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RNASEH2B anticorps

L’anticorps Souris Monoclonal anti-RNASEH2B a été validé pour WB. Il convient pour détecter RNASEH2B dans des échantillons de Humain.
N° du produit ABIN7464457

Aperçu rapide pour RNASEH2B anticorps (ABIN7464457)

Antigène

Voir toutes RNASEH2B Anticorps
RNASEH2B (Ribonuclease H2, Subunit B (RNASEH2B))

Reactivité

  • 16
  • 1
  • 1
Humain

Hôte

  • 15
  • 1
Souris

Clonalité

  • 14
  • 2
Monoclonal

Conjugué

  • 11
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp RNASEH2B est non-conjugé

Application

  • 16
  • 11
  • 8
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB)

Clone

GT673
  •  Réactivité croisée

    Humain

    Purification

    Affinity purified by Protein G.

    Immunogène

    Recombinant protein encompassing a sequence within the center region of human RNaseH2B. The exact sequence is proprietary.

    Isotype

    IgG1
  • Indications d'application

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Commentaires

    Positive Control: HeLa , HeLa nuclear extract

    Validation: Orthogonal

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    2.01 mg/mL

    Buffer

    PBS, No Preservative

    Agent conservateur

    Without preservative

    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

    RNASEH2B (Ribonuclease H2, Subunit B (RNASEH2B))

    Autre désignation

    ribonuclease H2 subunit B

    Sujet

    Ribonuclease H2 subunit B , AGS2 , DLEU8,RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic subunits (B and C) and specifically degrades the RNA of RNA:DNA hybrids. The protein encoded by this gene is the non-catalytic B subunit of RNase H2, which is thought to play a role in DNA replication. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Aicardi-Goutieres syndrome type 2 (AGS2). [provided by RefSeq]

    Poids moléculaire

    35 kDa

    ID gène

    79621

    UniProt

    Q5TBB1
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