兔抗FOXC1 多克隆抗体

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.

Applications:

ELISA, WB

Name of antibody:

FOXC1

Immunogen:

Synthetic peptide of human FOXC1

Full name:

forkhead box C1

Synonyms：

ARA; IGDA; IHG1; FKHL7; IRID1; RIEG3; FREAC3; FREAC-3

SwissProt:

Q12948

ELISA Recommended dilution:

2000-5000

WB Predicted band size:

57 kDa

WB Positive control:

Human normal liver tissue

WB Recommended dilution:

500-2000