FKBP14 Antibodies

AND FKBP14 ELISA kits, FKBP14 Proteins

Many biological assays use antibodies to detect FKBP14, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with FKBP14 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop FKBP14 antibodies...

We validate the specificity of these antibodies to FKBP14 by testing them on tissues known to express FKBP14 positively and negatively. Browse below to find the FKBP14 antibody that suites your experiment. We have 3 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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FKBP14 Infographic by Boster Bio

All FKBP14 Products

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Specificity

Applications

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FKBP14 (NM_017946) Human Recombinant Protein

Coomassie blue staining of purified FKBP14 protein

$1249
Cat # PROTQ9NWM8
20 µg

FKBP14 (NM_017946) Human Over-expression Lysate

Human

$628
Cat # LS055033
20 µg, 100 µg

Anti-FKBP14 Antibody Picoband®

Western blot analysis of FKBP14 using anti-FKBP14 antibody (A09867)

Flow Cytometry analysis of HepG2 cells using anti-FKBP14 antibody (A09867)

Human, Mouse, Rat

ELISA, Flow Cytometry, WB

$370
Cat # A09867
100 μg/vial

FKBP14 Overview

Facts about Peptidyl-prolyl cis-trans isomerase FKBP14.

FKBP14 3D structure. Source: alphafold

Peptidyl-prolyl cis-trans isomerase FKBP14 (FKBP14)

PPIase which hastens the folding of proteins during protein synthesis. Has a preference for substrates containing 4- hydroxylproline modifications, including type III collagen.

May also target type VI and type X collagens. .

Gene Information

Human
Gene Name:	FKBP14
Uniprot:	Q9NWM8
Entrez:	55033

Family

Belongs to:

No superfamily

Alternative Names

22 kDa FK506-binding protein; EC 5.2.1.8; FK506 binding protein 14 (22 kDa); FK506 binding protein 14, 22 kDa; FK506-binding protein 14; FKBP-14; FKBP-22; FKBP22PPIase FKBP14; FLJ20731; peptidyl-prolyl cis-trans isomerase FKBP14,22 kDa FKBP; rotamase

Molecular Weight

Mass (kDA):
24.172 kDA

Genomic Context


Human

Location:	7p14.3
Sequence:	7; NC_000007.14 (30010587..30026702, complement)

Subcellular Localizations

Endoplasmic reticulum lumen.

Diseases

Myopathy
Glioblastoma Multiforme
Polymorphic Ventricular Tachycardia
Congenital Muscular Dystrophy (disorder)
Joint Laxity
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 (disorder)
Glioblastoma
Neuromuscular Diseases
Malignant Paraganglionic Neoplasm
Eichsfeld Type Congenital Muscular Dystrophy
Ullrich Congenital Muscular Dystrophy
Ehlers-danlos Syndrome

Dystrophy
Muscle Hypotonia
Scoliosis, Unspecified
Tachycardia, Ventricular
Muscular Dystrophy
Kyphoscoliosis Deformity Of Spine

Pathways

Protein Folding
Excretion

PTMs

Disulfide bond

Glycoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/FKBP14

References

PMID: 22265013 by Baumann M., et al. Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss.

PMID: 24821723 by Ishikawa Y., et al. A substrate preference for the rough endoplasmic reticulum resident protein FKBP22 during collagen biosynthesis.