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Glypican 3 Antikörper (AA 32-535)

Der Kaninchen Polyklonal Anti-Glypican 3-Antikörper wurde für FACS, WB und ELISA validiert. Er ist geeignet, Glypican 3 in Proben von Human zu detektieren.
Produktnummer ABIN7601314

Kurzübersicht für Glypican 3 Antikörper (AA 32-535) (ABIN7601314)

Target

Alle Glypican 3 (GPC3) Antikörper anzeigen
Glypican 3 (GPC3)

Reaktivität

  • 184
  • 64
  • 50
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 110
  • 73
  • 5
  • 2
  • 1
  • 1
Kaninchen

Klonalität

  • 97
  • 87
  • 5
Polyklonal

Konjugat

  • 87
  • 15
  • 7
  • 7
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Glypican 3 Antikörper ist unkonjugiert

Applikation

  • 96
  • 86
  • 85
  • 69
  • 57
  • 30
  • 26
  • 18
  • 15
  • 15
  • 6
  • 2
  • 2
  • 1
  • 1
Flow Cytometry (FACS), Western Blotting (WB), ELISA
  • Bindungsspezifität

    • 22
    • 16
    • 12
    • 8
    • 7
    • 7
    • 6
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 32-535

    Verwendungszweck

    Anti-Glypican 3/GPC3 Antibody Picoband®

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-Glypican 3/GPC3 Antibody Picoband® (ABIN7601314). Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Aufreinigung

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human Glypican 3/GPC3 recombinant protein (Position: D32-A535).

    Isotyp

    IgG
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells
    ELISA, 0.1-0.5 μg/mL
    1. Capurro, M. I., Xu, P., Shi, W., Li, F., Jia, A., Filmus, J. Glypican-3 inhibits Hedgehog signaling during development by competing with Patched for Hedgehog binding. Dev. Cell 14: 700-711, 2008. 2. Filmus, J., Capurro, M., Rast, J. Glypicans Genome Biol. 9: 224, 2008. Note: Electronic Article. 3. Filmus, J., Church, J. G., Buick, R. N. Isolation of a cDNA corresponding to a developmentally regulated transcript in rat intestine. Molec. Cell Biol. 8: 4243-4249, 1988.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

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

    Konzentration

    500 μg/mL

    Buffer

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
  • Target

    Glypican 3 (GPC3)

    Andere Bezeichnung

    GPC3

    Hintergrund

    Synonyms: Glypican-3, GTR2-2, Intestinal protein OCI-5, MXR7, Glypican-3 alpha subunit, Glypican-3 beta subunit, GPC3, OCI5

    Tissue Specificity: Highly expressed in lung, liver and kidney.

    Background: Glypican-3 is a protein that, in humans, is encoded by the GPC3 gene. It is mapped to Xq26.2. Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants.

    Molekulargewicht

    66 kDa

    Gen-ID

    2719

    UniProt

    P51654

    Pathways

    Glycosaminoglycan Metabolic Process
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