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FOXM1 antibody (AA 48-763)

The Rabbit Polyclonal anti-FOXM1 antibody is suitable to detect FOXM1 in samples from Human, Rat and Mouse. It has been validated for WB, ELISA, ICC, IF and FACS.
Catalog No. ABIN7875216
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for FOXM1 antibody (AA 48-763) (ABIN7875216)

Target

See all FOXM1 Antibodies
FOXM1 (Forkhead Box M1 (FOXM1))

Reactivity

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Human, Rat, Mouse

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This FOXM1 antibody is un-conjugated

Application

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Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunofluorescence (IF), Flow Cytometry (FACS)
  • Binding Specificity

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    AA 48-763

    Purpose

    FOXM1 Antibody / Forkhead box protein M1

    Purification

    Immunogen affinity purified

    Immunogen

    E.coli-derived human FOXM1 recombinant protein (Position: K48-Q763) was used as the immunogen for the FOXM1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the FOXM1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the FOXM1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    FOXM1 (Forkhead Box M1 (FOXM1))

    Alternative Name

    FOXM1

    Background

    FOXM1 antibody detects Forkhead box protein M1, encoded by the FOXM1 gene on chromosome 12p13.33. FOXM1 antibody is widely used in studies of cell cycle regulation, transcription, and cancer biology. FOXM1 is a member of the forkhead box (FOX) family of transcription factors, characterized by a conserved winged-helix DNA-binding domain. It plays critical roles in G1/S and G2/M transitions of the cell cycle, controlling genes required for DNA replication, mitosis, and cytokinesis. Expression is high in proliferating cells and embryonic tissues, but normally downregulated in differentiated, non-dividing cells.

    Structurally, FOXM1 contains an N-terminal repressor domain, a central forkhead DNA-binding domain, and a C-terminal transactivation domain. Its activity is regulated by phosphorylation, with cyclin-CDK complexes and MAPKs activating FOXM1 during the cell cycle. Alternative splicing produces isoforms with distinct transcriptional activities, including FOXM1a (inactive), FOXM1b, and FOXM1c (active in proliferation).

    Functionally, FOXM1 drives expression of cell cycle regulators such as cyclin B1, cyclin D1, PLK1, and Aurora B kinase. It ensures proper chromosome segregation, spindle assembly, and DNA repair. Loss of FOXM1 impairs proliferation and causes mitotic defects, while overexpression accelerates tumorigenesis. Researchers use FOXM1 antibody to study transcriptional regulation, cell cycle control, and tumor progression.

    Clinically, FOXM1 is strongly associated with cancer. Overexpression occurs in breast, liver, prostate, lung, and brain tumors, correlating with aggressive phenotypes and poor prognosis. FOXM1 promotes tumor growth by enhancing proliferation, metastasis, angiogenesis, and therapy resistance. Targeting FOXM1 is an emerging therapeutic strategy, with inhibitors under development. Beyond oncology, FOXM1 also participates in tissue repair, stem cell biology, and aging processes. NSJ Bioreagents provides FOXM1 antibody for use in oncology, stem cell, and regenerative medicine research.

    Experimentally, FOXM1 antibody is applied in western blotting to detect the ~80i 1/290 kDa protein, in immunohistochemistry to assess tumor expression, and in immunofluorescence microscopy to study nuclear localization. ChIP assays using FOXM1 antibody help identify direct gene targets of this transcription factor.

    UniProt

    Q08050

    Pathways

    Positive Regulation of Response to DNA Damage Stimulus
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