Product nameAnti-FOXF1 antibody
See all FOXF1 primary antibodies
DescriptionRabbit polyclonal to FOXF1
Tested applicationsSuitable for: ICC/IF, IHC-P, WBmore details
Species reactivityReacts with: Human
Predicted to work with: Mouse, Chicken, Cow, Dog, Xenopus laevis
- Fetal placental lysate.
Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Storage bufferPreservative: 0.09% Sodium azide
Constituents: 2% Sucrose, PBS
Concentration information loading...
PurityProtein A purified
Our Abpromise guarantee covers the use of ab23194 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|ICC/IF||Use at an assay dependent concentration. PubMed: 21341990|
|IHC-P||Use at an assay dependent concentration. PubMed: 20722018|
|WB||Use a concentration of 2.5 µg/ml. Detects a band of approximately 38 kDa (predicted molecular weight: 40 kDa). Good results were obtained when blocked with 5% non-fat dry milk in 0.05% PBS-T.|
FunctionProbable transcription activator for a number of lung-specific genes.
Tissue specificityLung and placenta.
Involvement in diseaseDefects in FOXF1 are the cause of alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) [MIM:265380]. ACDMPV is a rare malformation due to abnormal development of the capillary vascular system in the lungs. Histologically, it is characterized by failure of formation and ingrowth of alveolar capillaries, medial muscular thickening of small pulmonary arterioles with muscularization of the intraacinar arterioles, thickened alveolar walls, and anomalously situated pulmonary veins running alongside pulmonary arterioles and sharing the same adventitial sheath. Less common features include a reduced number of alveoli and a patchy distribution of the histopathologic changes. Affected infants present with respiratory distress and the disease is fatal within the newborn period. Additional features include multiple congenital anomalies affecting the cardiovascular, gastrointestinal, genitourinary, and musculoskeletal systems, as well as disruption of the normal right-left asymmetry of intrathoracic or intraabdominal organs. ACDMPV is a rare cause of persistent pulmonary hypertension of the newborn, an abnormal physiologic state caused by failure of transition of the pulmonary circulation from the high pulmonary vascular resistance of the fetus to the low pulmonary vascular resistance of the newborn.
Sequence similaritiesContains 1 fork-head DNA-binding domain.
DomainActivation domains C-terminal of (and distinct from) the forkhead domains are necessary for transcriptional activation.
- Information by UniProt
- AI450827 antibody
- FKH L5 antibody
- FKHL 5 antibody
Anti-FOXF1 antibody (ab23194) at 1.2 µg/ml + Placenta
Predicted band size: 40 kDa
Observed band size: 38 kDa why is the actual band size different from the predicted?
Gel concentration: 12%
ab23194 has been referenced in 5 publications.
- Zhao F et al. Propranolol suppresses HUVEC viability, migration, VEGF expression, and promotes apoptosis by downregulation of miR-4295. J Cell Biochem 120:6614-6623 (2019). PubMed: 30368887
- Acosta SA et al. Endothelial Progenitor Cells Modulate Inflammation-Associated Stroke Vasculome. Stem Cell Rev 15:256-275 (2019). PubMed: 30739275
- Wei HJ et al. FOXF1 mediates mesenchymal stem cell fusion-induced reprogramming of lung cancer cells. Oncotarget 5:9514-29 (2014). WB ; Human . PubMed: 25237908
- Bozyk PD et al. Mesenchymal stromal cells from neonatal tracheal aspirates demonstrate a pattern of lung-specific gene expression. Stem Cells Dev 20:1995-2007 (2011). ICC/IF ; Human . PubMed: 21341990
- Minogue BM et al. Characterization of the human nucleus pulposus cell phenotype and evaluation of novel marker gene expression to define adult stem cell differentiation. Arthritis Rheum 62:3695-705 (2010). IHC-P ; Human . PubMed: 20722018