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FLT1 antibody

The Mouse Monoclonal anti-FLT1 antibody has been validated for WB and ELISA. It is suitable to detect FLT1 in samples from Human.
Catalog No. ABIN2745579

Quick Overview for FLT1 antibody (ABIN2745579)

Target

See all FLT1 Antibodies
FLT1 (Fms-Related tyrosine Kinase 1 (VEGFR1) (FLT1))

Reactivity

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Human

Host

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Mouse

Clonality

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Monoclonal

Conjugate

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This FLT1 antibody is un-conjugated

Application

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Western Blotting (WB), ELISA

Clone

EWC
  • Specificity

    The antibody will detect native human VEGFR-1/Flt-1 in ELISA experiments and on the surface of different human cell types.

    Cross-Reactivity

    Human

    Purification

    Protein G purified.

    Immunogen

    Recombinant human soluble VEGFR-1.

    Isotype

    IgG1
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Centrifuge vial prior to opening. Reconstitute with sterile water to a concentration of 0.1-1.0 mg/mL.

    Concentration

    Lot specific

    Buffer

    Lyophilized.

    Storage

    4 °C,-20 °C

    Storage Comment

    Short Term Storage: +4°C
    Long Term Storage: -20°C
    Stable for at least 6 months after receipt when stored at -20°C.

    Expiry Date

    6 months
  • Target

    FLT1 (Fms-Related tyrosine Kinase 1 (VEGFR1) (FLT1))

    Alternative Name

    VEGFR-1

    Background

    Recombinant human soluble vascular endothelial growth factor receptor-1 (sVEGFR-1) is the naturally occurring form and is a glycosylated monomeric protein. The biological function of sVEGFR-1 seems to be an endogenous regulator of angiogenesis, binding VEGF with the same affinity as the full-length receptor. VEGFR-1 is a tyrosine-protein kinase that acts as a cell-surface receptor for VEGFA, VEGFB and PGF, and plays an essential role in the development of embryonic vasculature, the regulation of angiogenesis, cell survival, cell migration, macrophage function, chemotaxis and cancer cell invasion. It may play an essential role as a negative regulator of embryonic angiogenesis by inhibiting excessive proliferation of endothelial cells. It can promote endothelial cell proliferation, survival and angiogenesis in adulthood. Its function in promoting cell proliferation seems to be cell-type specific. Promotes PGF-mediated proliferation of endothelial cells, proliferation of some types of cancer cells, but does not promote proliferation of normal fibroblasts (in vitro). It has a very high affinity for VEGFA and relatively low protein kinase activity. It may function as a negative regulator of VEGFA signaling by limiting the amount of free VEGFA and preventing its binding to KDR. Modulates KDR signaling by forming heterodimers with KDR. Ligand binding leads to the activation of several signaling cascades. Activation of phospholipase C-gamma (PLCG) leads to the production of the cellular signaling molecules diacylglycerol and inositol 1,4,5-trisphosphate and the activation of protein kinase C. Mediates phosphorylation of PIK3R1, the regulatory subunit of phosphatidylinositol 3-kinase, leading to activation of phosphatidylinositol kinase and the downstream signaling pathway. Mediates activation of MAPK1/ERK2, MAPK3/ERK1 and the MAP kinase signaling pathway, as well as of the AKT1 signaling pathway. Phosphorylates SRC and YES1 and may also phosphorylate CBL.

    UniProt

    P17948

    Pathways

    RTK Signaling, Signaling Events mediated by VEGFR1 and VEGFR2, VEGFR1 Specific Signals
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