FOXC1 anticorps (AA 120-200)
Aperçu rapide pour FOXC1 anticorps (AA 120-200) (ABIN7220590)
Antigène
Voir toutes FOXC1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 120-200
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Fonction
- FoxC1/2 Polyclonal Antibody
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Specificité
- FoxC1/2 Polyclonal Antibody detects endogenous levels of FoxC1/2 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogène
- Synthesized peptide derived from the Internal region of human FoxC1/2 at AA range: 120-200
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Isotype
- IgG
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Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), IF (1:200-1:1000), ELISA (1:40000). Not yet tested in other applications.
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Commentaires
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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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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Stock
- -20 °C
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Stockage commentaire
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- FOXC1 (Forkhead Box C1 (FOXC1))
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Autre désignation
- FoxC1/2
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Sujet
- Rabbit Anti-FoxC1/2 Polyclonal Antibody,FOXC1, FKHL7, FREAC3, Forkhead box protein C1, Forkhead-related protein FKHL7, Forkhead-related transcription factor 3, FREAC-3, FOXC2, FKHL14, MFH1, Forkhead box protein C2, Forkhead-related protein FKHL14, Mesenchyme fork head protein 1,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.,Forkhead box protein C1
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Poids moléculaire
- observerd band 57kDa
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ID gène
- 2296, 2303
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Pathways
- Chromatin Binding, Glycosaminoglycan Metabolic Process
Antigène
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