merck millipore,默克密理博,17-10220,LentiBrite ™ RFP-Rad51 Lentiviral Biosensor

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merck millipore,默克密理博,17-10220,LentiBrite ™ RFP-Rad51 Lentiviral Biosensor
产品名称：LentiBrite ™ RFP-Rad51 Lentiviral Biosensor
产品型号：17-10220

merck millipore,默克密理博,17-10220,LentiBrite ™ RFP-Rad51 Lentiviral Biosensor

产品介绍

merck millipore,默克密理博,17-10220,LentiBrite ™ RFP-Rad51 Lentiviral Biosensor

重要规格表

主要应用	检测方法
ICC	Fluorescent

描述
产品目录编号	17-10220
商名	Chemicon LentiBrite
描述	LentiBrite ™ RFP-Rad51 Lentiviral Biosensor
概述	*Read our application note in Nature Methods!* Biosensors can be used to detect the presence/absence of a particular protein as well as the subcellular location of that protein within the live state of a cell. Fluorescent tags are often desired as a means to visualize the protein of interest within a cell by either fluorescent microscopy or time-lapse video capture. Visualizing live cells without disruption allows researchers to observe cellular conditions in real time. Lentiviral vector systems are a popular research tool used to introduce gene products into cells. Lentiviral transfection has advantages over non-viral methods such as chemical-based transfection including higher-efficiency transfection of dividing and non-dividing cells, long-term stable expression of the transgene, and low immunogenicity. EMD Millipore is introducing LentiBrite™ Lentiviral Biosensors, a new suite of pre-packaged lentiviral particles encoding important and foundational proteins of autophagy, apoptosis, and cell structure for visualization under different cell/disease states in live cell and in vitro analysis. Pre-packaged, fluorescently-tagged with GFP & RFP Higher efficiency transfection as compared to traditional chemical-based and other non-viral-based transfection methods Ability to transfect dividing, non-dividing, and difficult-to-transfect cell types, such as primary cells or stem cells Non-disruptive towards cellular function EMD Millipore’s LentiBrite™ RFP-Rad51 lentiviral particles provide bright fluorescence and precise localization to enable live cell analysis of Rad51 translocation in difficult-to-transfect cell types.
背景信息	Rad51, a eukaryotic RecA-like recombinase, plays a key role in homologous recombination occurring in both the normal cell cycle and repair of DNA damage. However, excess cellular Rad51, as occurs in many cancers, leads to resistance to DNA-damaging radiation and chemotherapy, and genomic instability. Upon DNA damage generating double strand breaks, Rad51 coalesces from the nucleoplasm to discrete nuclear foci, but such foci also occur in the absence of DNA damage when Rad51 is overexpressed. Expression of Rad51 fused to GFP has been employed to trace the dynamics of Rad51 compartmentalization in live cells. EMD Millipore’s LentiBrite™ RFP-Rad51 lentiviral particles provide bright fluorescence and precise localization to enable live cell analysis of Rad51 translocation in difficult-to-transfect cell types.

产品信息
部件	Multiplicty of Infection (MOI) MOI = Ratio of # of infectious lentiviral particles (IFU) to # of cells being infected. Typical MOI values for high transduction efficiency and signal intensity are in the range of 20-40. For this target, some cell types may require lower MOIs (e.g., HT-1080, HeLa, U2OS, human mesenchymal stem cells (HuMSC)), while others may require higher MOIs (e.g., human umbilical vein endothelial cells (HUVEC)). NOTE: MOI should be titrated and optimized by the end user for each cell type and lentiviral target to achieve desired transduction efficiency and signal intensity. TagRFP-Rad51 Lentivirus: One vial containing 25 µL of lentiviral particles at a minimum of 3 x 10E8 infectious units (IFU) per mL. For lot-specific titer information, please see “Viral Titer” in the datasheet. Promoter EF-1 (Elongation Factor-1)
检测方法	Fluorescent

产品信息

部件

Multiplicty of Infection (MOI)
MOI = Ratio of # of infectious lentiviral particles (IFU) to # of cells being infected.
Typical MOI values for high transduction efficiency and signal intensity are in the range of 20-40. For this target, some cell types may require lower MOIs (e.g., HT-1080, HeLa, U2OS, human mesenchymal stem cells (HuMSC)), while others may require higher MOIs (e.g., human umbilical vein endothelial cells (HUVEC)).
NOTE: MOI should be titrated and optimized by the end user for each cell type and lentiviral target to achieve desired transduction efficiency and signal intensity.
TagRFP-Rad51 Lentivirus:
One vial containing 25 µL of lentiviral particles at a minimum of 3 x 10E8 infectious units (IFU) per mL. For lot-specific titer information, please see “Viral Titer” in the datasheet.
Promoter
EF-1 (Elongation Factor-1)

