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1
2019 - 03 - 08
1 月 28 日,国际学术期刊 Circulation Research 在线发表了中国科学院上海营养与健康研究所宗耕课题组与哈佛大学公共卫生学院营养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”。该研究发现较高的植物来源单不饱和脂肪酸(MUFA-Ps)摄入量与较低的总死亡率相关,而动物来源单不饱和脂肪酸(MUFA-As)的摄入则与较高死亡率相关。另外,用植物来源单不饱和脂肪酸替代饱和脂肪酸(SFAs)、精加工的碳水化合物或反式脂肪可以显著降低死亡风险。在全球范围内,心血管疾病(CVD)和癌症是造成过早死亡的最主要原因。目前,越来越多的研究表明采取健康的生活方式(如戒烟、增加体力活动和提高膳食质量等)能够有效降低过早死亡的风险。多个国家的膳食指南均强调了膳食脂肪的质量对预防慢性疾病的重要性,尤其提倡植物油及其他植物来源的脂肪摄入。例如,膳食中的多不饱和脂肪酸(PUFAs)主要来自植物,而现有的研究表明 PUFAs 能够降低心血管疾病风险和死亡率的关系。与之相比,饮食中的单不饱和脂肪酸只有一半来自植物油(尤其...
2
2019 - 07 - 05
据新华社电 美国疾病控制和预防中心研究团队发现,正在刚果(金)使用的两种试验性疗法对抗击当前的埃博拉疫情有效。7 月 9 日发表在英国《柳叶刀—传染病》杂志上的研究显示,在实验室中,抗病毒药物 Remdesivir,以及由三种抗体组成的抗埃博拉药物 ZMapp 可阻断新一轮埃博拉疫情的致病毒株在人类细胞中增长。确认抗病毒药物有效的关键之一在于找到此次疫情的致病毒株。论文第一作者、美疾控中心微生物学家劳拉 · 麦克马伦说,目前在刚果(金)试用的疗法均针对以前疫情中获取的埃博拉毒株,而埃博拉是一种核糖核酸(RNA)病毒,会不断变异,因此确定现有疗法是否对新毒株奏效至关重要。美疾控中心研究人员没有当前在刚果(金)传播的 “伊图里” 毒株样本,但他们从开源基因库中获得病毒序列数据,使用 “反向遗传学” 技术重组了毒株。这项技术有助于研究人员更多了解新毒株在埃博拉家族树中的位置,从而寻找更多潜在疗法,并测试各类新疗法的有效性,还可与未来的新毒株进行比对。研究中还发现,2014 年到 2016 年西非多国爆发埃博拉疫情期间开发的一种实验室病毒诊断方法可用于诊断 “伊图里” 毒株。(周舟)文章摘自:生物360
3
2020 - 02 - 21
2020年2月16日讯 /生物谷BIOON /--国家指南建议前列腺癌患者多吃蔬菜,这可能会减少癌症的进展和死亡。但在一项III期随机临床试验中,前列腺癌患者被指定每天吃7份或更多的蔬菜和水果,却没有发现额外的微量营养元素摄入的保护作用。'这些数据表明,尽管科学和公众舆论普遍认为需要吃蔬菜,但多吃蔬菜缺确实不会改变前列腺癌的病程。据我们所知,它不会抑制或治愈它。然而,虽然多吃水果和蔬菜的健康饮食和多做运动不一定能治愈癌症,但它可能使身体更强壮、更健康,这可能有助于患者忍受癌症治疗。'图片来源:Wikipedia这项研究近日发表在《Journal of the American Medical Association》上,,由加州大学圣地亚哥分校Moores癌症中心和Roswell Park综合癌症中心的研究人员完成,招收了478名年龄在50到80岁男性。这些患者被诊断为早期前列腺腺癌,并参与了一个积极的监测项目,在该项目中,患者推迟立即治疗,直到病情恶化。患者被随机分为两组,一组接受关于饮食和前列腺癌的书面信息,另一组接受电话咨询的行为干预项目,该项目鼓励参与者食用类胡萝卜素含量高的食物,如绿叶蔬菜、胡萝卜和西红柿,以及十字花科蔬菜,如西兰花和卷心菜。两组都接受了两年的监测。被分配到干预组的患者增加了水果和蔬菜的摄入量,达到了有统计学意义的程度,明显多于对照组患者。...
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产品名称:

