MNX1 Protein (Myc-DYKDDDDK Tag)
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- Target See all MNX1 Proteins
- MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This MNX1 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human MNX1 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product MNX1 Protein
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Motor Neuron and Pancreas Homeobox 1 (MNX1) (AA 1-401) protein (Strep Tag)
Crystallography grade MNX1 Origin: Human Host: Tobacco (Nicotiana tabacum) Recombinant >80 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. ELISA, SDS, WB
Motor Neuron and Pancreas Homeobox 1 (MNX1) (AA 1-404) protein (Strep Tag)Crystallography grade MNX1 Origin: Mouse Host: Tobacco (Nicotiana tabacum) Recombinant ≥ 80 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. ELISA, SDS, WB
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Target
- MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))
- Alternative Name
- Mnx1 (MNX1 Products)
- Synonyms
- HB9 Protein, HLXB9 Protein, HOXHB9 Protein, SCRA1 Protein, Hlxb9 Protein, MNR2 Protein, hlxb9 Protein, zgc:112174 Protein, motor neuron and pancreas homeobox 1 Protein, motor neuron homeobox transcription factor Protein, MNX1 Protein, mnx1 Protein, Mnx1 Protein
- 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.
- Molecular Weight
- 40.4 kDa
- NCBI Accession
- NP_005506
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