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TCF4 antibody (AA 518-667)

This anti-TCF4 antibody is a Mouse Monoclonal antibody detecting TCF4 in ELISA and FACS. Suitable for Human.
Catalog No. ABIN5542393

Quick Overview for TCF4 antibody (AA 518-667) (ABIN5542393)

Target

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

Reactivity

  • 70
  • 19
  • 15
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 52
  • 17
  • 1
Mouse

Clonality

  • 51
  • 19
Monoclonal

Conjugate

  • 36
  • 5
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TCF4 antibody is un-conjugated

Application

  • 57
  • 29
  • 21
  • 13
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
ELISA, Flow Cytometry (FACS)

Clone

7B1B3
  • Binding Specificity

    • 13
    • 10
    • 8
    • 8
    • 7
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 518-667

    Purpose

    TCF4 Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human TCF4 (AA: 518-667) expressed in E. Coli.

    Isotype

    IgG2b
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    TCF4 (Transcription Factor 4 (TCF4))

    Alternative Name

    TCF4

    Background

    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.

    Molecular Weight

    71.3 kDa

    Gene ID

    6925

    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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