Full Product Name
MNX1 Antibody (Center)
Product Synonym Names
Motor neuron and pancreas homeobox protein 1; Homeobox protein HB9; MNX1; HLXB9
Product Gene Name
anti-MNX1 antibody
[Similar Products]
Antibody/Peptide Pairs
MNX1 peptide (MBS9221746) is used for blocking the activity of MNX1 antibody (MBS9200892)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Immunogen Sequence Positions
242-271
3D Structure
ModBase 3D Structure for P50219
Species Reactivity
Human, mouse
Specificity
This MNX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 242-271 amino acids from the Central region of human MNX1.
Purity/Purification
Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)
Form/Format
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
Concentration
Vial Concentration: 0.5 (lot specific)
Antigen Type
Synthetic Peptide
Preparation and Storage
Maintain refrigerated at 2-8 degree C for up to 6 months. For long term storage store at -20 degree C in small aliquots to prevent freeze-thaw cycles.
Other Notes
Small volumes of anti-MNX1 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-MNX1 antibody
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].
Product Categories/Family for anti-MNX1 antibody
Developmental Biology; Neuroscience; Signal Transduction
Applications Tested/Suitable for anti-MNX1 antibody
Western Blot (WB), ELISA (EIA)
Application Notes for anti-MNX1 antibody
WB~~1:1000
Western Blot (WB) of anti-MNX1 antibody
MNX1 Antibody (Center) western blot analysis in mouse liver tissue lysates (35ug/lane).This demonstrates the MNX1 antibody detected the MNX1 protein (arrow).

NCBI/Uniprot data below describe general gene information for MNX1. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001158727.1
[Other Products]
NCBI Related Accession #
Human, mouseNP_005506.3[Other Products]
NCBI GenBank Nucleotide #
NM_001165255.1
[Other Products]
UniProt Primary Accession #
P50219
[Other Products]
UniProt Secondary Accession #
Q9Y648; F5H401[Other Products]
UniProt Related Accession #
P50219[Other Products]
NCBI Official Full Name
motor neuron and pancreas homeobox protein 1 isoform 2
NCBI Official Synonym Full Names
motor neuron and pancreas homeobox 1
NCBI Official Symbol
MNX1??[Similar Products]
NCBI Official Synonym Symbols
HB9; HLXB9; SCRA1; HOXHB9
??[Similar Products]
NCBI Protein Information
motor neuron and pancreas homeobox protein 1
UniProt Protein Name
Motor neuron and pancreas homeobox protein 1
UniProt Synonym Protein Names
Homeobox protein HB9
Protein Family
Motor neuron and pancreas homeobox protein
UniProt Gene Name
MNX1??[Similar Products]
UniProt Synonym Gene Names
HLXB9??[Similar Products]
UniProt Entry Name
MNX1_HUMAN
NCBI Summary for MNX1
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]
UniProt Comments for MNX1
MNX1: Putative transcription factor involved in pancreas development and function. Defects in MNX1 are a cause of Currarino syndrome (CURRAS). The triad of a presacral tumor, sacral agenesis and anorectal malformation constitutes the Currarino syndrome which is caused by dorsal-ventral patterning defects during embryonic development. The syndrome occurs in the majority of patients as an autosomal dominant trait.
Protein type: DNA-binding
Chromosomal Location of Human Ortholog: 7q36
Cellular Component: nucleus
Molecular Function: sequence-specific DNA binding; transcription factor activity
Biological Process: regulation of transcription from RNA polymerase II promoter; anatomical structure morphogenesis; transcription, DNA-dependent; spinal cord motor neuron cell fate specification; neuron migration; nerve development; motor axon guidance; endocrine pancreas development; humoral immune response; dorsoventral neural tube patterning; post-embryonic development
Disease: Currarino Syndrome
Product References and Citations for anti-MNX1 antibody
Turgut, M. Acta Neurochir (Wien) 152(6):1083-1084(2010)
Garcia-Barcelo, M.M., et al. J. Pediatr. Surg. 44(10):1892-1898(2009)
Park, J., et al. Cancer Genet. Cytogenet. 191(2):102-105(2009)
Ballabio, E., et al. Leukemia 23(6):1179-1182(2009)
Taketani, T., et al. Cancer Genet. Cytogenet. 186(2):115-119(2008)
Research Articles on MNX1
1. study reports the results of MNX1 mutational screening in a series of 28 cases suspected having Currarino Syndrome and characterization of 10 novel mutations
Precautions
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