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Mitotic Cells antibody

This anti- antibody is a Mouse Monoclonal antibody detecting in FACS, IHC (fro) and IF. Suitable for Human and Zebrafish (Danio rerio).
Catalog No. ABIN112395

Quick Overview for Mitotic Cells antibody (ABIN112395)

Target

Mitotic Cells

Reactivity

  • 4
  • 1
  • 1
Human, Zebrafish (Danio rerio)

Host

  • 4
Mouse

Clonality

  • 4
Monoclonal

Conjugate

  • 4
Un-conjugated

Application

  • 4
  • 2
  • 2
  • 1
  • 1
Flow Cytometry (FACS), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunofluorescence (IF)

Clone

8B3G
  • Cross-Reactivity (Details)

    Species reactivity (tested):Human, Zebrafish.

    Purification

    Immunoaffinity Chromatography

    Immunogen

    Total cell lysate of the human bladder carcinoma cell line T24.

    Isotype

    IgM
  • Application Notes

    This antibody is suitable for Flow cytometric analyses (1/50-1/100) andImmunocytochemistry with avidin-biotinylated horseradish peroxidase complex (ABC) asdetection reagent (1/50-1/100). Not suitable for Immunoblotting.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Restrictions

    For Research Use only
  • Concentration

    1.0 mg/mL

    Buffer

    PBS, 0.09 % Sodium Azide

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the lyophilized antibody at 2-8 °C for up to one month or at -20 °C for longer.
  • Target

    Mitotic Cells

    Background

    The life cycle of a eukaryotic cell consists of various phases, two of which can morphologically and biochemically be identified. Firstly, during mitosis (M-phase), in which the cell divides into two identical daughter cells, chromosome condensation and spindle formation are microscopically visible. Secondly, in S-phase the DNA of a cell is replicated, a process that can be detected using biochemical techniques, such as the BrdU incorporation assay. In between the M- and S-phase two gap phases occur: the G1-phase, the gap between mitosis and the start of DNA replication, and G2-phase, the gap between completion of DNA replication and the onset of mitosis. From G1-phase a cell can leave the cell cycle and enter G0, a 'quiescent' phase. Regulation of the cell cycle predominantly occurs at three major control points, which govern the transition from G0 to G1, from G1 to S, and from G2 to M-phase. M phase itself is highly regulated, and is divided into five stages: prophase, prometaphase, metaphase, telophase and anaphase.
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