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TCF4 antibody (AA 147-176)

The Rabbit Polyclonal anti-TCF4 antibody is suitable to detect TCF4 in samples from Human, Mouse and Rat. It has been validated for WB and ELISA.
Catalog No. ABIN7870740
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for TCF4 antibody (AA 147-176) (ABIN7870740)

Target

See all TCF4 Antibodies
TCF4 (Transcription Factor 4 (TCF4))

Reactivity

  • 81
  • 19
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  • 4
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  • 3
  • 2
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 54
  • 26
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Rabbit

Clonality

  • 43
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Polyclonal

Conjugate

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  • 2
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  • 2
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  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TCF4 antibody is un-conjugated

Application

  • 63
  • 35
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  • 9
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  • 3
  • 1
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

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    AA 147-176

    Purpose

    TCF4 Antibody / Transcription factor 4

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids Q147-V176) was used as the immunogen for the TCF4 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the TCF4 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 TCF4 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

    TCF4 (Transcription Factor 4 (TCF4))

    Alternative Name

    TCF4

    Background

    Transcription factor 4 (TCF-4) also known as immunoglobulin transcription factor 2 (ITF-2) is a protein that in humans is encoded by the TCF4 gene located on chromosome 18q21.2. This gene encodes transcription factor 4, a basic helix-loop-helix transcription factor. The encoded protein recognizes an Ephrussi-box ('E-box') binding site ('CANNTG') - a motif first identified in immunoglobulin enhancers. This gene is broadly expressed, and may play an important role in nervous system development. Defects in this gene are a cause of Pitt-Hopkins syndrome. In addition, an intronic CTG repeat normally numbering 10-37 repeat units can expand to >50 repeat units and cause Fuchs endothelial corneal dystrophy. Multiple alternatively spliced transcript variants that encode different proteins have been described.

    UniProt

    P15884

    Pathways

    WNT Signaling, Positive Regulation of Peptide Hormone Secretion, Peptide Hormone Metabolism, Regulation of Hormone Metabolic Process, Carbohydrate Homeostasis, Stem Cell Maintenance, Protein targeting to Nucleus
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