Species ReactivityBovine (Predicted), Dog (Predicted), Human, Rat (Predicted)
Immunogen DescriptionA synthetic peptide consisting of amino acids, RHAAPYSYDCTKY
ConjugateUnconjugated
Purity DescriptionPurified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Product DescriptionGoat anti-Forkhead box protein C2 (FOXC2) Polyclonal Antibody (Unconjugated), suitable for Pep-ELISA, WB, FC.
Application(s)FC, WB, Pep-ELISA
Application DetailsPeptide ELISA (1:4000), Western Blot (2 µg/mL), Flow Cytometry (10 µg/mL). Biosensis recommends optimal dilutions/concentrations should be determined by the end user.
TargetForkhead box protein C2 (FOXC2)
SpecificityReacts with FOXC2 from Human.
Target Host SpeciesHuman
Species ReactivityBovine (Predicted), Dog (Predicted), Human, Rat (Predicted)
Antibody HostGoat
Antibody TypePolyclonal
Antibody IsotypeIgG
ConjugateUnconjugated
Immunogen DescriptionA synthetic peptide consisting of amino acids, RHAAPYSYDCTKY
SequenceRHAAPYSYDCTKY
Purity DescriptionPurified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
FormatLiquid antibody. Supplied at 0.5 mg/mL in Tris saline, 0.02% sodium azide, pH 7.3 with 0.5% bovine serum albumin.
Storage InstructionsUpon receipt, aliquot and store at -20°C long-term. Store at 2-8°C short-term (up to 2 weeks). Minimize freezing and thawing.
Batch NumberPlease see item label.
Expiration Date12 months after date of receipt (unopened vial).
Scientific BackgroundThis 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 may play a role in the development of mesenchymal tissues. [provided by RefSeq, Jul 2008]
A. Western Blot: (2 µg/mL) of nuclear HEK293 (A) and (1 µg/mL) negative control Human Pancreas (B) lysate [RIPA buffer, 35 ug total protein per lane). Detected by chemiluminescence. B. Flow cytometryanalysis: paraformaldehyde fixed HEK293 cells (blue line), permeabilized with 0.5% Triton. Primary incubation 1hr (10 µg/mL) followed by Alexa Fluor 488 secondary antibody (1 µg/mL). IgG control: Unimmunized goat IgG (black line) followed by Alexa Fluor 488 secondary antibody. C. Staining of Human Breast Cancer: (2 µg/mL) staining of paraffin embedded Human Breast Cancer. Steamed antigen retrieval with Tris/EDTA buffer Ph 9, HRP-staining.