FOXC1 Antibody

• 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.

• NCBI Gene ID :

  2296

• Swiss Prot :

  Q12948

• Host :

  Rabbit

• Reactivity :

  Human, Mouse, Rat

• Immunogen :

  Recombinant fusion protein containing a sequence corresponding to amino acids 404-553 of human FOXC1 (NP_001444.2) .

• Clonality :

  Polyclonal

• Conjugation :

  Unconjugated

• Type :

  Primary Antibodies

• Field of Research :

  Cell Cycle, Transcription

• Purification :

  Affinity purification

• Positive Control :

  HeLa

• Concentration :

  Batch dependent

• Buffer :

  PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

• Modification :

  None

• Shipping Conditions :

  Blue Ice

• Storage Conditions :

  Store at -20˚ C. Avoid freeze / thaw cycles.

• Calculated Molecular Weight :

  Observed: 70kDa

• Fragment :

  IgG

• Symbol :

  FOXC1

• Positive Control 2 :

  Jurkat

• Positive Control 3 :

  SKOV3

• Positive Control 4 :

  Mouse kidney

• Positive Control 5 :

  Mouse lung

• Positive Control 6 :

  Rat brain

• NCBI Official Name :

  Forkhead box C1

• NCBI Organism :

  Homo sapiens

• Other Product Names :

  FOXC1, ARA, IGDA, IHG1, FKHL7, IRID1, RIEG3, FREAC3, FREAC-3

• Tested Applications :

  WB, IHC

• Physical Properties :

  Liquid