FOXP2 抗体 (AA 637-715)
Quick Overview for FOXP2 抗体 (AA 637-715) (ABIN5518915)
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 637-715
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原理
- Anti-FOXP2 Antibody Picoband®
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交叉反应 （详细）
- No cross-reactivity with other proteins.
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产品特性
- Anti-FOXP2 Antibody Picoband® (ABIN5518915). Tested in WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E. coli-derived human FOXP2 recombinant protein (Position: L637-E715). Human FOXP2 shares 100% amino acid (aa) sequence identity with both mouse and rat FOXP2.
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亚型
- IgG
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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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应用备注
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Western blot, 0.1-0.5 μg/mL, Human, Mouse, Rat
1. Bruce, H. A., Margolis, R. L. FOXP2: novel exons, splice variants, and CAG repeat length stability. Hum. Genet. 111: 136-144, 2002. 2. Enard, W., Przeworski, M., Fisher, S. E., Lai, C. S. L., Wiebe, V., Kitano, T., Monaco, A. P., Paabo, S. Molecular evolution of FOXP2, a gene involved in speech and language. Nature 418: 869-872, 2002. 3. Haesler, S., Wada, K., Nshdejan, A., Morrisey, E. E., Lints, T., Jarvis, E. D., Scharff, C. FoxP2expression in avian vocal learners and non-learners. J. Neurosci. 24: 3164-3175, 2004. -
说明
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We recommend Enhanced Chemiluminescent Kit with anti-Rabbit IgG (ABIN921124) for Western blot.
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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浓度
- 500 μg/mL
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缓冲液
- Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg 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
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Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated 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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Synonyms: Forkhead box protein P2,CAG repeat protein 44,Trinucleotide repeat-containing gene 10 protein,FOXP2,CAGH44, TNRC10,
Tissue Specificity: Isoform 1 and isoform 6 are expressed in adult and fetal brain, caudate nucleus and lung. .
Background: Forkhead box protein P2 (FOXP2) is a protein that, in humans, is encoded by the FOXP2 gene. 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 ly 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.
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分子量
- 90 kDa
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基因ID
- 93986
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UniProt
- O15409
抗原
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