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BCL7B antibody (AbBy Fluor® 488)

This Rabbit Polyclonal antibody specifically detects BCL7B in WB and IF (p). It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN1401910

Quick Overview for BCL7B antibody (AbBy Fluor® 488) (ABIN1401910)

Target

See all BCL7B Antibodies
BCL7B (B-Cell CLL/lymphoma 7B (BCL7B))

Reactivity

Human, Mouse, Rat

Host

  • 28
  • 3
Rabbit

Clonality

  • 29
  • 2
Polyclonal

Conjugate

  • 13
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This BCL7B antibody is conjugated to AbBy Fluor® 488

Application

  • 30
  • 13
  • 12
  • 11
  • 5
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Cross-Reactivity

    Human, Mouse, Rat

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human BCL7B

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    BCL7B (B-Cell CLL/lymphoma 7B (BCL7B))

    Alternative Name

    BCL7B

    Background

    Synonyms: B cell CLL/lymphoma 7 protein family member B, B cell CLL/lymphoma 7B, BCL 7B, BCL7B_HUMAN.

    Background: BCL7B shows high homology to the BCL7A protein, which is known to be directly involved in a complex chromosomal translocation in Burkitt lymphoma cell lines. The specific function of BCL7B has not yet been determined. However, it may play a role in lung tumor development or progression. The BCL7B gene is located at a chromosomal region commonly deleted in the congenital disorder, Williams syndrome.

    Gene ID

    9275
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