OLIG2 Protein (Myc-DYKDDDDK Tag)
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- Target See all OLIG2 Proteins
- OLIG2 (Oligodendrocyte Lineage Transcription Factor 2 (OLIG2))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This OLIG2 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human OLIG2 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 OLIG2 Protein
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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
- OLIG2 (Oligodendrocyte Lineage Transcription Factor 2 (OLIG2))
- Alternative Name
- Olig2 (OLIG2 Products)
- Synonyms
- olig3.2 Protein, MGC89336 Protein, OLIG2 Protein, BHLHB1 Protein, OLIGO2 Protein, PRKCBP2 Protein, RACK17 Protein, bHLHe19 Protein, wu:fc64g09 Protein, AI604895 Protein, Bhlhb1 Protein, Olg-2 Protein, Oligo2 Protein, RK17 Protein, oligodendrocyte transcription factor 4 Protein, oligodendrocyte transcription factor 2 Protein, oligodendrocyte lineage transcription factor 2 Protein, olig4 Protein, OLIG2 Protein, Olig2 Protein, olig2 Protein
- Background
- This gene encodes a basic helix-loop-helix transcription factor which is expressed in oligodendroglial tumors of the brain. The protein is an essential regulator of ventral neuroectodermal progenitor cell fate. The gene is involved in a chromosomal translocation t(1421)(q11.2q22) associated with T-cell acute lymphoblastic leukemia. Its chromosomal location is within a region of chromosome 21 which has been suggested to play a role in learning deficits associated with Down syndrome.
- Molecular Weight
- 32.2 kDa
- NCBI Accession
- NP_005797
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