FKBP14 Polyclonal antibody

FKBP14 Polyclonal Antibody for WB, IHC, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, IHC, IF, ELISA

Conjugate

Unconjugated

Cat no : 15884-1-AP

Synonyms

FKBP-22, FKBP22, FKBP-14, FK506-binding protein 14, EC:5.2.1.8



Tested Applications

Positive WB detected inHEK-293 cells, HeLa cells, human brain tissue
Positive IHC detected inhuman ovary cancer tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:2400
Immunohistochemistry (IHC)IHC : 1:50-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

15884-1-AP targets FKBP14 in WB, IHC, IF, ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Cited Reactivityhuman
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen FKBP14 fusion protein Ag8668
Full Name FK506 binding protein 14, 22 kDa
Calculated Molecular Weight 211 aa, 24 kDa
Observed Molecular Weight 28 kDa
GenBank Accession NumberBC005206
Gene Symbol FKBP14
Gene ID (NCBI) 55033
RRIDAB_2102702
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

FKBP14, also named as FKBP22, belongs to the family of FK506-binding peptidyl-prolyl cis-trans isomerases (PPIases). PPIases accelerate the folding of proteins during protein synthesis. FKBP14 is localized in the endoplasmic reticulum (ER) and that deficiency of FKBP14 leads to enlarged ER cisterns in dermal fibroblasts in vivo. FKBP14 is about 22kd.

Protocols

Product Specific Protocols
WB protocol for FKBP14 antibody 15884-1-APDownload protocol
IHC protocol for FKBP14 antibody 15884-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB,IF

Am J Hum Genet

Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss.

Authors - Baumann Matthias M
humanWB,IF

Sci Rep

The novel missense mutation Met48Lys in FKBP22 changes its structure and functions.

Authors - Yoshihiro Ishikawa
humanIF

Hum Mutat

Kyphoscoliotic Ehlers-Danlos syndrome caused by pathogenic variants in FKBP14: Further insights into the phenotypic spectrum and pathogenic mechanisms

Authors - Birute Burnyte
humanWB

Int J Mol Sci

Local Net Charge State of Collagen Triple Helix Is a Determinant of FKBP22 Binding to Collagen III

Authors - Yoshihiro Ishikawa