FOXL2 recombinant monoclonal antibody, clone 6E10
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More Files
- More Functions
Western Blot
Western blot analysis of Lane 1: human brain cerebral cortex, Lane 2: frontal cortex and Lane 3: cerebellum lysates with FOXL2 recombinant monoclonal antibody, clone 6E10 (Cat # RAB03063).
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Paraffin-embedded sections) of human Alzheimer's disease hippocampus tissue with FOXL2 recombinant monoclonal antibody, clone 6E10 (Cat # RAB03063).
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Specification
Product Description
Rabbit recombinant monoclonal antibody raised against human FOXL2.
Antibody Species
Rabbit
Immunogen
Original antibody is raised against a synthetic peptide corresponding to human FOXL2.
Reactivity
Human
Form
Liquid
Conjugation
Unconjugated
Concentration
batch dependent
Isotype
IgG kappa
Recommend Usage
ELISA
Electron Microscopy
Immunohistochemistry
Immunoprecipitation
Western Blot
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS with 0.02% Proclin 300
Storage Instruction
Store at 4°C for up to 3 months. For longer storage, aliquot and store at -20°C.
Aliquot to avoid repeated freezing and thawing. -
Applications
Western Blot
Western blot analysis of Lane 1: human brain cerebral cortex, Lane 2: frontal cortex and Lane 3: cerebellum lysates with FOXL2 recombinant monoclonal antibody, clone 6E10 (Cat # RAB03063).Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Paraffin-embedded sections) of human Alzheimer's disease hippocampus tissue with FOXL2 recombinant monoclonal antibody, clone 6E10 (Cat # RAB03063).Immunoprecipitation
Enzyme-linked Immunoabsorbent Assay
Electron Microscopy
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Gene Info — FOXL2
Entrez GeneID
668Gene Name
FOXL2
Gene Alias
BPES, BPES1, PFRK, PINTO, POF3
Gene Description
forkhead box L2
Gene Ontology
HyperlinkGene Summary
This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3. [provided by RefSeq
Other Designations
Blepharophimosis, epicanthus inversus, and ptosis 1|blepharophimosis, epicanthus inversus and ptosis|forkhead transcription factor FOXL2
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Interactome
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Disease
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