FOXC1 Antibody
Product Specifications
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
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