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RNASEH2B antibody

This Mouse Monoclonal antibody specifically detects RNASEH2B in WB, ICC and IF. It exhibits reactivity toward Human.
Catalog No. ABIN7467894

Quick Overview for RNASEH2B antibody (ABIN7467894)

Target

See all RNASEH2B Antibodies
RNASEH2B (Ribonuclease H2, Subunit B (RNASEH2B))

Reactivity

  • 15
  • 1
  • 1
Human

Host

  • 14
  • 1
Mouse

Clonality

  • 14
  • 1
Monoclonal

Conjugate

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
This RNASEH2B antibody is un-conjugated

Application

  • 15
  • 11
  • 7
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)

Clone

GT479
  • Cross-Reactivity

    Human

    Purification

    Affinity purified by Protein G.

    Immunogen

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

    Isotype

    IgG1
  • Application Notes

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

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1XPBS pH 7, 20 % Glycerol, No Preservative

    Preservative

    Without preservative

    Storage

    4 °C,-20 °C

    Storage Comment

    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.
  • Target

    RNASEH2B (Ribonuclease H2, Subunit B (RNASEH2B))

    Alternative Name

    ribonuclease H2 subunit B

    Background

    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]

    Molecular Weight

    35 kDa

    Gene ID

    79621

    UniProt

    Q5TBB1
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