IFITM5 Protein (Myc-DYKDDDDK Tag)
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- Target See all IFITM5 Proteins
- IFITM5 (Interferon Induced Transmembrane Protein 5 (IFITM5))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This IFITM5 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human IFITM5 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 IFITM5 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
- IFITM5 (Interferon Induced Transmembrane Protein 5 (IFITM5))
- Abstract
- IFITM5 Products
- Synonyms
- BRIL Protein, DSPA1 Protein, Hrmp1 Protein, OI5 Protein, fragilis4 Protein, 1110003J06Rik Protein, AW213665 Protein, Bril Protein, Hrtm1 Protein, interferon induced transmembrane protein 5 Protein, interferon-induced transmembrane protein 1 Protein, Ifitm5 Protein, IFITM5 Protein, LOC606890 Protein
- Background
- This gene encodes a membrane protein thought to play a role in bone mineralization. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195).
- Molecular Weight
- 14.2 kDa
- NCBI Accession
- NP_001020466
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