Antibody data
- Antibody Data
- Antigen structure
- References [4]
- Comments [0]
- Validations
- Western blot [2]
- Immunohistochemistry [3]
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- Product number
- ABIN249942 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Forkhead Box C2 (MFH-1, Mesenchyme Forkhead 1) (FOXC2) (C-Term) antibody
- Antibody type
- Polyclonal
- Description
- Immunogen affinity purified
- Reactivity
- Human, Mouse
- Host
- Goat
- Epitope
- C-Term
- Vial size
- 0.1 mg
- Storage
- Store at -20°C. Avoid freeze-thaw cycles.
- Handling
- Avoid freeze-thaw cycles
Submitted references Foxc1 is required by pericytes during fetal brain angiogenesis.
Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development.
Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome.
Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.
Siegenthaler JA, Choe Y, Patterson KP, Hsieh I, Li D, Jaminet SC, Daneman R, Kume T, Huang EJ, Pleasure SJ
Biology open 2013 Jul 15;2(7):647-59
Biology open 2013 Jul 15;2(7):647-59
Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development.
Zarbalis K, Siegenthaler JA, Choe Y, May SR, Peterson AS, Pleasure SJ
Proceedings of the National Academy of Sciences of the United States of America 2007 Aug 28;104(35):14002-7
Proceedings of the National Academy of Sciences of the United States of America 2007 Aug 28;104(35):14002-7
Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome.
Dagenais SL, Hartsough RL, Erickson RP, Witte MH, Butler MG, Glover TW
Gene expression patterns : GEP 2004 Oct;4(6):611-9
Gene expression patterns : GEP 2004 Oct;4(6):611-9
Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.
Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF, Sarfarazi M, Burnand KG, Jeffery S, Mortimer P, Murday VA
Journal of medical genetics 2002 Jul;39(7):478-83
Journal of medical genetics 2002 Jul;39(7):478-83
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Supportive validation
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- WB
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- WB
Supportive validation
- Submitted by
- antibodies-online (provider)
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- Experimental details
- IHC
- Submitted by
- antibodies-online (provider)
- Main image
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- IHC
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- IHC