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GRAF anticorps (AA 584-791)

L’anticorps Lapin Polyclonal anti-GRAF a été validé pour WB et ELISA. Il convient pour détecter GRAF dans des échantillons de Humain, Souris et Rat.
N° du produit ABIN7602088

Aperçu rapide pour GRAF anticorps (AA 584-791) (ABIN7602088)

Antigène

Voir toutes GRAF (ARHGAP26) Anticorps
GRAF (ARHGAP26) (rho GTPase Activating Protein 26 (ARHGAP26))

Reactivité

Humain, Souris, Rat

Hôte

  • 39
  • 3
  • 1
Lapin

Clonalité

  • 40
  • 2
Polyclonal

Conjugué

  • 19
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GRAF est non-conjugé

Application

  • 36
  • 21
  • 20
  • 13
  • 13
  • 5
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Épitope

    • 15
    • 9
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 584-791

    Fonction

    Anti-GRAF/ARHGAP26 Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-GRAF/ARHGAP26 Antibody Picoband® (ABIN7602088). Tested in ELISA, WB applications. This antibody reacts with Human, Mouse, Rat. 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 GRAF/ARHGAP26 recombinant protein (Position: S584-E791).

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    ELISA, 0.1-0.5 μg/mL, -
    1. Borkhardt, A., Bojesen, S., Haas, O. A., Fuchs, U., Bartelheimer, D., Loncarevic, I. F., Bohle, R. M., Harbott, J., Repp, R., Jaeger, U., Viehmann, S., Henn, T., Korth, P., Scharr, D., Lampert, F. The human GRAF gene is fused to MLL in a unique t(5,11)(q31,q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q. Proc. Nat. Acad. Sci. 97: 9168-9173, 2000. 2. Hildebrand, J. D., Taylor, J. M., Parsons, T. J. An SH3 domain-containing GTPase-activating protein for Rho and Cdc42 associates with focal adhesion kinase. Molec. Cell. Biol. 16: 3169-3178, 1996. 3. Ishikawa, K., Nagase, T., Suyama, M., Miyajima, N., Tanaka, A., Kotani, H., Nomura, N., Ohara, O. Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro. DNA Res. 5: 169-176, 1998.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 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, 0.2 mg Na2HPO4.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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 freezing and thawing.
  • Antigène

    GRAF (ARHGAP26) (rho GTPase Activating Protein 26 (ARHGAP26))

    Autre désignation

    ARHGAP26

    Sujet

    Synonyms: BMP and activin membrane-bound inhibitor homolog, Non-metastatic gene A protein, Putative transmembrane protein, NMA, BAMBI, NMA

    Tissue Specificity: Expressed in adult liver.

    Background: Rho GTPase activating protein 26 (ARHGAP26) also known as GTPase Regulator Associated with Focal Adhesion Kinase (GRAF) is a protein that in humans is encoded by the ARHGAP26 gene. Interaction of a cell with the extracellular matrix triggers integrin cell surface receptors to begin signaling cascades that regulate the organization of the actin-cytoskeleton. One of the proteins involved in these cascades is focal adhesion kinase. The protein encoded by this gene is a GTPase activating protein that binds to focal adhesion kinase and mediates the activity of the GTP binding proteins RhoA and Cdc42. Defects in this gene are a cause of juvenile myelomonocytic leukemia (JMML). Multiple transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    100 kDa

    ID gène

    23092
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