FOXC1 anticorps (C-Term)
Aperçu rapide pour FOXC1 anticorps (C-Term) (ABIN374336)
Antigène
Voir toutes FOXC1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- C-Term
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Séquence
- RTSGAFVYDC SKF
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Specificité
- This antibody detects FOXC1 / FKHL7 / FREAC3 at C-term.
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Réactivité croisée (Details)
- Species reactivity (tested):Human, Mouse, Zebrafish.
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Purification
- Ammonium Sulphate Precipitation followed by antigen Affinity Chromatography using the immunizing peptide
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Immunogène
- Peptide from C-Terminus of the protein sequence according to NP_001444.2. Genename: FOXC1
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Indications d'application
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Peptide ELISA: Limit dilution 1: 32000. Western blot: 0.5-1.5 μg/mL. Approx 55 kDa band observed in Human Bone Marrow lysates(calculated MW of 56.5 kDa according to NP_001444.1). Immunohistochemistry: 3 μg/mL. In paraffin embedded Human Kidney shows nuclearstaining of some cells in the glomeruli.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. -
Restrictions
- For Research Use only
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Concentration
- 0.5 mg/mL
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Buffer
- Tris saline, pH ~7.3, 0.02 % Sodium Azide, 0.5 % BSA
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Conseil sur la manipulation
- Avoid repeated freezing and thawing.
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Stock
- 4 °C/-20 °C
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Stockage commentaire
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C.
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: "FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost." dans: Investigative ophthalmology & visual science, Vol. 59, Issue 6, pp. 2548-2554, (2019) (PubMed).
: "Foxc1 and Foxc2 deletion causes abnormal lymphangiogenesis and correlates with ERK hyperactivation." dans: The Journal of clinical investigation, Vol. 126, Issue 7, pp. 2437-51, (2017) (PubMed).
: "Dysfunction of the stress-responsive FOXC1 transcription factor contributes to the earlier-onset glaucoma observed in Axenfeld-Rieger syndrome patients." dans: Cell death & disease, Vol. 5, pp. e1069, (2014) (PubMed).
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- FOXC1 (Forkhead Box C1 (FOXC1))
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Autre désignation
- FOXC1 / FKHL7 / FREAC3
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Sujet
- FOXC1 belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined, however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.Synonyms: FREAC-3, Forkhead box protein C1, Forkhead-related protein FKHL7, Forkhead-related transcription factor 3
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Poids moléculaire
- 56.8kDa (NP_001444.1).
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ID gène
- 2296
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NCBI Accession
- NP_001444
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UniProt
- Q12948
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Pathways
- Chromatin Binding, Glycosaminoglycan Metabolic Process
Antigène
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