MNX1 (NM_005515) Human Recombinant Protein
Product Specifications
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]
Synonyms
HB9; HLXB9; HOXHB9; SCRA1
Gene ID
3110
UniProt
P50219
Accession Number mRNA
NM_005515
Chromosomal Location
7q36.3
Expression System
HEK293T
Tag
C-Myc/DDK
Related Pathways
Maturity onset diabetes of the young
Field of Research
Maturity onset diabetes of the young
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Druggable Genome, ES Cell Differentiation/IPS
Molecular Weight
40.4 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
MNX1
Species
Human
Protein ID
NP_005506
Overview
Recombinant protein of human motor neuron and pancreas homeobox 1 (MNX1)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/3110
Uniprot URL
https://www.uniprot.org/uniprot/P50219
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_005515
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_005506
Curated Selection
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