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NK2 Homeobox 5 antibody (AA 2-5)

This Rabbit Polyclonal antibody specifically detects NK2 Homeobox 5 in WB and ELISA. It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN3032008

Quick Overview for NK2 Homeobox 5 antibody (AA 2-5) (ABIN3032008)

Target

See all NK2 Homeobox 5 (NKX2-5) Antibodies
NK2 Homeobox 5 (NKX2-5)

Reactivity

  • 41
  • 19
  • 7
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 42
  • 8
  • 1
Rabbit

Clonality

  • 44
  • 7
Polyclonal

Conjugate

  • 41
  • 3
  • 2
  • 2
  • 2
  • 1
This NK2 Homeobox 5 antibody is un-conjugated

Application

  • 43
  • 28
  • 8
  • 6
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

    • 7
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2-5

    Purification

    Antigen affinity purified

    Immunogen

    A portion of amino acids 2-5 from the human protein was used as the immunogen for this NKX2.5 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the NKX2.5 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000

    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 NKX2.5 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    NK2 Homeobox 5 (NKX2-5)

    Alternative Name

    NKX2.5

    Background

    This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.

    UniProt

    P52952

    Pathways

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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