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Glypican 3 anticorps (AA 32-535)

L’anticorps Lapin Polyclonal anti-Glypican 3 a été validé pour FACS, WB et ELISA. Il convient pour détecter Glypican 3 dans des échantillons de Humain.
N° du produit ABIN7601314

Aperçu rapide pour Glypican 3 anticorps (AA 32-535) (ABIN7601314)

Antigène

Voir toutes Glypican 3 (GPC3) Anticorps
Glypican 3 (GPC3)

Reactivité

  • 175
  • 64
  • 51
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 106
  • 67
  • 5
  • 2
  • 1
  • 1
Lapin

Clonalité

  • 90
  • 84
  • 5
Polyclonal

Conjugué

  • 76
  • 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
  • 1
Cet anticorp Glypican 3 est non-conjugé

Application

  • 97
  • 85
  • 78
  • 60
  • 56
  • 26
  • 21
  • 17
  • 13
  • 7
  • 6
  • 2
  • 1
  • 1
  • 1
Flow Cytometry (FACS), Western Blotting (WB), ELISA
  • Épitope

    • 22
    • 16
    • 12
    • 7
    • 7
    • 6
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 32-535

    Fonction

    Anti-Glypican 3/GPC3 Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    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.

    Purification

    Immunogen affinity purified.

    Immunogène

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

    Isotype

    IgG
  • Indications d'application

    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.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Concentration

    500 μg/mL

    Buffer

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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.
  • Antigène

    Glypican 3 (GPC3)

    Autre désignation

    GPC3

    Sujet

    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.

    Poids moléculaire

    66 kDa

    ID gène

    2719

    UniProt

    P51654

    Pathways

    Glycosaminoglycan Metabolic Process
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