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NKX2-1 antibody (AA 2-1)

This Rabbit Polyclonal antibody specifically detects NKX2-1 in WB, FACS and ELISA. It exhibits reactivity toward Human.
Catalog No. ABIN3029203

Quick Overview for NKX2-1 antibody (AA 2-1) (ABIN3029203)

Target

See all NKX2-1 Antibodies
NKX2-1 (NK2 Homeobox 1 (NKX2-1))

Reactivity

  • 104
  • 63
  • 63
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 61
  • 44
Rabbit

Clonality

  • 67
  • 38
Polyclonal

Conjugate

  • 53
  • 7
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NKX2-1 antibody is un-conjugated

Application

  • 47
  • 44
  • 35
  • 27
  • 24
  • 23
  • 20
  • 9
  • 7
  • 6
  • 3
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  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS), ELISA
  • Binding Specificity

    • 11
    • 10
    • 6
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2-1

    Cross-Reactivity (Details)

    Expected species reactivity: Mouse, Rat

    Purification

    Antigen affinity purified

    Immunogen

    A portion of amino acids 2-1 from the human protein was used as the immunogen for this TTF1 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the TTF1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,Flow Cytometry: 1:10-1:50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % 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

    -20 °C

    Storage Comment

    Aliquot the TTF1 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    NKX2-1 (NK2 Homeobox 1 (NKX2-1))

    Alternative Name

    NKX2.1 (TTF1)

    Background

    This gene encodes a protein initially identified as a thyroid-specific transcription factor. NKX2.1/TTF1 binds to thyroglobulin promoter and regulates the expression of thyroid-specific genes but has also been shown to regulate the expression of genes involved in morphogenesis. Mutations and deletions in this gene are associated with benign hereditary chorea, choreoathetosis, congenital hypothyroidism, and neonatal respiratory distress, and may be associated with thyroid cancer. Multiple transcript variants encoding different isoforms have been found for this gene.

    UniProt

    P43699

    Pathways

    Intracellular Steroid Hormone Receptor Signaling Pathway, Regulation of Systemic Arterial Blood Pressure by Hormones, Cellular Glucan Metabolic Process, Feeding Behaviour
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