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VEGFA Antikörper (Biotin)

Dieser Anti-VEGFA Antikörper ist ein Human Chimeric Antikörper zur Detektion von VEGFA in FACS. Geeignet für Human.
Produktnummer ABIN7608405

Kurzübersicht für VEGFA Antikörper (Biotin) (ABIN7608405)

Target

Alle VEGFA Antikörper anzeigen
VEGFA (Vascular Endothelial Growth Factor A (VEGFA))

Reaktivität

  • 162
  • 104
  • 78
  • 24
  • 21
  • 19
  • 18
  • 8
  • 6
  • 6
  • 5
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Wirt

  • 190
  • 65
  • 12
  • 2
  • 2
  • 1
Human, Kaninchen

Klonalität

  • 198
  • 73
  • 1
Chimeric

Konjugat

  • 140
  • 40
  • 20
  • 10
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser VEGFA Antikörper ist konjugiert mit Biotin

Applikation

  • 206
  • 91
  • 78
  • 40
  • 40
  • 37
  • 37
  • 26
  • 24
  • 16
  • 14
  • 10
  • 10
  • 10
  • 8
  • 8
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Flow Cytometry (FACS)

Klon

DMC276
  • Verwendungszweck

    Biotinylated Anti-VEGFA antibody(DMC276), IgG1 Chimeric mAb

    Aufreinigung

    Purified from cell culture supernatant by affinity chromatography

    Isotyp

    IgG1
  • Applikationshinweise

    Flow Cyt 1:100

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

    Lagerung

    -20 °C,-80 °C

    Informationen zur Lagerung

    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

    Haltbarkeit

    12 months
  • Target

    VEGFA (Vascular Endothelial Growth Factor A (VEGFA))

    Andere Bezeichnung

    VEGFA

    Hintergrund

    This gene is a member of the PDGF:VEGF growth factor family. It encodes a heparin-binding protein, which exists as a disulfide-linked homodimer. This growth factor induces proliferation and migration of vascular endothelial cells, and is essential for both physiological and pathological angiogenesis. Disruption of this gene in mice resulted in abnormal embryonic blood vessel formation. This gene is upregulated in many known tumors and its expression is correlated with tumor stage and progression. Elevated levels of this protein are found in patients with POEMS syndrome, also known as Crow-Fukase syndrome. Allelic variants of this gene have been associated with microvascular complications of diabetes 1 (MVCD1) and atherosclerosis. Alternatively spliced transcript variants encoding different isoforms have been described. There is also evidence for alternative translation initiation from upstream non-AUG (CUG) codons resulting in additional isoforms. A recent study showed that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism, and that this isoform is antiangiogenic. Expression of some isoforms derived from the AUG start codon is regulated by a small upstream open reading frame, which is located within an internal ribosome entry site.

    UniProt

    P15692

    Pathways

    RTK Signalweg, Glycosaminoglycan Metabolic Process, Regulation of Cell Size, Tube Formation, Signaling Events mediated by VEGFR1 and VEGFR2, Platelet-derived growth Factor Receptor Signaling, VEGFR1 Specific Signals, VEGF Signaling
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