FOXC1 抗体 (AA 101-200)
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- 抗原 See all FOXC1 抗体
- FOXC1 (Forkhead Box C1 (FOXC1))
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抗原表位
- AA 101-200
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适用
- 人, 小鼠, 大鼠, 山羊
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This FOXC1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 山羊, 人, 小鼠, 大鼠
- 预测反应
- Dog,Cow,Horse,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FOXC1/FREAC3
- 亚型
- IgG
- Top Product
- Discover our top product FOXC1 Primary Antibody
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anti-Forkhead Box C1 (FOXC1) (C-Term) antibody
Verified FOXC1 适用: 人 ELISA, IF, FACS 宿主: 山羊 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) antibodyFOXC1 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (AA 1-79) antibodyFOXC1 适用: 人 WB, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (Center) antibodyFOXC1 适用: 人, 小鼠, 大鼠, 小鸡 WB, IHC, IF, IC 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (AA 62-186) antibodyFOXC1 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) antibodyFOXC1 适用: 人, 小鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (C-Term) antibodyFOXC1 适用: 人, 小鼠, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (AA 464-553) antibodyFOXC1 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4D11 unconjugated
anti-Forkhead Box C1 (FOXC1) (AA 406-455) antibodyFOXC1 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (Internal Region) antibodyVerified FOXC1 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
ELISA 1:500-1000
FCM 1:20-100
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- FOXC1 (Forkhead Box C1 (FOXC1))
- 别名
- FREAC3 (FOXC1 产品)
- 别名
- ARA antibody, FKHL7 antibody, FREAC-3 antibody, FREAC3 antibody, IGDA antibody, IHG1 antibody, IRID1 antibody, RIEG3 antibody, FoxC1 antibody, fkhl7 antibody, freac-3 antibody, freac3 antibody, igda antibody, ihg1 antibody, irid1 antibody, rieg3 antibody, xfd-11 antibody, ara antibody, FOXC1 antibody, foxc1 antibody, Fkh1 antibody, Mf1 antibody, Mf4 antibody, ch antibody, fkh-1 antibody, frkhda antibody, CFKH-1 antibody, XFD-11 antibody, foxc1.2 antibody, id:ibd5079 antibody, forkhead box C1 antibody, forkhead box C1 S homeolog antibody, forkhead box C1 L homeolog antibody, Forkhead box protein C1 antibody, winged helix transcription factor XFD-11 antibody, forkhead box C1b antibody, FOXC1 antibody, Foxc1 antibody, foxc1.S antibody, foxc1 antibody, foxc1.L antibody, foxc1-A antibody, foxc1b antibody
- 背景
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Synonyms: ARA, FKH L7, FKHL 7, FKHL7, Forkhead Drosophila like 7, Forkhead, forkhead box C1, Forkhead box protein C1,Forkhead drosophila homolog like 7, Forkhead like 7, Forkhead related activator 3, Forkhead related protein FKHL7, Forkhead related transcription factor 3, Forkhead-related protein FKHL7, Forkhead-related transcription factor 3, FOX C1, FOXC 1, FOXC1, FOXC1_HUMAN, FREAC 3,FREAC-3, FREAC3, homolog-like 7, IGDA, IHG 1, IHG1, IRID 1, IRID1, Iridogoniodysgenesis type 1, Myeloid factor delta.
Background: Binding of FREAC-3 and FREAC-4 to their cognate sites results in bending of the DNA at an angle of 80-90 degrees.Involvement in disease, Defects in FOXC1 are the cause of Axenfeld-Rieger syndrome type 3 (RIEG3), also known as Axenfeld-Rieger syndrome (ARS) or Axenfeld syndrome or Axenfeld anomaly. It is characterized by posterior corneal embryotoxon, prominent Schwalbe line and iris adhesion to the Schwalbe line. Other features may be hypertelorism (wide spacing of the eyes), hypoplasia of the malar bones, congenital absence of some teeth and mental retardation. When associated with tooth anomalies, the disorder is known as Rieger syndrome. Glaucoma is a progressive blinding condition that occurs in approximately half of patients with Axenfeld-Rieger malformations.
- 基因ID
- 2296
- 途径
- Chromatin Binding, Glycosaminoglycan Metabolic Process
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