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    products/elisa/cell-cycle-in-cell-elisa-kit-fluorescent-ab140363.pdf

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Cell Biology Cell Cycle Kinases/Phosphatases Cdks
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Cell Cycle In-Cell ELISA Kit (Fluorescent) (ab140363)

  • Datasheet
  • SDS
  • Protocol Booklet
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Antibody specificity demonstrated by Western Blot Analysis.
  • Sample data using ab140363 on HeLa cells treated with a titration of Hydroxyurea.
  • Sample experiment using ab140363 on HeLa cells treated with Paclitaxel and Hydroxyurea.

Key features and details

  • Assay type: Cell-based (quantitative)
  • Detection method: Fluorescent
  • Sample type: Adherent cells
  • Reacts with: Mouse, Human

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Overview

  • Product name

    Cell Cycle In-Cell ELISA Kit (Fluorescent)
  • Detection method

    Fluorescent
  • Sample type

    Adherent cells
  • Assay type

    Cell-based (quantitative)
  • Assay time

    6h 30m
  • Assay duration

    Multiple steps standard assay
  • Species reactivity

    Reacts with: Mouse, Human
  • Product overview

    ab140363 is an In-Cell ELISA (ICE) assay kit that uses quantitative immunocytochemistry to measure levels of Cdk2 protein phosphorylated Tyr15 and Histone H3 protein phosphorylated Ser10 levels in cultured cells. Cells are fixed in a microplate and targets of interest are detected with highly specific, well-characterized antibodies. Relative target levels are quantified using secondary antibodies conjugated to either horseradish peroxidase (HRP) or alkaline phosphatase (AP) which generate signal through the use of two spectrally distinct fluorogenic substrates. Fluorescence is measured using a standard fluorescent spectrophotometer and relative levels of target proteins are quantified. Optionally, antibody signal intensity can be normalized to the total cell amount using Janus Green stain. In-Cell ELISA (ICE) technique generates quantitative data with specificity similar to Western blotting, but with much greater quantitative precision and higher throughput due to the greater dynamic range and linearity of fluorescence detection and the ability to run up to 96 samples in parallel. This method rapidly fixes the cells in situ, stabilizing the in vivo levels of proteins and their post-translational modifications, and thus essentially eliminates changes during sample handling, such as preparation of protein extracts.

     

    Plates are available in our ICE (In-Cell ELISA) Support Pack (ab111542) which can be bought seperately.

  • Notes

    The Cdk2 (pTyr15) + Histone H3 (pSer10) In-Cell ELISA Kit (Fluorescent) (ab140363) is designed to study cell cycle effects in response to various stimuli. Monoclonal antibodies specific to Cdk2 (pTyr15) and Histone H3 (pSer10) are used in this high-throughput duplexing plate-based assay. Cdk2 (pTyr15) is elevated in G1/S phase of the cell cycle and Histone H3 (pSer10) is elevated in G2/M phase.
    Cyclin-dependent kinase 2 (Cdk2) is a nuclear protein kinase that functions in the G1/S phase of the cell cycle. Inhibitory phosphorylation occurs on residues Thr14 and Tyr15; activation of Cdk2 includes dephosphorylation of these residues by cdc25. Cdk2 can form a complex with Cyclin A, D or E. Phosphorylation of Cdk2 at Tyr15 indicates that a cell is at the G1/S transition.
    Histone H3 is one of the four core histone proteins (H2A, H2B, H3 and H4) that pack DNA in nucleosomes. Post-translational modifications of histones include phosphorylation and acetylation and are important for chromatin assembly and gene expression. Phosphorylation of Histone H3 at Ser10 is tightly correlated with chromosome condensation during mitosis. Hence, Histone H3 pSer10 signal indicates a mitotic cell with condensed DNA.
    In-Cell ELISA (ICE) technology is used to perform quantitative immunocytochemistry of cultured cells using enzyme linked secondary antibodies and fluorogenic substrates. The technique generates quantitative data with specificity similar to western blotting, but with much greater quantitative precision and higher throughput due to the greater dynamic range and linearity of fluorescence detection and the ability to run up to 96 samples in parallel. Because the Cdk2 (pTyr15) antibody is a rabbit antibody and the Histone H3 (pSer10) antibody is a mouse antibody, they can be measured simultaneously in the same well using the cocktail of provided primary antibodies, species-specific secondary antibodies and fluorogenic substrates. This method rapidly fixes the cells in situ, stabilizing the in vivo levels of proteins and their post-translational modifications, and thus eliminating changes during sample handling, such as in the preparation of protein extracts. Finally, the Cdk2 (pTyr15) and Histone H3 (pSer10) signals can be normalized to cell amount, measured by the provided Janus Green whole cell stain, to further increase the assay precision.

