蛋白
抗体
检测试剂盒
蛋白MARKER
分子生物学
规格：
查看说明书FOXC1 Rabbit pAb
Cat#:DPA03147应用：WB,IHC,ICC/IF,FC,IP
| Product Name: | FOXC1 Rabbit pAb |
| Cat No.: | DPA03147 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human, Mouse |
| Tested Applications: | WB,IHC,ICC/IF,FC,IP |
| Recommended Dilution: | WB: 1:1000 IHC: 1:100 ICC/IF: 1:20 FC: 1:20 IP: 1:20 |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | A synthetic peptide of human FOXC1 |
| Calculated Molecular Weight: | 57 kDa |
| Observed Molecular Weight: | 75 kDa |
| GenBank Accession Number: | Q12948 |
| Gene ID (NCBI): | 2296 |
| Synonyms: | ARA; IGDA; IHG1; ASGD3; FKHL7; IRID1; RIEG3; FREAC3; FREAC-3 |
| 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] |
| Category: | Primary Ab |
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