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1
2019 - 01 - 07
2019年1月7日 讯 /生物谷BIOON/ --诱发癌症有很多遗传原因,比如有些突变会遗传自父母,而其它则是后天获得性的突变,比如因外界因素或DNA复制的错误导致等,大规模的基因组测序在识别因体细胞突变所诱发的癌症上取得了一系列研究成果,但这种技术却无法有效识别因遗传性突变所诱发的癌症,而且识别这些遗传突变的主要来源仍然是基于家族性的研究。图片来源:iran-daily.com近日,一项刊登在国际杂志Nature Communications上的研究报告中,来自巴塞罗那基因组研究中心的科学家们通过研究开发了一种新型的统计学方法,其能够从肿瘤测序数据中鉴别出癌症易感性基因;该方法使用了一种古老的想法,即癌基因通常需要“两次击打”(two hits)才能够致癌,研究者表示,这种方法能帮助他们从当前癌症基因组数据库中系统性地鉴别出相关的基因。研究者将这种统计学方法命名为“ALFRED”,目前该技术已经鉴别出了13个候选的癌症易感性基因,其中10个基因都是此前并未发现的;Ben Lehner博士说道,我们对30种不同类型的肿瘤患者进行研究,将这种方法应用于1万多名患者的基因组序列中,最终鉴别出了已知的和一些新型的可能性癌症易感基因,这些基因有可能会诱发一定的患癌风险。研究者指出,新型的癌症易感基因或许在多种类型癌症的发生上扮演着关键角色,比如,其与14%的卵巢肿瘤、1%的乳腺癌等癌症直接...
2
2019 - 05 - 27
5月24日,记者从中国农业科学院科研进展通报会上获悉,由中国农业科学院哈尔滨兽医研究所(以下称哈兽研)自主研发的非洲猪瘟疫苗取得了阶段性成果,实验室研究结果表明,具有良好的生物安全性和免疫保护效果。非洲猪瘟疫苗科研攻关负责人介绍,目前在非洲猪瘟疫苗创制阶段主要取得五项进展:一是分离我国第一株非洲猪瘟病毒。建立了病毒细胞分离及培养系统和动物感染模型,对其感染性、致病力和传播能力等生物学特性进行了较为系统的研究,并揭示了我国非洲猪瘟流行毒株的基因组特点和进化关系。二是创制了非洲猪瘟候选疫苗,实验室阶段研究证明其中两个候选疫苗株具有良好的生物安全性和免疫保护效果。三是两种候选疫苗株体外和体内遗传稳定性强。分别将两种候选疫苗株在体外原代细胞中连续传代,其生物学特性及基因组序列无明显改变,猪体内连续传代,也未发现明显毒力返强现象。四是明确了最小保护接种剂量,证明大剂量和重复剂量接种安全。五是临床前中试产品工艺研究初步完成。目前已建立两种候选疫苗的生产种子库,初步完成了疫苗生产种子批纯净性及外源病毒检验,初步优化了候选疫苗的细胞培养及冻干工艺。非洲猪瘟疫情发生后,党中央、国务院高度重视疫情防控科研攻关。中国农科院科技局局长任天志介绍,按照农业农村部党组统一部署,中国农科院将非洲猪瘟防控作为服务国家战略需求的重大科研攻关任务,集聚优势资源,第一时间组建非洲猪瘟防控科技攻关项目组,以哈尔滨兽医研究...
3
2019 - 11 - 08
“5年后的今天,他们中将只剩下3名幸存者。”在谈到不久前刚刚接触过的100名胶质母细胞瘤(GBM)新患者时,Howard Fine博士语气很低沉,也透着几许无奈。作为威尔康奈尔医学院(Weill Cornell Medicine)的一名肿瘤学家,从医30年来,Howard Fine博士曾治疗过不下两万名GBM患者,不过,最终的结果却很扎心——“你现在很难再看到这些人了,因为他们基本上都死了。”Howard Fine博士所经历的,正是GBM在现实生活中的真实写照。神经胶质瘤是最常见的恶性原发性脑瘤,占所有原发性脑瘤的近四分之一,占所有恶性肿瘤的四分之三;而GBM又是最常见、最具侵袭性的胶质瘤类型,占所有胶质瘤的一半以上,仅在美国,每年就有约1.2万个新发病例。GBM是一个“致命杀手”,一旦被确诊,留给患者的时间平均只剩下15个月左右。GBM如此冷酷无情,自然惹得天怒人怨、人人喊打,不过,一个非常尴尬的事实却是:在与它的交锋中,医学界推出的各种手段胜绩寥寥,一种 “有心杀贼,无力回天”的感觉油然而生。面对GBM的嚣张气焰,专注于开发创新癌症疗法的DelMar Pharmaceuticals公司“明知山有虎,偏向虎山行”,开发出了一种对抗GBM的有力武器——VAL-083。接下来,DelMar Pharmaceuticals总裁兼首席执行官Saiid Zarrabian先生将为我们讲述V...
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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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