FKBP14 Protein (AA 20-211) (His tag)
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- Target See all FKBP14 Proteins
- FKBP14 (FK506 Binding Protein 14, 22 KDa (FKBP14))
- Protein Type
- Recombinant
- Protein Characteristics
- AA 20-211
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Origin
- Human
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Source
- Escherichia coli (E. coli)
- Purification tag / Conjugate
- This FKBP14 protein is labelled with His tag.
- Application
- SDS-PAGE (SDS)
- Characteristics
- FKBP14, 20-211aa, Human, His tag, E.coli
- Purity
- > 90 % by SDS - PAGE
- Top Product
- Discover our top product FKBP14 Protein
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- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/ml (determined by Bradford assay)
- Buffer
- Liquid in Phosphate-Buffered Saline (pH 7.4) containing 10% glycerol
- Storage
- 4 °C
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- Target
- FKBP14 (FK506 Binding Protein 14, 22 KDa (FKBP14))
- Alternative Name
- FKBP14 (FKBP14 Products)
- Synonyms
- MGC81908 Protein, MGC89927 Protein, BC029109 Protein, FKBP-14 Protein, FKBP22 Protein, EDSKMH Protein, IPBP12 Protein, FK506 binding protein 14 Protein, FK506 binding protein 14 L homeolog Protein, FK506 binding protein 14, 22 kDa Protein, peptidyl-prolyl cis-trans isomerase FKBP14 Protein, FKBP14 Protein, fkbp14.L Protein, fkbp14 Protein, LOC100228355 Protein, Fkbp14 Protein
- Background
- FKBP14, also known as 22 kDa FK506-binding protein, is an enzyme that accelerates the folding of proteins during protein synthesis. This protein contains two EF-hand domains and one PPIase FKBP-type domain. Truncation of the amino-terminus of FKBP14 greatly reduces peptidyl prolyl cis-trans isomerase activity, therefore suggesting that the PPIase FKBP-type domain must be located at the N-terminus. Recombinant human FKBP14 protein, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography. Synonyms: FKBP22, Peptidyl-prolyl cis-trans isomerase FKBP14, 22 kDa FK506 binding protein, FK506 binding protein 14 (22 kDa), FK506 binding protein 14, FKBP 22, FKBP22, Peptidyl prolyl cis trans isomerase, PPIase, Rotamase. NCBI no.: NP_060416
- Molecular Weight
- 24.2 kDa (213aa) confirmed by MALDI-TOF
- Pathways
- ER-Nucleus Signaling
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