FOXP2 抗体 (AA 641-740)
Quick Overview for FOXP2 抗体 (AA 641-740) (ABIN5542318)
抗原
See all FOXP2 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 641-740
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原理
- FOXP2 Antibody
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纯化方法
- Purified antibody
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免疫原
- Purified recombinant fragment of human FOXP2 (AA: 641-740) expressed in E. Coli.
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亚型
- IgG1
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anti-Forkhead Box P2 (FOXP2) (C-Term) antibody
Verified FOXP2 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Forkhead Box P2 (FOXP2) (AA 616-715) antibodyFOXP2 适用: 人 WB, ELISA, IF 宿主: 小鼠 Monoclonal 1F8 unconjugated
anti-Forkhead Box P2 (FOXP2) antibodyFOXP2 适用: 人 ELISA 宿主: 小鼠 Monoclonal 5C11A8 unconjugated
anti-Forkhead Box P2 (FOXP2) (N-Term) antibodyFOXP2 适用: 人, 小鼠, 大鼠, 犬, Pig, 兔, 马, 山羊, 斑马鱼 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box P2 (FOXP2) (AA 416-715) antibodyFOXP2 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box P2 (FOXP2) (Internal Region) antibodyVerified FOXP2 适用: 人 ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
anti-Forkhead Box P2 (FOXP2) (AA 71-120) antibodyFOXP2 适用: 人, 大鼠, Pig, 兔, Bat, 猴 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box P2 (FOXP2) (AA 657-684) antibodyFOXP2 适用: 人, 小鼠 WB, IF 宿主: 兔 Polyclonal RB21207 unconjugated
anti-Forkhead Box P2 (FOXP2) (AA 657-684) antibodyFOXP2 适用: 人, 小鼠 WB, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box P2 (FOXP2) antibodyFOXP2 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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应用备注
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ELISA: 1/10000
FCM: 1/200 - 1/400
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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
- Purified antibody in PBS with 0.05 % 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
- 4 °C,-20 °C
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储存方法
- Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
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- FOXP2 (Forkhead Box P2 (FOXP2))
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别名
- FOXP2
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背景
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This gene encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Multiple alternative transcripts encoding different isoforms have been identified in this gene.
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分子量
- 80 kDa
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基因ID
- 93986
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UniProt
- O15409
抗原
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