FOXC1 antibody (AA 120-200)
Quick Overview for FOXC1 antibody (AA 120-200) (ABIN7220590)
Target
See all FOXC1 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 120-200
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Purpose
- Rabbit Anti-FoxC1/2 Polyclonal Antibody
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Specificity
- 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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Immunogen
- 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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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,IHC 1:100-1:300,IF 1:200-1:1000,ELISA 1:40000,Not yet tested in other applications.
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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
- Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- 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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Expiry Date
- 12 months
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- FOXC1 (Forkhead Box C1 (FOXC1))
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Alternative Name
- FoxC1/2
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Background
- 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.
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Molecular Weight
- 57kD
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Gene ID
- 2296, 2303
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UniProt
- Q12948, Q99958
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Pathways
- Chromatin Binding, Glycosaminoglycan Metabolic Process
Target
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