LIVE/DEAD™ Fixable Green Dead Cell Stain Kit, for 488 nm excitation

上市日期: 2019-04-22
产品类别: INVITROGEN

规格

Compatible Cells:Eukaryotic Cells
For Use With (Equipment):Flow Cytometer
Detection Method:Fluorescent
Format:Tube(s)
Excitation⁄Emission (nm):495⁄520
Flow Cytometer Laser Lines:488
Form:Solid
Label or Dye:LIVE/DEAD® Fixable Green Dead Cell Stain
Number of Reactions:200
Product Line:LIVE/DEAD®
Product Size:200 assays
Solubility:DMSO (Dimethylsulfoxide)
Shipping Condition:Room Temperature


  • 产品描述
  • 产品功能
  • 产品参数

描述

The LIVE/DEAD™ Fixable Green Dead Cell Stain Kit is used to determine the viability of cells prior to the fixation and permeabilization required for intracellular antibody staining or prior to elimination of biohazardous materials using formaldehyde fixation. This kit has been optimized and validated for use with a blue laser flow cytometer.

• Stable—dyes are freeze dried in separate vials to maintain stability
• Robust—staining pattern is the same before and after fixation
• Bright signal—allows for easy distinction between live/dead cells in single channel

View a selection guide for all fixable viability dyes for flow cytometry.

Stable
Unlike products that are sold in solution, the LIVE/DEAD™ Fixable Green Stain has been conveniently packaged in 40-test vials to help ensure the stability and performance of the dye over time. Amine reactive dyes in solution will lose their effectiveness over a short period of time, therefore it is recommended to completely use the vial once rehydrated. If this is not possible, aliquot the vials in small volumes and store at -80°C, avoiding freeze-thaw cycles.

Robust
Dead cell discriminator stains can lose sensitivity after treatment with fixatives such as formaldehyde or ethanol-based fixation methods required for intracellular phosphorylation studies. The LIVE/DEAD™ Fixable Green Stain is an amine reactive dye that binds covalently to intracellular and extracellular amines, and the staining pattern is preserved following formaldehyde fixation.

Optimal brightness
The LIVE/DEAD™ Fixable Green stain was selected based on its fluorescent properties to provide a bright signal when excited with a blue 488 nm laser. The green-fluorescent reactive dye has an excitation maximum of ~495 nm making it ideal for use with the blue laser and an emission of ~520 nm allowing collection in the FITC channel. Since live and dead cells can be discriminated using a single dye and a single channel of a flow cytometer, it is an ideal choice for multi-color experiments.

How it works
In cells with compromised membranes, the dye reacts with free amines both in the cell interior and on the cell surface, yielding intense fluorescent staining. In viable cells, the dye's reactivity is restricted to the cell-surface amines, resulting in less intense fluorescence. The difference in intensity is typically greater than 50-fold between live and dead cells, allowing for easy discrimination.

Colors available
LIVE/DEAD™ Fixable Dead Cell Stains are available in a wide variety of colors to meet your multi-color panel needs.


规格

Compatible Cells:Eukaryotic Cells
For Use With (Equipment):Flow Cytometer
Detection Method:Fluorescent
Format:Tube(s)
Excitation⁄Emission (nm):495⁄520
Flow Cytometer Laser Lines:488
Form:Solid
Label or Dye:LIVE/DEAD® Fixable Green Dead Cell Stain
Number of Reactions:200
Product Line:LIVE/DEAD®
Product Size:200 assays
Solubility:DMSO (Dimethylsulfoxide)
Shipping Condition:Room Temperature


规格

Compatible Cells:Eukaryotic Cells
For Use With (Equipment):Flow Cytometer
Detection Method:Fluorescent
Format:Tube(s)
Excitation⁄Emission (nm):495⁄520
Flow Cytometer Laser Lines:488
Form:Solid
Label or Dye:LIVE/DEAD® Fixable Green Dead Cell Stain
Number of Reactions:200
Product Line:LIVE/DEAD®
Product Size:200 assays
Solubility:DMSO (Dimethylsulfoxide)
Shipping Condition:Room Temperature


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