FOXC1 Rabbit pAb
Sizes: 20µl, 100µl
Catalogue Numbers: A2924-20, A2924-100
Citations, Manuals and SDS Available upon request.
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.
Synonyms: ARA; IGDA; IHG1; ASGD3; FKHL7; IRID1; RIEG3; FREAC3; FREAC-3; FOXC1
GeneID: 2296
Swiss-Prot: Q12948
Reactivity: Human, Mouse, Rat
Calculated Molecular Weight: 57kDa
Observed Molecular Weight: 70kDa
Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 404-553 of human FOXC1 (NP_001444.2).
Immunogen Species: Human
Host: Rabbit
Isotype: IgG
Purity: Affinity purification
Tested Applications: ELISA, WB
Storage Buffer: Store at -20℃. Avoid freeze / thaw cycles. | Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Recommended Dilutions: WB: 1:100 - 1:1000
Research Areas: Epigenetics Nuclear Signaling, Transcription Factors, Cell Biology Developmental Biology
Modifications: Unmodified
Conjugate: Unconjugated
Positive Samples: HeLa, Jurkat, SKOV3, Mouse kidney, Mouse lung, Rat brain
Cellular Location: Nucleus
Category: Polyclonal Antibodies
Citations, Manuals and SDS Available upon request.