    Abcam has not and does not intend to apply for the REACH Authorisation of customers’ uses of products that contain European Authorisation list (Annex XIV) substances.
    It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

  • Platform

    Microplate

Properties

  • Storage instructions

    Store at +4°C. Please refer to protocols.
  • Components 1 x 96 tests
    1000X Anti-Mouse IgG/AP-Labeled Secondary Antibody 1 x 20µl
    1000X Anti-Rabbit IgG/HRP-Labeled Secondary Antibody 1 x 20µl
    100X Anti- Histone H3 (pSer10) Primary Antibody 1 x 120µl
    100X Anti-Cdk2 (pTyr15) Primary Antibody 1 x 120µl
    100X Triton X-100 1 x 500µl
    10X Blocking Solution 1 x 10ml
    10X Phosphate Buffered Saline 1 x 100ml
    10X Quenching Solution 1 x 1.5ml
    400X Fluorescent Substrate Cocktail 1 x 50µl
    400X Tween-20 1 x 2ml
    8000X Hydrogen Peroxide 1 x 50µl
    Fluorescent Substrate Buffer 1 x 12ml
    1X Janus Green Stain 1 x 17ml
  • Research areas

    • Cell Biology
    • Cell Cycle
    • Kinases/Phosphatases
    • Cdks
    • Epigenetics and Nuclear Signaling
    • Histones
    • H3
    • Unmodified
    • Signal Transduction
    • Protein Phosphorylation
    • Ser / Thr Kinases
    • Other Kinases
    • Epigenetics and Nuclear Signaling
    • Cell cycle
    • Kinases/Phosphatases
    • Cdks
    • Cancer
    • Cell cycle
    • Kinases/phosphatases
    • Cdks
    • Kits/ Lysates/ Other
    • Kits
    • ELISA Kits
    • ELISA Kits
    • Cell cycle proteins ELISA kits
  • Cellular localization

    Cytoplasmic and Nuclear
  • Alternative names

    • Cell division protein kinase 2
    • H3.3A
    • H3F3
    • H3F3A
    • H3F3B
    • Histone H3.3
    • p33 protein kinase
    see all
  • Database links

    • Entrez Gene: 1017 Human
    • Entrez Gene: 3020 Human
    • Entrez Gene: 12566 Mouse
    • Entrez Gene: 15078 Mouse
    • Entrez Gene: 15081 Mouse
    • Omim: 116953 Human
    • Omim: 601058 Human
    • Omim: 601128 Human
    • SwissProt: P24941 Human
    • SwissProt: P84243 Human
    • SwissProt: P97377 Mouse
    • SwissProt: P84244 Mouse
    see all

Associated products

  • Related Products

    • Cell Cycle (pCdk/pHH3/Actin) WB Cocktail (ab136810)
    • Cell Cycle and Apoptosis WB Cocktail (pCdk/pHH3/Actin/PARP) (ab139417)

Images

  • Antibody specificity demonstrated by Western Blot Analysis.
    Antibody specificity demonstrated by Western Blot Analysis.
    Whole cell lysates from HeLa cells were analyzed by Western blot with the primary antibodies used in this assay kit.
    (A) Histone H3 pSer10 antibody:
    Lane 1 -Untreated,
    Lane 2- hydroxyurea = G1/S arrest,
    Lane 3- paclitaxel = G2/M arrest .
    (B) Cdk2 pTyr15 antibody:
    Lane 1 -Untreated,
    Lane 2-, thymidine = G1/S arrest,
    Lane 3- nocodazole = G2/M arrest.
  • Sample data using ab140363 on HeLa cells treated with a titration of Hydroxyurea.
    Sample data using ab140363 on HeLa cells treated with a titration of Hydroxyurea.
    Data shown is for 24 hour treatment with 1.6 – 5000 nM hydroxyurea. Cdk2 pTyr15 intensity increases with hydroxyurea treatment dose whereas Histone H3 pSer10 intensity decreases.
  • Sample experiment using ab140363 on HeLa cells treated with Paclitaxel and Hydroxyurea.
    Sample experiment using ab140363 on HeLa cells treated with Paclitaxel and Hydroxyurea.
    Data shown is for 24 hour treatment with 1 mM hydroxyurea, 333 nM paclitaxel and untreated (Control). (Normalized intensity is described in section 9.)

Protocols

  • Protocol Booklet

Click here to view the general protocols

Datasheets and documents

  • SDS download

  • Datasheet download

    Download

References (4)

Publishing research using ab140363? Please let us know so that we can cite the reference in this datasheet.

ab140363 has been referenced in 4 publications.

  • Carpi S  et al. miRNA Modulation and Antitumor Activity by the Extra-Virgin Olive Oil Polyphenol Oleacein in Human Melanoma Cells. Front Pharmacol 11:574317 (2020). PubMed: 33071785
  • Ponandai-Srinivasan S  et al. Mifepristone mediates anti-proliferative effect on ovarian mesenchymal stem/stromal cells from female BRCA1-/2- carriers. Acta Obstet Gynecol Scand 98:250-261 (2019). PubMed: 30325501
  • Shcherbakov D  et al. Ribosomal mistranslation leads to silencing of the unfolded protein response and increased mitochondrial biogenesis. Commun Biol 2:381 (2019). PubMed: 31637312
  • Tiwari KK  et al. Differential concentration-specific effects of caffeine on cell viability, oxidative stress, and cell cycle in pulmonary oxygen toxicity in vitro. Biochem Biophys Res Commun 450:1345-50 (2014). PubMed: 24997337

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