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NKX2-1 antibody (AA 197-226)

The Rabbit Polyclonal anti-NKX2-1 antibody has been validated for WB. It is suitable to detect NKX2-1 in samples from Human.
Catalog No. ABIN1538042

Quick Overview for NKX2-1 antibody (AA 197-226) (ABIN1538042)

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

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  • 38
Polyclonal

Conjugate

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

Application

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Western Blotting (WB)

Clone

RB37578
  • Binding Specificity

    • 11
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    • 2
    • 1
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    AA 197-226

    Predicted Reactivity

    M, Rat

    Purification

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

    Immunogen

    This NKX2-1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 197-226 amino acids from the Central region of human NKX2-1.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    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

    NKX2-1 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

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

    Alternative Name

    NKX2-1

    Background

    This gene encodes a protein initially identified as a thyroid-specific transcription factor. The encoded protein 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.

    Molecular Weight

    38596

    Gene ID

    7080

    NCBI Accession

    NP_001073136, NP_003308

    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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