FKBP14 Antibody Summary
Immunogen |
FKBP14 (NP_060416.1, 1 a.a. - 211 a.a.) full-length human protein. MRLFLWNAVLTLFVTSLIGALIPEPEVKIEVLQKPFICHRKTKGGDLMLVHYEGYLEKDGSLFHSTHKHNNGQPIWFTLGILEALKGWDQGLKGMCVGEKRKLIIPPALGYGKEGKGKIPPESTLIFNIDLLEIRNGPRSHESFQEMDLNDDWKLSKDEVKAYLKKEFEKHGAVVNESHHDALVEDIFDKEDEDKDGFISAREFTYKHDEL |
Specificity |
FKBP14 - FK506 binding protein 14, 22 kDa, |
Isotype |
IgG |
Clonality |
Polyclonal |
Host |
Mouse |
Gene |
FKBP14 |
Purity |
Protein A purified |
Innovator's Reward |
Test in a species/application not listed above to receive a full credit towards a future purchase. |
Applications/Dilutions
Dilutions |
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Application Notes |
Antibody reactive against Recombinant Protein with GST tag on ELISA and Western Blot and also on transfected lysate in western blot. GST tag alone is used as a negative control. |
Publications |
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Packaging, Storage & Formulations
Storage |
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles. |
Buffer |
PBS (pH 7.4) |
Preservative |
No Preservative |
Purity |
Protein A purified |
Notes
This product is produced by and distributed for Abnova, a company based in Taiwan.
Alternate Names for FKBP14 Antibody
Background
PPIases accelerate the folding of proteins during protein synthesis
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are
guaranteed for 1 year from date of receipt.
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Publications for FKBP14 Antibody (H00055033-B01P)(3)
Showing Publications 1 -
3 of 3.
Publications using H00055033-B01P |
Applications |
Species |
Marlies C, Robin V, Tibbe D et al. Kyphoscoliotic Ehlers-Danlos syndrome caused by pathogenic variants in FKBP14: further insights into the phenotypic spectrum and pathogenic mechanisms. Hum Mutat. 2022-09-02 [PMID: 36054293] |
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N Chiarelli, G Carini, N Zoppi, M Ritelli, M Colombi Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome PLoS ONE, 2018-01-18;13(1):e0191220. 2018-01-18 [PMID: 29346445] |
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Baumann M, Giunta C, Krabichler B et al. Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss. Am J Hum Genet. 2012-01-19 [PMID: 22265013] |
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Product General Protocols
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Secondary Antibodies
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