检测方法

Fluorescent

应用
主要应用	Immunocytochemistry
应用说明	Fluorescence Microscopy Imaging: HeLa cells were plated in a chamber slide and transduced with lentiviral particles at an MOI of 20 for 24 hours. After media replacement and 48 hours further incubation, cells were fixed with formaldehyde and mounted. Images were obtained by oil immersion wide-field fluorescence microscopy. The RFP-Rad51 displays a variably punctate distribution in the nucleus. Immunocytochemistry Comparison: U2OS cells were plated in a chamber slide and transduced with lentiviral particles at an MOI of 5 for 24 hours. After 24 hours, media was replaced and cells were then further incubated for 48 hours. Immunocytochemical staining (green) with a polyclonal antibody against Rad51 (Cat No. ABE257) reveals a similar expression pattern to RFP-Rad51 (red). Hard-to-transfect Cell Types: Primary cell types HUVEC or HuMSC were plated in chamber slides and transduced with RFP-Rad51 lentiviral particles at an MOI of 20 and 5, respectively, for 24 hours. Confocal Microscopy Imaging: U2OS cells were transduced with RFP-Rad51 lentivirus. Cells were counterstained with FITC-phalloidin to show the actin filaments (green) and DAPI to show the nucleus (blue). Images were obtained by oil immersion confocal fluorescence microscopy. Additional Cell Type: HT1080 cells were treated. For optimal fluorescent visualization, it is recommended to analyze the target expression level within 24-48 hrs after transfection/infection for optimal live cell analysis, as fluorescent intensity may dim over time, especially in difficult-to-transfect cell lines. Infected cells may be frozen down after successful transfection/infection and thawed in culture to retain positive fluorescent expression beyond 24-48 hrs. Length and intensity of fluorescent expression varies between cell lines. Higher MOIs may be required for difficult-to-transfect cell lines.

应用

主要应用

Immunocytochemistry

应用说明

Fluorescence Microscopy Imaging:
HeLa cells were plated in a chamber slide and transduced with lentiviral particles at an MOI of 20 for 24 hours. After media replacement and 48 hours further incubation, cells were fixed with formaldehyde and mounted. Images were obtained by oil immersion wide-field fluorescence microscopy. The RFP-Rad51 displays a variably punctate distribution in the nucleus.

Immunocytochemistry Comparison:
U2OS cells were plated in a chamber slide and transduced with lentiviral particles at an MOI of 5 for 24 hours. After 24 hours, media was replaced and cells were then further incubated for 48 hours. Immunocytochemical staining (green) with a polyclonal antibody against Rad51 (Cat No. ABE257) reveals a similar expression pattern to RFP-Rad51 (red).

Hard-to-transfect Cell Types:
Primary cell types HUVEC or HuMSC were plated in chamber slides and transduced with RFP-Rad51 lentiviral particles at an MOI of 20 and 5, respectively, for 24 hours.

Confocal Microscopy Imaging:
U2OS cells were transduced with RFP-Rad51 lentivirus. Cells were counterstained with FITC-phalloidin to show the actin filaments (green) and DAPI to show the nucleus (blue). Images were obtained by oil immersion confocal fluorescence microscopy.

Additional Cell Type:
HT1080 cells were treated.

For optimal fluorescent visualization, it is recommended to analyze the target expression level within 24-48 hrs after transfection/infection for optimal live cell analysis, as fluorescent intensity may dim over time, especially in difficult-to-transfect cell lines. Infected cells may be frozen down after successful transfection/infection and thawed in culture to retain positive fluorescent expression beyond 24-48 hrs. Length and intensity of fluorescent expression varies between cell lines. Higher MOIs may be required for difficult-to-transfect cell lines.

生物信息
纯化方法	PEG precipitation
UniProt编号	Q06609

产品使用声明
质量保证	Evaluated by transduction of HT-1080 cells and fluorescent imaging performed for assessment of transduction efficiency.
使用声明	Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals. This product contains genetically modified organisms (GMO). Within the EU GMOs are regulated by Directives 2001/18/EC and 2009/41/EC of the European Parliament and of the Council and their national implementation in the member States respectively. This legislation obliges Merck-Millipore to request certain information about you and the establishment where the GMOs are being handled.

产品使用声明

质量保证

Evaluated by transduction of HT-1080 cells and fluorescent imaging performed for assessment of transduction efficiency.

使用声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
This product contains genetically modified organisms (GMO). Within the EU GMOs are regulated by Directives 2001/18/EC and 2009/41/EC of the European Parliament and of the Council and their national implementation in the member States respectively. This legislation obliges Merck-Millipore to request certain information about you and the establishment where the GMOs are being handled.

储存和货运信息
存储条件	Storage and Handling Lentivirus is stable for at least 4 months from date of receipt when stored at -80°C. After first thaw, place immediately on ice and freeze in working aliquots at -80°C. Frozen aliquots may be stored for at least 2 months. Further freeze/thaws may result in decreased virus titer and transduction efficiency. IMPORTANT SAFETY NOTE Replication-defective lentiviral vectors, such as the 3rd Generation vector provided in this product, are not known to cause any diseases in humans or animals. However, lentiviruses can integrate into the host cell genome and thus pose some risk of insertional mutagenesis. Material is a Risk Group 2 and should be handled under BSL2 controls. A detailed discussion of biosafety of lentiviral vectors is provided in Pauwels, K. et al. (2009). State-of-the-art lentiviral vectors for research use: Risk assessment and biosafety recommendations. Curr. Gene Ther. 9: 459-474.

储存和货运信息

存储条件

Storage and Handling
Lentivirus is stable for at least 4 months from date of receipt when stored at -80°C. After first thaw, place immediately on ice and freeze in working aliquots at -80°C. Frozen aliquots may be stored for at least 2 months. Further freeze/thaws may result in decreased virus titer and transduction efficiency.

IMPORTANT SAFETY NOTE
Replication-defective lentiviral vectors, such as the 3rd Generation vector provided in this product, are not known to cause any diseases in humans or animals. However, lentiviruses can integrate into the host cell genome and thus pose some risk of insertional mutagenesis. Material is a Risk Group 2 and should be handled under BSL2 controls. A detailed discussion of biosafety of lentiviral vectors is provided in Pauwels, K. et al. (2009). State-of-the-art lentiviral vectors for research use: Risk assessment and biosafety recommendations. Curr. Gene Ther. 9: 459-474.