FOXI1 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)
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- Target See all FOXI1 Proteins
- FOXI1 (Forkhead Box I1 (FOXI1))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 2
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This FOXI1 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human FOXI1 / FKHL10 (transcript variant 2) 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 FOXI1 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
- FOXI1 (Forkhead Box I1 (FOXI1))
- Alternative Name
- Foxi1,fkhl10 (FOXI1 Products)
- Synonyms
- FKH10 Protein, FKHL10 Protein, FREAC-6 Protein, FREAC6 Protein, HFH-3 Protein, HFH3 Protein, 5830401E05Rik Protein, Fkh10 Protein, Hfh3 Protein, cb724 Protein, foo Protein, Xfoxi1a Protein, ema Protein, foxi1a Protein, foxi1e Protein, xema Protein, xfoxi1 Protein, FoxI1e Protein, Xema Protein, fkhl10 Protein, freac6 Protein, hfh3 Protein, FOXI1 Protein, forkhead box I1 Protein, forkhead box i1 Protein, forkhead box I1 L homeolog Protein, forkhead box protein I1 Protein, FOXI1 Protein, Foxi1 Protein, foxi1 Protein, foxi1.L Protein, CC1G_14832 Protein
- Background
- This gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. This gene may play an important role in the development of the cochlea and vestibulum, as well as in embryogenesis. The encoded protein has been found to be required for the transcription of four subunits of a proton pump found in the inner ear, the kidney, and the epididymis. Mutations in this gene have been associated with deafness, autosomal recessive 4.
- Molecular Weight
- 30.6 kDa
- NCBI Accession
- NP_658982
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