ARG57079
anti-FKBP14 antibody [18E2]
anti-FKBP14 antibody [18E2] for Western blot and Human
Overview
| Product Description | Mouse Monoclonal antibody [18E2] recognizes FKBP14 |
|---|---|
| Tested Reactivity | Hu |
| Tested Application | WB |
| Host | Mouse |
| Clonality | Monoclonal |
| Clone | 18E2 |
| Isotype | IgG1, kappa |
| Target Name | FKBP14 |
| Antigen Species | Human |
| Immunogen | Recombinant fragment around aa. 20-211 of Human FKBP14. |
| Conjugation | Un-conjugated |
| Alternate Names | EDSKMH; Rotamase; FKBP-14; FKBP22; FK506-binding protein 14; EC 5.2.1.8; PPIase FKBP14; 22 kDa FKBP; FKBP-22; IPBP12; 22 kDa FK506-binding protein; Peptidyl-prolyl cis-trans isomerase FKBP14 |
Application Instructions
| Application Suggestion |
|
||||
|---|---|---|---|---|---|
| Application Note | * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
| Form | Liquid |
|---|---|
| Purification | Purification with Protein A. |
| Buffer | PBS (pH 7.4), 0.02% Sodium azide and 10% Glycerol. |
| Preservative | 0.02% Sodium azide |
| Stabilizer | 10% Glycerol |
| Concentration | 1 mg/ml |
| Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
| Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
| Database Links |
Swiss-port # Q9NWM8 Human Peptidyl-prolyl cis-trans isomerase FKBP14 |
|---|---|
| Gene Symbol | FKBP14 |
| Gene Full Name | FK506 binding protein 14, 22 kDa |
| Background | The protein encoded by this gene is a member of the FK506-binding protein family of peptidyl-prolyl cis-trans isomerases. The encoded protein is found in the lumen of the endoplasmic reticulum, where it is thought to accelerate protein folding. Defects in this gene are a cause of a type of Ehlers-Danlos syndrome (EDS). Both a protein-coding variant and noncoding variants are transcribed from this gene. [provided by RefSeq, Mar 2012] |
| Function | PPIases accelerate the folding of proteins during protein synthesis. [UniProt] |
| Calculated MW | 24 kDa |
