Forkhead Box C1 抗体
(Forkhead Box C1 (FOXC1))
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. [provided by RefSeq, Jul 2008].
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58 results
FOXC1
适用: 人, 小鼠, 大鼠, 小鸡
WB, IHC, IF, IC
宿主: 兔
Polyclonal
unconjugated
FOXC1
适用: 人, 小鼠, 大鼠, 山羊
WB, ELISA, FACS, IHC (p), IF (cc), IF (p), IHC (fro)
宿主: 兔
Polyclonal
unconjugated
1 image
FOXC1
适用: 人, 小鼠, 大鼠
WB, ELISA, IHC, IF
宿主: 兔
Polyclonal
unconjugated
1 image
FOXC1
适用: 人, 小鼠, 大鼠, 小鸡
WB, IHC, IF, ICC, IHC (p)
宿主: 兔
Polyclonal
unconjugated
Latest Publications for our Forkhead Box C1 抗体
: "FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost." in: Investigative ophthalmology & visual science, Vol. 59, Issue 6, pp. 2548-2554, (2019) (PubMed).: "Role of FOXC1 in regulating APSCs self-renewal via STI-1/PrPC signaling." in: Theranostics, Vol. 9, Issue 22, pp. 6443-6465, (2019) (PubMed).
: "Targeting EZH2 reactivates a breast cancer subtype-specific anti-metastatic transcriptional program." in: Nature communications, Vol. 9, Issue 1, pp. 2547, (2018) (PubMed).
: "Foxc1 and Foxc2 deletion causes abnormal lymphangiogenesis and correlates with ERK hyperactivation." in: The Journal of clinical investigation, Vol. 126, Issue 7, pp. 2437-51, (2017) (PubMed).
: "Yap and Taz play a crucial role in neural crest-derived craniofacial development." in: Development (Cambridge, England), Vol. 143, Issue 3, pp. 504-15, (2016) (PubMed).
: "A mouse model of aniridia reveals the in vivo downstream targets of Pax6 driving iris and ciliary body development in the eye." in: Biochimica et biophysica acta, Vol. 1863, Issue 1, pp. 60-67, (2016) (PubMed).
: "FOXA1 deletion in luminal epithelium causes prostatic hyperplasia and alteration of differentiated phenotype." in: Laboratory investigation; a journal of technical methods and pathology, Vol. 94, Issue 7, pp. 726-39, (2014) (PubMed).
: "Dysfunction of the stress-responsive FOXC1 transcription factor contributes to the earlier-onset glaucoma observed in Axenfeld-Rieger syndrome patients." in: Cell death & disease, Vol. 5, pp. e1069, (2014) (PubMed).
: "Foxc1 is required by pericytes during fetal brain angiogenesis." in: Biology open, Vol. 2, Issue 7, pp. 647-59, (2013) (PubMed).
: "FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A." in: Human molecular genetics, Vol. 17, Issue 4, pp. 490-505, (2008) (PubMed).
Aliases for Forkhead Box C1 抗体
forkhead box C1 (FOXC1) 抗体forkhead box C1 (Foxc1) 抗体
forkhead box C1 S homeolog (foxc1.S) 抗体
forkhead box C1 (foxc1) 抗体
forkhead box C1 L homeolog (foxc1.L) 抗体
Forkhead box protein C1 (foxc1) 抗体
winged helix transcription factor XFD-11 (foxc1-A) 抗体
forkhead box C1b (foxc1b) 抗体
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xfd-11 抗体
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