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antibody from antibodies-online
Targeting: FOXG1
BF1, FKH2, FKHL1, FKHL2, FKHL3, FKHL4, FOXG1A, FOXG1B, FOXG1C, HBF-3, HFK1, HFK2, HFK3, QIN
Western blot
ELISAAntibody data
- Antibody Data
- Antigen structure
- References [5]
- Comments [0]
- Validations
- Western blot [1]
- Flow cytometry [1]
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- Product number
- ABIN952368 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Forkhead Box G1 (FOXG1) (AA 231-261), (Middle Region) antibody
- Antibody type
- Polyclonal
- Antigen
- KLH conjugated synthetic peptide between 231~261 amino acids from the Central region of human FOXG1.
- Description
- Protein A column, followed by peptide affinity purification
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Epitope
- AA 231-261,Middle Region
- Vial size
- 0.4 mL
- Concentration
- 0.25 mg/mL
- Storage
- Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females.
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.
FOXG1 is responsible for the congenital variant of Rett syndrome.
FOXG1 dysregulation is a frequent event in medulloblastoma.
Comparative evolutionary analysis of the FoxG1 transcription factor from diverse vertebrates identifies conserved recognition sites for microRNA regulation.
Philippe C, Amsallem D, Francannet C, Lambert L, Saunier A, Verneau F, Jonveaux P
Journal of medical genetics 2010 Jan;47(1):59-65
Journal of medical genetics 2010 Jan;47(1):59-65
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.
Mencarelli MA, Spanhol-Rosseto A, Artuso R, Rondinella D, De Filippis R, Bahi-Buisson N, Nectoux J, Rubinsztajn R, Bienvenu T, Moncla A, Chabrol B, Villard L, Krumina Z, Armstrong J, Roche A, Pineda M, Gak E, Mari F, Ariani F, Renieri A
Journal of medical genetics 2010 Jan;47(1):49-53
Journal of medical genetics 2010 Jan;47(1):49-53
FOXG1 is responsible for the congenital variant of Rett syndrome.
Ariani F, Hayek G, Rondinella D, Artuso R, Mencarelli MA, Spanhol-Rosseto A, Pollazzon M, Buoni S, Spiga O, Ricciardi S, Meloni I, Longo I, Mari F, Broccoli V, Zappella M, Renieri A
American journal of human genetics 2008 Jul;83(1):89-93
American journal of human genetics 2008 Jul;83(1):89-93
FOXG1 dysregulation is a frequent event in medulloblastoma.
Adesina AM, Nguyen Y, Mehta V, Takei H, Stangeby P, Crabtree S, Chintagumpala M, Gumerlock MK
Journal of neuro-oncology 2007 Nov;85(2):111-22
Journal of neuro-oncology 2007 Nov;85(2):111-22
Comparative evolutionary analysis of the FoxG1 transcription factor from diverse vertebrates identifies conserved recognition sites for microRNA regulation.
Bredenkamp N, Seoighe C, Illing N
Development genes and evolution 2007 Mar;217(3):227-33
Development genes and evolution 2007 Mar;217(3):227-33
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Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- Western blot analysis of FOXG1 Antibody (Center) Cat.-No AP51708PU-N in mouse brain tissue lysates (35ug/lane). FOXG1 (arrow) was detected using the purified Pab.
Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- Flow cytometric analysis of U251 cells using FOXG1 Antibody (Center) Cat.-No AP51708PU-N (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
