ARG63341

anti-FOXC1 antibody

anti-FOXC1 antibody for Flow cytometry,ICC/IF,IHC-Formalin-fixed paraffin-embedded sections and Human

Developmental Biology antibody; Gene Regulation antibody; Chondrogenesis Study antibody

Overview

Product Description Goat Polyclonal antibody recognizes FOXC1
Tested Reactivity Hu
Predict Reactivity Ms, Rat
Tested Application FACS, ICC/IF, IHC-P
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name FOXC1
Antigen Species Human
Immunogen RTSGAFVYDCSKF
Conjugation Un-conjugated
Alternate Names IRID1; Forkhead box protein C1; FREAC3; IHG1; ARA; IGDA; FREAC-3; Forkhead-related transcription factor 3; RIEG3; FKHL7; Forkhead-related protein FKHL7

Application Instructions

Application Suggestion
Tested Application Dilution
FACS10 µg/ml
ICC/IF10 µg/ml
IHC-PAssay - dependent
Application Note IHC-P: Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0).
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Buffer Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA
Preservative 0.02% Sodium azide
Stabilizer 0.5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 2296 Human FOXC1

Swiss-port # Q12948 Human Forkhead box protein C1

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. [provided by RefSeq, Jul 2008]
Highlight Related Antibody Duos and Panels:
ARG30314 Chondrogenesis Marker Antibody Panel
Related products:
FOXC1 antibodies; FOXC1 Duos / Panels; Anti-Goat IgG secondary antibodies;
Research Area Developmental Biology antibody; Gene Regulation antibody; Chondrogenesis Study antibody
Calculated MW 57 kDa
PTM Phosphorylated.