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NK2 Homeobox 5 antibody (AA 82-111)

The Rabbit Polyclonal anti-NK2 Homeobox 5 antibody has been validated for WB. It is suitable to detect NK2 Homeobox 5 in samples from Human and Mouse.
Catalog No. ABIN1538648

Quick Overview for NK2 Homeobox 5 antibody (AA 82-111) (ABIN1538648)

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
  • 29
  • 8
  • 6
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)

Clone

RB36777
  • Binding Specificity

    • 6
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 82-111

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This NKX2-5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 82-111 amino acids from the Central region of human NKX2-5.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    NKX2-5 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Expiry Date

    6 months
  • 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.

    Molecular Weight

    34918

    Gene ID

    1482

    NCBI Accession

    NP_001159647, NP_001159648, NP_004378

    UniProt

    P52952

    Pathways

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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