ARG63871
anti-FOXC1 antibody
anti-FOXC1 antibody for Western blot and Human
Developmental Biology antibody; Gene Regulation antibody; Chondrogenesis Study antibody
Overview
| Product Description | Goat Polyclonal antibody recognizes FOXC1 |
|---|---|
| Tested Reactivity | Hu |
| Predict Reactivity | Ms, Pig |
| Tested Application | WB |
| Host | Goat |
| Clonality | Polyclonal |
| Isotype | IgG |
| Target Name | FOXC1 |
| Antigen Species | Human |
| Immunogen | C-DAVKDKEEKDRLH |
| Conjugation | Un-conjugated |
| Alternate Names | IRID1; Forkhead box protein C1; FREAC3; IHG1; ARA; IGDA; FREAC-3; Forkhead-related transcription factor 3; RIEG3; FKHL7; Forkhead-related protein FKHL7 |
Application Instructions
| Application Suggestion |
|
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|---|---|---|---|---|---|
| Application Note | WB: Recommend incubate at RT for 1h. * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
| Form | Liquid |
|---|---|
| Purification | Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide. |
| Buffer | Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA |
| Preservative | 0.02% Sodium azide |
| Stabilizer | 0.5% BSA |
| Concentration | 0.5 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 or below. 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 | |
|---|---|
| Background | This gene 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. [provided by RefSeq, Jul 2008] |
| Research Area | Developmental Biology antibody; Gene Regulation antibody; Chondrogenesis Study antibody |
| Calculated MW | 57 kDa |
| PTM | Phosphorylated. |
