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Cells generate a complete set of proteins during cell division. Protein synthesis is essential in cell growth, proliferation, signaling, differentiation or death. Methods enabling detection and characterization of nascent proteins, or changes in protein expression/degradation during disease, drug treatments or environmental changes are vital in cytotoxicity studies. BioVision’s EZClick™ Protein Synthesis Monitoring Assay Kits can be used in different platforms by utilizing a novel and robust method based on an analog of puromycin, O-Propargyl-puromycin (OP-puro). OP-puro does not require methionine-free conditions and can be used to label nascent proteins directly in the cell culture. Our kits are simple, non-radioactive, sensitive, and can be used using a fluorescence microscope or a flow cytometry.


Key Features:

Non-radioactive, versatile assays (Flow cytometry and Fluorescence Microscopy)
Specific, homogeneous assay
Sensitive: fluorometric format
Convenient: minimal sample preparation, fast protocols (< 2 hours)
Cost effective: 50 assays; High Throughput Screening (HTS) compatible
Adaptable: works with most of the commonly available instrumentations

 

Figure. A. Analysis of protein biosynthesis in presence of Cycloheximide. Jurkat cells were pre-incubated (vehicle vs. 1X Cycloheximide, for 30 minutes at 37°C). Cells were then incubated either with culture medium (white), 1X EZClickTM  Protein Label (Red) or 1X Cycloheximide (Green) for 30 minutes. Protein synthesis was detected by Flow Cytometry (FL-2). Data shows the inhibitory effect of Cycloheximide on nascent polypeptides synthesis. B. Analysis of protein biosynthesis in presence of Cycloheximide. HeLa cells were pre-incubated (vehicle vs. 1X Cycloheximide;  30 minutes at 37°C). Cells were then incubated in culture medium containing 1X EZClickTM  Protein Label without or with 1X Cycloheximide. Protein synthesis was detected by Fluorescence Microscopy. Reduced red fluorescence in Cycloheximide shows its inhibitory effect on translation of mRNA to nascent polypeptides. Nuclear staining in both panels confirms that red fluorescence is the result of EZClickTM  Protein Label incorporation.

 

Check out BioVision’s kits evaluating cell proliferation, cell cytotoxicity & cell viability !

 

Product Name

Catalog

Size

EZClick™ EdU DNA Synthesis Monitoring Kit (FC)

K946

50 assays

EZClick™ EdU DNA Synthesis Monitoring Kit (M)

K947

50 assays

BrdU Cell Proliferation Assay Kit

K306

200 ,1000 assays

Cell Proliferation Assay Kit (F)

K307

1000 assays

EZClick™ Protein Synthesis Monitoring Assay Kit (FC)

K715

50 assays

EZClick™ Protein Synthesis Monitoring Assay Kit (M)

K714

100 assays

EZViable™ Calcein AM Cell Viability Assay Kit (F)

K305

1000 assays

MTS Cell Proliferation (C) Assay Kit

K300

500 , 2500 assays

MTT Cell Proliferation Assay Kit (C)

K299

1000 assays

Neutral Red Cell Cytotoxicity Assay Kit

K447

1000 assays

Quick Cell Proliferation (C) Assay Kit

K301

500 , 2500 assays

Quick Cell Proliferation (C) Assay Kit Plus

K302

500 , 2500 assays

Ready-to-use Cell Proliferation (C) Reagent, WST-1

K304

2500 assays

VisionBlue™ Quick Cell Viability (F) Assay kit 

K303

500 , 2500 assays

Adenylate Kinase (AK) Activity Assay Kit (C/F)

K350

100 assays

Cell-Mediated Cytotoxicity (F) Assay Kit (7-AAD/CFSE)

K315

100 assays

LDH-Cytotoxicity (C) Assay Kit

K311

400 assays

LDH-Cytotoxicity (C) Assay Kit II

K313

500 assays

PicoProbe™ LDH-Cytotoxicity (F) Assay Kit

K314

500 assays

Live-Dead Cell Staining Kit

K501

100 assays

Live/Dead Cell Viability Assay Kit(for Mammalian Cells)

K502

100 assays

Senescence Detection Kit

K320

250 assays

Senescence Detection Kit (F)

K991

100 assays

ApoSENSOR™ATP Cell Viability Bioluminescence Assay Kit

K254

200 , 1000 assays

ADP/ATP Ratio Biolumnescence Assay Kit, ApoSENSOR

K255

200 assays

Lactate Dehydrogenase Activity (C) Assay Kit

K726

500 assays

 *(FC)- Flow Cytometry, (M)-Microscopy, (F)-Fluorometric, (C)-Colorimetric

 

Check out our flyer Cell Viability, Proliferation & Cytotoxicity for information on related products.

 

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