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GFI1 anticorps (AA 1-422)

L’anticorps Lapin Polyclonal anti-GFI1 a été validé pour WB, ELISA, IHC et FACS. Il convient pour détecter GFI1 dans des échantillons de Humain, Rat et Souris.
N° du produit ABIN7599380

Aperçu rapide pour GFI1 anticorps (AA 1-422) (ABIN7599380)

Antigène

Voir toutes GFI1 Anticorps
GFI1 (Growth Factor Independent 1 (GFI1))

Reactivité

  • 23
  • 16
  • 15
  • 5
  • 4
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 17
  • 7
Lapin

Clonalité

  • 19
  • 5
Polyclonal

Conjugué

  • 17
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GFI1 est non-conjugé

Application

  • 15
  • 8
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS)
  • Épitope

    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 1-422

    Fonction

    Anti-GFI1 Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-GFI1 Antibody Picoband® (ABIN7599380). Tested in ELISA, Flow Cytometry, IHC, 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 GFI1 recombinant protein (Position: M1-K422).

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    Immunohistochemistry (Paraffin-embedded Section), 0.5-1 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Bell, D. W., Taguchi, T., Jenkins, N. A., Gilbert, D. J., Copeland, N. G., Gilks, C. B., Zweidler-McKay, P., Grimes, H. L., Tsichlis, P. N., Testa, J. R. Chromosomal localization of a gene, GFI1, encoding a novel zinc finger protein reveals a new syntenic region between man and rodents. Cytogenet. Cell Genet. 70: 263-267, 1995. 2. Duan, Z., Horwitz, M. Targets of the transcriptional repressor oncoprotein Gfi-1. Proc. Nat. Acad. Sci. 100: 5932-5937, 2003. Note: Erratum: Proc. Nat. Acad. Sci. 108: 16134 only, 2011. 3. Gilks, C. B., Bear, S. E., Grimes, H. L., Tsichlis, P. N. Progression of interleukin-2 (IL-2)-dependent rat T cell lymphoma lines to IL-2-independent growth following activation of a gene (Gfi1) encoding a novel zinc finger protein. Molec. Cell Biol. 13: 1759-1768, 1993.

    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, 0.2 mg Na2HPO4, 0.05 mg NaN3.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    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

    GFI1 (Growth Factor Independent 1 (GFI1))

    Autre désignation

    GFI1

    Sujet

    Synonyms: Zinc finger protein Gfi-1, Growth factor independent protein 1, Zinc finger protein 163, GFI1, ZNF163

    Tissue Specificity: Isoform 1 is expressed in pancreas. Isoform 2 and isoform 3 is expressed in liver.

    Background: Zinc finger protein Gfi-1 is a transcriptional repressor that in humans is encoded by the GFI1 gene. It is mapped to 1p22.1. This gene encodes a nuclear zinc finger protein that functions as a transcriptional repressor. This protein plays a role in diverse developmental contexts, including hematopoiesis and oncogenesis. It functions as part of a complex along with other cofactors to control histone modifications that lead to silencing of the target gene promoters. Mutations in this gene cause autosomal dominant severe congenital neutropenia, and also dominant nonimmune chronic idiopathic neutropenia of adults, which are heterogeneous hematopoietic disorders that cause predispositions to leukemias and infections. Multiple alternatively spliced variants, encoding the same protein, have been identified for this gene.

    Poids moléculaire

    55 kDa

    ID gène

    2672

    UniProt

    Q99684
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