Forkhead Box L1 (FOXL1) (N-Term) antibody

Details for Product No. ABIN182528
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Antigen
Synonyms FKH6, FKHL11, FREAC7, Fkh6, fkh-6, zgc:63595, FOXL1, fkh6, fkhl11, freac7, CG1132, Dmel\\CG1132, Dmfd2, FD2, FoxL1, fd2, Foxl1
Epitope
N-Term
(8), (4), (3), (2), (2), (2), (2), (1), (1), (1), (1), (1)
Reactivity
Dog (Canine), Mouse (Murine), Human
(50), (5), (2), (2)
Host
Rabbit
(31), (16), (4)
Clonality
Polyclonal
Application
Immunohistochemistry (IHC), Western Blotting (WB)
(42), (29), (9), (3), (2), (1)
Pubmed 1 reference available
Catalog no. ABIN182528
Quantity 100 µg
Price
229.00 $   Plus shipping costs $45.00
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Immunogen Synthetic peptide directed towards the N terminal of human FOXL1
Sequence HLFDPRLPALAASPMLYLYGPERPGLPLAFAPAAALAASG RAETPQKPPY
Predicted Reactivity Bovine : 100 %, Dog : 100 %, Horse : 100 %, Human : 100 %, Mouse : 80 %
Characteristics This is a rabbit polyclonal antibody against FOXL1. It was validated on Western Blot and immunohistochemistry.
Purification Protein A purified
Alternative Name FOXL1
Background FOXL1 is a member of the forkhead family. The forkhead domain is a monomeric DNA binding motif that defines a rapidly growing family of eukaryotic transcriptional regulators. Genetic and biochemical data suggest a central role in embryonic development for forkhead proteins.
Molecular Weight 36 kDa
Gene ID 2300
NCBI Accession NM_005250, NP_005241
UniProt Q12952
Research Area Chromatin and Nuclear Signaling, Transcription Factors
Application Notes Optimal working dilutions should be determined experimentally by the investigator.
Comment

Antigen size: 345 AA

Restrictions For Research Use only
Format Lyophilized
Reconstitution Add 100 µL of distilled water.
Concentration 1 mg/mL
Buffer PBS buffer with 2 % sucrose
Handling Advice Avoid repeated freeze-thaw cycles.
Storage -20 °C
Storage Comment For longer periods of storage, store at -20 °C
Supplier Images
anti-Forkhead Box L1 (FOXL1) (N-Term) antibody anti-Forkhead Box L1 (FOXL1) (N-Term) antibody
Background publications Fang, Dagenais, Erickson et al.: "Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome." in: American journal of human genetics, Vol. 67, Issue 6, pp. 1382-8, 2000 (PubMed).

Hosts (31), (16), (4)
Reactivities (50), (5), (2), (2)
Applications (42), (29), (9), (3), (2), (1)
Epitopes (8), (4), (3), (2), (2), (2), (2), (1), (1), (1), (1), (1)
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