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forkhead box C1, Mouse, Clone: 4D11, Abnova™
Mouse monoclonal antibody raised against a full-length recombinant FOXC1.
Supplier: Abnova Corporation H00002296M05
Description
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
Sequence: AAHQGRLTSWYLNQAGGDLGHLASAAAAAAAAGYPGQQQNFHSVREFESQRIGLNNSPVNGNSSCQMAFPSSQSLYRTSGAFVYDCSKF*Specifications
forkhead box C1 | |
Monoclonal | |
Unconjugated | |
PBS with no preservative; pH 7.4 | |
NM_001453 | |
FOXC1 | |
FOXC1 (NP_001444, 464 a.a. ∼ 553 a.a) full length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. | |
100 μg | |
Transcription Regulation | |
Primary | |
Human | |
Antibody |
ELISA, Western Blot | |
4D11 | |
Mouse monoclonal antibody raised against a full length recombinant FOXC1. | |
FOXC1 | |
ARA/FKHL7/FREAC-3/FREAC3/IGDA/IHG1/IRID1 | |
Mouse | |
Affinity Purified | |
RUO | |
Yes | |
2296 | |
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. | |
IgG2b κ |
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