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MNX1 antibody

MNX1 Reactivity: Human WB Host: Rabbit Monoclonal unconjugated
Catalog No. ABIN7268684
  • Target See all MNX1 Antibodies
    MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))
    Reactivity
    • 57
    • 31
    • 30
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 63
    Rabbit
    Clonality
    • 63
    Monoclonal
    Conjugate
    • 24
    • 6
    • 6
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This MNX1 antibody is un-conjugated
    Application
    • 47
    • 27
    • 14
    • 5
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purpose
    MNX1/HB9/HLXB9 Rabbit mAb
    Cross-Reactivity
    Human, Mouse
    Characteristics
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthesized peptide derived from human MNX1/MNX1/HB9/HLXB9
    Isotype
    IgG
    Top Product
    Discover our top product MNX1 Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))
    Alternative Name
    MNX1 (MNX1 Products)
    Synonyms
    HB9 antibody, HLXB9 antibody, HOXHB9 antibody, SCRA1 antibody, Hlxb9 antibody, MNR2 antibody, hlxb9 antibody, zgc:112174 antibody, motor neuron and pancreas homeobox 1 antibody, motor neuron homeobox transcription factor antibody, MNX1 antibody, mnx1 antibody, Mnx1 antibody
    Background
    This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009],HB9, HLXB9, HOXHB9, SCRA1,Cell Biology & Developmental Biology,Cell Type Marker,Cell Type Marker_Neuron marker,Epigenetics & Nuclear Signaling,Neural Stem Cells,Neuroscience,Stem Cells,Transcription Factors,MNX1
    Molecular Weight
    41kDa
    Gene ID
    3110
    UniProt
    P50219
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