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MNX1 antibody (AA 300-350)

The Rabbit Polyclonal anti-MNX1 antibody is suitable to detect MNX1 in samples from Human. It has been validated for WB and IP.
Catalog No. ABIN7450328
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$457.43
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Quick Overview for MNX1 antibody (AA 300-350) (ABIN7450328)

Target

See all MNX1 Antibodies
MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))

Reactivity

  • 66
  • 41
  • 31
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 71
Rabbit

Clonality

  • 58
  • 13
Polyclonal

Conjugate

  • 27
  • 6
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MNX1 antibody is un-conjugated

Application

  • 56
  • 24
  • 15
  • 14
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP)
  • Binding Specificity

    • 16
    • 8
    • 5
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 300-350

    Purpose

    Rabbit anti-HLXB9 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 300 and 350

    Isotype

    IgG
  • Application Notes

    IP: 2 - 10 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 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

    4 °C

    Expiry Date

    12 months
  • Target

    MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))

    Alternative Name

    HLXB9

    Background

    Background: Homeobox protein HB9 (HLXB9) contains one homeobox DNA-binding domain. HLBX9 is encoded by the motor neuron and pancreas homeobox protein 1 (MNX1) gene. Mutations in MNX1 are the cause of Currarino syndrome and result in presacral tumor, sacral agenesis, and anorectal malformation.

    Gene ID

    3110

    NCBI Accession

    NP_005506

    UniProt

    P50219
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