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The antibody against FKBP10 was raised in rabbit using the Recombinant Human Peptidyl-prolyl cis-trans isomerase FKBP10 protein (459-579AA) as the immunogen. This antibody exists as a fitc conjugated isotype IgG, purified by protein G with a purity greater than 95%.
The antibody against FKBP10 was raised in rabbit using the Recombinant Human Peptidyl-prolyl cis-trans isomerase FKBP10 protein (459-579AA) as the immunogen. This antibody exists as a fitc conjugated isotype IgG, purified by protein G with a purity greater than 95%.
$299.00
| Cat.No | ADC-03938A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | FKBP10 |
| Form | Liquid | Species Reactivity | Human |
| Isotype | IgG | Storage Buffer | 0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4 |
| Purification Method | >95%, Protein G purified | Conjugate | FITC conjugated |
| Storage | Upon receipt |
| Immunogen Description | Recombinant Human Peptidyl-prolyl cis-trans isomerase FKBP10 protein (459-579AA) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | and peptides are available upon request., Complete sequences for the immunogen, target protein | Uniprot ID | Q96AY3 |
Uniprot Id
Q96AY3
Target Species
Human
Target Name
FKBP10
Target Full Name
Peptidyl-prolyl cis-trans isomerase FKBP10
Target Function
PPIases accelerate the folding of proteins during protein synthesis.
Target Involvement
Osteogenesis imperfecta 11 (OI11); Bruck syndrome 1 (BRKS1)
Target Subcellular Location
Endoplasmic reticulum lumen.
Target Synonyms
FKBP10; FKBP65; PSEC0056Peptidyl-prolyl cis-trans isomerase FKBP10; PPIase FKBP10; EC 5.2.1.8; 65 kDa FK506-binding protein; 65 kDa FKBP; FKBP-65; FK506-binding protein 10; FKBP-10; Immunophilin FKBP65; Rotamase
Target Background
The protein encoded by this gene belongs to the FKBP-type peptidyl-prolyl cis/trans isomerase (PPIase) family. This protein localizes to the endoplasmic reticulum and acts as a molecular chaperone. Alternatively spliced variants encoding different isoforms have been reported, but their biological validity has not been determined.
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