CyQUANT™ Cell Proliferation Assays
CyQUANT™ Cell Proliferation Assays
Invitrogen™

CyQUANT™ Cell Proliferation Assays

CyQUANT cell proliferation assays are fast and highly sensitive fluorescence methods for counting cells to assess cell growth and cytotoxicity in microplate format. These assays use fluorescent nucleic-acid-binding dyes to measure cell number based on DNA content.
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產品號碼Cell TypeQuantity
C35006NF Cell1000 Assays
C35011Direct Cell10 Microplates
C35013Direct Red Cell10 Microplates
C35007NF Cell200 Assays
C7026For cells in culture1000 Assays
C7027Cell Lysis Buffer50 mL
產品號碼 C35006
價格 (HKD)
4,200.00
Each
新增至購物車
Cell Type:
NF Cell
Quantity:
1000 Assays
價格 (HKD)
4,200.00
Each
新增至購物車

Since the amount of DNA in cells is highly regulated, methods to detect DNA content offer improved accuracy over metabolism-based cellular proliferation or cytotoxicity assays, which can be affected by cell changes that are unrelated to cell number. CyQUANT cell proliferation assays use cell-permeant, DNA-binding dyes that enhance fluorescence when bound to nucleic acids to measure cellular DNA content. The resulting fluorescent signal can be compared to standards to determine cell number, enabling fast and sensitive microplate assays to measure cell proliferation and cytotoxicity.

Choose from a range of CyQUANT cell proliferation assays based on experimental needs and workflows.

The CyQUANT and CyQUANT NF (No Freeze) cell proliferation assays provide cell proliferation measurements based on the total cell count, including both live and dead cells. The CyQUANT Direct Cell Proliferation Assay only detects live, healthy cells by using a masking dye that blocks staining of dead cells with compromised membranes, providing measurement of both cellular proliferation and cytotoxicity.

CyQUANT Cell Proliferation Assay

The CyQUANT Cell Proliferation Assay (Cat. No. C7026) enables precise DNA measurement for total cell count using the green-fluorescent CyQUANT GR dye and allows for the convenient freezing and storage of samples for up to four weeks. Easily compare multiple samples with minimal hands-on time by freezing, lysing, and reading fluorescence on a standard microplate reader.

Features of the CyQUANT Cell Proliferation Assay include:

  • Direct DNA measurement

    —utilizes the green-fluorescent CyQUANT GR dye (ex/em 480/520 nm), a proprietary dye with strong fluorescence enhancement when bound to nucleic acids, for accurate measurement of DNA content to count both live and dead cells
  • Broad linear range

    —quantify 50 to 50,000 cells per well without relying on metabolic activity
  • Quickly compare samples

    —compare multiple samples in a microplate format with minimal hands-on time; simply remove media, freeze and lyse cells, then read fluorescence on a standard microplate reader with a fluorescein filter
  • Convenient sample storage

    —freeze and store time course samples for up to four weeks, enabling batch analysis and direct comparison of samples taken at different time points
  • Comprehensive kit

    —includes the CyQUANT GR dye, cell lysis buffer, and bacteriophage λ DNA as a reference standard; extra CyQUANT Cell Lysis Buffer available separately (Cat. No. C7027)

CyQUANT NF (No Freeze) Cell Proliferation Assay

The CyQUANT NF (No Freeze) Cell Proliferation Assay (Cat. Nos. C35006 and C35007) offers a streamlined protocol for total cell count by eliminating the freeze-thaw cell lysis step of the original CyQUANT Cell Proliferation Assay using a cell-permeant DNA-binding dye and a plasma membrane permeabilization/dye delivery reagent. This sensitive and rapid cell counting assay provides a wide detection range and is completed in just one hour without the need for cell lysis.

Features of the CyQUANT NF Cell Proliferation Assay include:

  • Streamlined protocol

    —eliminates the freeze-thaw cell lysis step using the cell-permeant and green-fluorescent CyQUANT NF DNA-binding dye (ex/em 480/520 nm) in combination with a plasma membrane permeabilization reagent for accurate measurement of DNA content to count both live and dead cells
  • Wide detection range

    —linear detection range from 100 to 20,000 cells per well in a 96-well microplate
  • Sensitive and rapid assay

    —more sensitive than MTT or alamarBlue™ assays, complete proliferation protocol in just one hour
  • No cell lysis required

    —eliminates the need for cell lysis, long incubations, radioactivity, or stain removal

CyQUANT Direct Cell Proliferation Assay

The CyQUANT Direct Cell Proliferation Assay (Cat. Nos. C35011, C35012, and C35013) provides a simple, no-wash, add-and-read workflow ideal for high-throughput screening cellular proliferation and cytotoxicity assays. This assay uses a green- or red-fluorescent cell-permeant DNA-binding probe that enters all cells and a cell-impermeant background suppressor that blocks staining in dead cells or cells with compromised membranes, ensuring that only live, healthy cells are stained. The assay measures changes in cell proliferation as well as cytotoxicity to allow for accurate assessment of cell growth, viability, and compound toxicity.

