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HMGB3 antibody

This Mouse Monoclonal antibody specifically detects HMGB3 in WB, IHC (p), IF and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7881047
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for HMGB3 antibody (ABIN7881047)

Target

See all HMGB3 Antibodies
HMGB3 (High Mobility Group Box 3 (HMGB3))

Reactivity

  • 54
  • 29
  • 14
  • 6
  • 6
  • 6
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 50
  • 6
  • 1
Mouse

Clonality

  • 51
  • 6
Monoclonal

Conjugate

  • 40
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HMGB3 antibody is un-conjugated

Application

  • 42
  • 20
  • 13
  • 7
  • 5
  • 5
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF), Flow Cytometry (FACS)

Clone

7G13
  • Purpose

    HMGB3 Antibody / HMG4

    Sequence

    EMAKADKVRY DREMKDYGPA KGGKKKKDPN APKR

    Purification

    Affinity purified

    Immunogen

    Amino acids EMAKADKVRYDREMKDYGPAKGGKKKKDPNAPKR from the human protein were used as the immunogen for the HMGB3 antibody.

    Isotype

    IgG2b
  • Application Notes

    Optimal dilution of the HMGB3 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the HMGB3 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    HMGB3 (High Mobility Group Box 3 (HMGB3))

    Alternative Name

    HMGB3

    Background

    High-mobility group protein B, also known as HMG4, is a protein that in humans is encoded by the HMGB3 gene. This gene encodes a member of a family of proteins containing one or more high mobility group DNA-binding motifs. The encoded protein plays an important role in maintaining stem cell populations, and may be aberrantly expressed in tumor cells. A mutation in this gene was associated with microphthalmia, syndromic 13. There are numerous pseudogenes of this gene on multiple chromosomes. Alternative splicing results in multiple transcript variants.

    UniProt

    O15347
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