression in mammalian cells. The Premo? FUCCI cell cycle sensor uses BacMam 2.0 technology to enable cell cycle studies in essentially any cell type, from cell lines to stem cells by incorporation of a mammalian expression cassette for the FUCCI construct. Compared with BacMam 1.0 technology, BacMam 2.0 does not require the use of an enhancer and can be used in complete medium. There is no need to purify plasmid or worry about vector integrity and quality. No lipids, dye-loading chemicals, or other potentially harmful treatments are required. BacMam 2.0 incorporates elements that greatly enhance transduction efficiency and expression levels: a pseudotyped capsid protein for more efficient cell entry, an enhanced CMV promoter, and the Woodchuck hepatitis post-transcriptional regulatory element (WPRE).

Titratable Expression that Lasts Up to Two Weeks
The transient transgene expression lasts from about 5 days in transformed cell lines to up to two weeks in slowly dividing cells, such as some primary cell types; we have imaged terminally differentiated neurons more than three weeks after transduction. In addition, BacMam technology permits defined optimization because it gives you the ability to precisely titrate expression levels. Baculoviruses do not replicate in mammalian cells, nor are viral genes expressed, giving them an excellent safety profile and lack of cytopathic effects on mammalian cells.

Learn more about the Premo? FUCCI Cell Cycle Sensor

Reference:

1. Sakaue-Sawano A, Kurokawa H, Morimura T, Hanyu A, Hama H, Osawa H, Kashiwagi S, Fukami K, Miyata T, Miyoshi H, Imamura T, Ogawa M, Masai H, Miyawaki A. Visualizing spatiotemporal dynamics of multicellular cell-cycle progression. Cell. 2008 Feb 8;132(3):487-98. PubMed PMID: 18267078

Related products
We offer a range of BacMam-based reagents beyond CellLight? reagents, including the BacMam GFP Transduction Control that is ideal to test out the technology and optimize transduction conditions, Premo? Biosensors, including Premo? Autophagy Sensor, ion channel drug targets, pathway analysis kits, and more.

Learn more about these products and the BacMam technology

See other imaging tools and reagents

For Research Use Only. Not intended for any animal or human therapeutic or diagnostic use


規(guī)格

Color:Green,?Red-Orange
Delivery Method:Baculovirus (BacMam System)
Detection Method:Fluorescent
Emission Class:Visible
Excitation Class:Visible
Excitation?Emission (nm):488?510 (Green),?555?584 (Red)
For Use With (Equipment):Flow Cytometer,?Fluorescence Microscope,?Fluorescent Imager,?High Content Instrument,?Tali? Image-Based Cytometer
Form:Liquid
Label or Dye:GFP (EmGFP),?RFP (TagRFP)
Product Line:Premo?
Product Size:2 x 200 μL
Quantity:2 vials (200 μl each)
Sub-Cellular Localization:Nucleus
Technique:Fluorescence Intensity
Shipping Condition:Wet Ice


規(guī)格

Color:Green,?Red-Orange
Delivery Method:Baculovirus (BacMam System)
Detection Method:Fluorescent
Emission Class:Visible
Excitation Class:Visible
Excitation?Emission (nm):488?510 (Green),?555?584 (Red)
For Use With (Equipment):Flow Cytometer,?Fluorescence Microscope,?Fluorescent Imager,?High Content Instrument,?Tali? Image-Based Cytometer
Form:Liquid
Label or Dye:GFP (EmGFP),?RFP (TagRFP)
Product Line:Premo?
Product Size:2 x 200 μL
Quantity:2 vials (200 μl each)
Sub-Cellular Localization:Nucleus
Technique:Fluorescence Intensity
Shipping Condition:Wet Ice


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