Features of the CyQUANT Direct Cell Proliferation Assay include:

  • Dual measurement

    —assesses both cell proliferation and membrane integrity, staining only live, viable cells
  • Convenient workflow

    —no washes, cell lysis, temperature equilibrations, or radioactivity required; ideal for high-throughput screening
  • Two fluorescent options

    —available in green CyQUANT Direct (ex/em 508/527 nm) and red CyQUANT Direct Red (ex/em 622/645 nm) for multiplexing with other fluorescent dyes or proteins; can switch between HTS and HCS plate readers if multiplex assays require different platforms
  • Wide detection range

    —linear detection from less than 100 to 20,000 cells per well in most cell types
  • Rapid and easy protocol

    —no-wash, homogeneous format with a fast proliferation protocol; simply mix the probe and suppressor, add to cells, incubate for one hour, and measure fluorescence
  • Stable signal

    —fluorescent signal remains stable for several hours, providing workflow flexibility
  • Multiplexing capability

    —compatible with spectrally distinct fluorescent probes or luminescence assays because cells are not lysed, allowing use with different platforms
  • Correlation with metabolic assays

    —excellent concordance with metabolism- or energy (ATP)-based cell health assays for reliable comparison of historical data
For Research Use Only. Not for use in diagnostic procedures.
規格
Cell TypeNF Cell
Detection MethodFluorescence
Dye TypeOther Label(s) or Dye(s)
Excitation/Emission480/520 nm
Format384-well plate, 96-well plate
Quantity1000 Assays
Shipping ConditionRoom Temperature
For Use With (Application)Proliferation Assay
For Use With (Equipment)Microplate Reader, HTS Reader
Product LineCyQUANT
Product TypeCell Proliferation Assay
Unit SizeEach
內容物與存放
•CyQUANT™ NF dye reagent
•Dye delivery reagent
•5X HBSS buffer (Hank’s balanced salt solution)

It is possible to observe precipitate in HBSS buffer. The precipitate does not have an impact on the use of this kit, nor the results that are gathered from its use.

常見問答集 (常見問題)

What is the difference between the original CyQuant assay and the CyQuant NF assay?

The original CyQUANT assay provides sensitive detection of cells over a 1000-fold linear dynamic range. In this assay, a freeze-thaw cell lysis step is required to facilitate the interaction of the CyQUANT GR dye with DNA. The CyQUANT NF assay avoids this freeze-thaw step by using a DNA binding dye in combination with a plasma membrane permeabilization reagent. The CyQUANT NF protocol requires only aspiration of growth medium (for adherent cells), replacement with dye binding solution, incubation for 30-60 minutes, and then measurement of fluorescence in a microplate reader. The assay is designed to produce a linear analytical response from at least 100-20,000 cells per well in most cell lines in a 96-well microplate.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Do you have spectral data for the CyQUANT NF Cell Proliferation Assay kit?

When CyQUANT NF dye is bound to DNA, the approximate excitation/emission is 480/520 nm. It can be detected using standard GFP or FITC filter settings.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Do you offer any products to measure neuronal cell health?

PrestoBlue Cell Viability Stain and CyQUANT Cell Proliferation Assay Kit can be used. We also offer a Neurite Outgrowth Staining Kit (Cat. No. A15001). More information about our different assays for neuronal cell health can be found here (https://www.thermofisher.com/us/en/home/life-science/cell-analysis/neuroscience/neuronal-cell-health-assays.html).

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

引用資料與參考文獻 (15)

引用資料與參考文獻
Abstract
KIF14 messenger RNA expression is independently prognostic for outcome in lung cancer.
Authors:Corson TW,Zhu CQ,Lau SK,Shepherd FA,Tsao MS,Gallie BL
Journal:Clinical cancer research : an official journal of the American Association for Cancer Research
PubMed ID:17545527
Functional symbiosis between endothelium and epithelial cells in glomeruli.
Authors:Hirschberg R, Wang S, Mitu GM,
Journal:Cell Tissue Res
PubMed ID:17999087
'In some capillary beds, pericytes regulate endothelial growth. Capillaries with high filtration capacity, such as those in renal glomeruli, lack pericytes. Glomerular endothelium lies adjacent to visceral epithelial cells (podocytes) that are anchored to and cover the anti-luminal surface of the basement membrane. We have tested the hypothesis that podocytes ... More
Flex-Hets differentially induce apoptosis in cancer over normal cells by directly targeting mitochondria.
Authors:Liu T, Hannafon B, Gill L, Kelly W, Benbrook D
Journal:Mol Cancer Ther
PubMed ID:17575110
'Flex-Het drugs induce apoptosis in multiple types of cancer cells, with little effect on normal cells. This apoptosis occurs through the intrinsic mitochondrial pathway accompanied by generation of reactive oxygen species (ROS). The objective of this study was to determine if direct or indirect targeting of mitochondria is responsible for ... More
Cytosolic delivery of membrane-impermeable molecules in dendritic cells using pH-responsive core-shell nanoparticles.
Authors:Hu Y, Litwin T, Nagaraja AR, Kwong B, Katz J, Watson N, Irvine DJ,
Journal:Nano Lett
PubMed ID:17887715
'Polycations that absorb protons in response to the acidification of endosomes can theoretically disrupt these vesicles via the "proton sponge" effect. To exploit this mechanism, we created nanoparticles with a segregated core-shell structure for efficient, noncytotoxic intracellular drug delivery. Cross-linked polymer nanoparticles were synthesized with a pH-responsive core and hydrophilic ... More
Decrease of endogenous vascular endothelial growth factor may not affect glioma cell proliferation and invasion.
Authors:Hong X, Jiang F, Kalkanis SN, Zhang ZG, Zhang X, Zheng X, Mikkelsen T, Jiang H, Chopp M
Journal:J Exp Ther Oncol
PubMed ID:17552362
'Vascular endothelial growth factor (VEGF) is abundantly produced by glioma cells especially glioblastoma, the most malignant form of astrocytoma. VEGF, a well known angiogenic factor, acts in a paracrine fashion on endothelial cells to develop tumor vasculature. However, recent studies have found that several tumor cells express VEGF receptors, and ... More