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AB176748

Cell Viability Assay Kit (Fluorometric - Blue Ex 405 nm)

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(2 Publications)

Cell Viability Assay Kit (Fluorometric - Blue Ex 405 nm) (ab176748) uses a proprietary cell viability dye whose fluorescence is strongly enhanced upon entering into live cells.
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Functional Studies - Cell Viability Assay Kit (Fluorometric - Blue Ex 405 nm) (AB176748)
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Supplier Data

Functional Studies - Cell Viability Assay Kit (Fluorometric - Blue Ex 405 nm) (AB176748)

Excitation and Emission Spectra for Cell Viability Assay Kit (Fluorometric - Blue Ex 405 nm) (ab176748)

Functional Studies - Cell Viability Assay Kit (Fluorometric - Blue Ex 405 nm) (AB176748)
  • FuncS

Supplier Data

Functional Studies - Cell Viability Assay Kit (Fluorometric - Blue Ex 405 nm) (AB176748)

CHO-K1 cell number measured with Cell Viability Assay Kit (Flurometric-Blue Ex 405nm).

CHO-K1 cell number response was measured with Cell Viability Assay Kit (Fluorometric - Blue Ex 405 nm) (ab176748). CHO-K1 cells were seeded overnight at 0 - 5,000 cells/well/100 μL in a black wall/clear bottom 96-well plate. The cells were incubated with 100 μL/well of CytoCalcein Violet 450 dye-loading solution for 1 hour at room temperature. The fluorescence intensity was measured at Ex/Em = 405/460 nm. The fluorescence intensity was linear (R2 = 1) to the cell number as indicated.

The detection limit was 70 cells/well (n=6).

Key facts

Detection method

Fluorescent

Sample types

Suspension cells

Assay type

Cell-based

Results type

Quantitative

Assay Platform

Microplate reader, Fluor. microscope, Flow cyt.

Product details

Cell Viability Assay Kit (Fluorometric - Blue Ex 405 nm) (ab176748) uses a proprietary cell viability dye whose fluorescence is strongly enhanced upon entering into live cells.

The dye is a hydrophobic compound that easily permeates intact live cells. The weakly fluorescent CytoCalcein Violet 450, AM is hydrolyzed by intracellular esterase to generate a strongly fluorescent hydrophilic product that is well-retained in the cell cytoplasm.

The esterase activity is proportional to the number of viable cells, and thus directly related to the fluorescence intensity of the product generated from the esterase-catalyzed hydrolysis of the fluorogenic substrate.

Cells grown in black wall/clear bottom plates can be stained and quantified in less than two hours.

The assay is more robust than tetrazolium salt or Alamar Blue® based ones. It can be readily adapted for many different types of fluorescence platforms such as microplate assays, fluorescence microscope, and flow cytometry.

Review the to learn about more kits to perform a , and .

What's included?

{ "values": { "500Test": { "sellingSize": "500 Test", "publicAssetCode":"ab176748-500Test", "assetComponentDetails": [ { "size":"1 x 50 mL", "name":"Assay Buffer", "number":"AB176748-CMP01", "productcode":"" }, { "size":"5 x 1 Vial", "name":"CytoCalcein Violet 450, AM", "number":"AB176748-CMP02", "productcode":"" }, { "size":"1 x 200 µL", "name":"DMSO", "number":"AB176748-CMP03", "productcode":"" } ] } } }

Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
-20°C

Product protocols

Target data

Publications (2)

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ACS synthetic biology 13:3246-3255 PubMed39318128

2024

Optimization of Exon-Skipping Riboswitches and Their Applications to Control Mammalian Cell Fate.

Applications

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Yoko Nomura,Narae Kim,Bochen Zhu,Muhammad Hamzah,Haifeng Zhang,Yohei Yokobayashi

Biosensors & bioelectronics 183:113215 PubMed33845292

2021

Islet-on-a-chip: Biomimetic micropillar-based microfluidic system for three-dimensional pancreatic islet cell culture.

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Patrycja Sokolowska,Kamil Zukowski,Justyna Janikiewicz,Elzbieta Jastrzebska,Agnieszka Dobrzyn,Zbigniew Brzozka
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