FOXP2 抗体 (C-Term)
Quick Overview for FOXP2 抗体 (C-Term) (ABIN6295056)
抗原
See all FOXP2 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 657-684, C-Term
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原理
- Rabbit Anti-FOXP2 (C-term) Antibody
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免疫原
- This FOXP2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 657-684 amino acids from the C-terminal region of human FOXP2.
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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 641-740) antibodyFOXP2 适用: 人 WB, ELISA, FACS 宿主: 小鼠 Monoclonal 2G11B8 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
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限制
- 仅限研究用
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储存条件
- 4 °C,-20 °C
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储存方法
- 2-8°C (short-term), -20°C (long-term)
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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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Target Description: FOXP2 is 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.
Gene Symbol: FOXP2
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基因ID
- 93986
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UniProt
- O15409
抗原
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