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Septin 9 anticorps

Cet anticorps anti-Septin 9 est un anticorps Lapin Polyclonal détectant Septin 9 dans WB. Adapté pour Humain.
N° du produit ABIN7467359

Aperçu rapide pour Septin 9 anticorps (ABIN7467359)

Antigène

Voir toutes Septin 9 (SEPT9) Anticorps
Septin 9 (SEPT9)

Reactivité

  • 29
  • 8
  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 25
  • 4
Lapin

Clonalité

  • 28
  • 1
Polyclonal

Conjugué

  • 22
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Septin 9 est non-conjugé

Application

  • 17
  • 11
  • 8
  • 6
  • 5
  • 5
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  •  Réactivité croisée

    Humain, Souris

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Recombinant protein encompassing a sequence within the center region of human SEPT9. The exact sequence is proprietary.

    Isotype

    IgG
  • Indications d'application

    WB: 1:1000-1:10000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Commentaires

    Positive Control: Raji , Mouse liver

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.03 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Antigène

    Septin 9 (SEPT9)

    Autre désignation

    septin 9

    Sujet

    Septin 9 , AF17q25 , MSF , MSF1 , NAPB , PNUTL4 , SINT1 , SeptD1,This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.

    Poids moléculaire

    65 kDa

    ID gène

    10801

    UniProt

    Q9UHD8
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