GTX25079
FOXC1 antibody, C-term
Cannot supply to this region.
- SKU:
- GTX25079
- Additional Names:
- forkhead box C1 , ARA , ASGD3 , FKHL7 , FREAC-3 , FREAC3 , IGDA , IHG1 , IRID1 , RIEG3
- Application:
- Flow Cytometry, WB, IHC-P
- Concentration:
- 0.50 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Ammonium Sulfate Precipitated; Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Goat
- Reactivities:
- Human
- Buffer:
- TBS, 0.5% BSA, 0.02% Sodium azide.
- Immunogen:
- Peptide with sequence RTSGAFVYDCSKF, from the C Terminus of the protein sequence according to NP_001444.2.
- Uniprot:
- Q12948
- Synonyms:
- ARA;ASGD3;FKHL7;forkhead box C1 protein;forkhead box protein C1;forkhead-related activator 3;forkhead-related protein FKHL7;forkhead-related transcription factor 3;forkhead, drosophila, homolog-like 7;forkhead/winged helix-like transcription factor 7;FREAC-3;FREAC3;IGDA;IHG1;IRID1;myeloid factor-delta;RIEG3
- Extra Details:
- 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]
- Shipping Conditions:
- Blue Ice