FOXL2 抗体 (C-Term) (PE)
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Quick Overview for FOXL2 抗体 (C-Term) (PE) (ABIN7991466)
抗原
See all FOXL2 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- C-Term
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原理
- Anti-FOXL2 Antibody PE Conjugated
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交叉反应 （详细）
- No cross-reactivity with other proteins.
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预测反应
- identical to the related mouse sequences.
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纯化方法
- Immunogen affinity purified.
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免疫原
- A synthetic peptide corresponding to a sequence at the C-terminus of human FOXL2, identical to the related mouse sequences.
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亚型
- IgG
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anti-Forkhead Box L2 (FOXL2) (C-Term) antibody
Verified FOXL2 适用: 人, 小鼠 WB, ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
anti-Forkhead Box L2 (FOXL2) (AA 3-29), (N-Term) antibodyFOXL2 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB22898 unconjugated
anti-Forkhead Box L2 (FOXL2) antibodyFOXL2 适用: 人 WB 宿主: 兔 Monoclonal unconjugated
anti-Forkhead Box L2 (FOXL2) (C-Term) antibodyFOXL2 适用: 人, 小鼠, 大鼠, Cow, Pig, 兔, 山羊, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box L2 (FOXL2) (N-Term) antibodyFOXL2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box L2 (FOXL2) antibodyFOXL2 适用: 小鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box L2 (FOXL2) (AA 116-216) antibodyFOXL2 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box L2 (FOXL2) antibodyFOXL2 适用: 人, 小鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box L2 (FOXL2) antibodyFOXL2 适用: 人 DB 宿主: 小鼠 Monoclonal 262C1a unconjugated
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应用备注
- Flow Cytometry, Optimal dilutions should be determined by end users.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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有效期
- 12 months
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- FOXL2 (Forkhead Box L2 (FOXL2))
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别名
- FOXL2
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背景
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Background: The forkhead transcription factor gene, FOXL2 located in blepharophimosis-ptosis-epicanthus inversus syndrome(BPES) critical region on chromosome 3q23. Consistent with an involvement in BPES, FOXL2 is selectively expressed in the mesenchyme of developing mouse eyelids and in adult ovarian follicles, in adult humans, it appears predominantly in the ovary. FOXL2 haploinsufficiency may cause BPES types I and II by the effect of a null allele and a hypomorphic allele, respectively. Furthermore, in a fraction of the BPES patients the genetic defect does not reside within the coding region of the FOXL2 gene and may be caused by a position effect. FOXL2 mutations can also cause gonadal dysgenesis or premature ovarian failure(POF) in women, as well as eyelid/forehead dysmorphology in both sexes.
Gene Full Name: forkhead box L2
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基因ID
- 668
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UniProt
- P58012
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途径
- Nuclear Hormone Receptor Binding, Positive Regulation of Endopeptidase Activity
抗原
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