FOXP2 抗体 (AA 657-684)
(2 references)-
- 抗原 See all FOXP2 抗体
- FOXP2 (Forkhead Box P2 (FOXP2))
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抗原表位
- AA 657-684
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适用
- 人, 小鼠
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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 FOXP2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (IF)
- 预测反应
- Rat
- 纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- 免疫原
- This FOXP2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 657-684 amino acids of human FOXP2.
- 克隆位点
- RB21207
- 亚型
- IgG
- Top Product
- Discover our top product FOXP2 Primary Antibody
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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, Pig, 犬, 兔, 马, 斑马鱼, 山羊 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) (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) (Internal Region) antibodyVerified FOXP2 适用: 人 ELISA, IHC 宿主: 山羊 Polyclonal 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
- IF: 1:10~50. WB: 1:1000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: 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
- Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
- 有效期
- 6 months
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: "Spatial rearrangement of Purkinje cell subsets forms the transverse and longitudinal compartmentalization in the mouse embryonic cerebellum." in: The Journal of comparative neurology, Vol. 525, Issue 14, pp. 2971-2990, (2018) (PubMed).
: "Clustered fine compartmentalization of the mouse embryonic cerebellar cortex and its rearrangement into the postnatal striped configuration." in: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 32, Issue 45, pp. 15688-703, (2012) (PubMed).
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: "Spatial rearrangement of Purkinje cell subsets forms the transverse and longitudinal compartmentalization in the mouse embryonic cerebellum." in: The Journal of comparative neurology, Vol. 525, Issue 14, pp. 2971-2990, (2018) (PubMed).
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- 抗原
- FOXP2 (Forkhead Box P2 (FOXP2))
- 别名
- FOXP2 (FOXP2 产品)
- 别名
- CAGH44 antibody, SPCH1 antibody, TNRC10 antibody, 2810043D05Rik antibody, AI449000 antibody, CAG-16 antibody, D0Kist7 antibody, RGD1559697 antibody, FOXP2 antibody, spch1 antibody, cagh44 antibody, tnrc10 antibody, xlFoxP2 antibody, foxP2 antibody, foxP antibody, Foxp2 antibody, foxP2b antibody, foxp2a antibody, forkhead box P2 antibody, lmw-gs antibody, forkhead box transcription factor antibody, forkhead box P2 L homeolog antibody, FOXP2 antibody, Foxp2 antibody, foxp2 antibody, foxP2 antibody, foxp1c antibody, foxp2.L antibody
- 背景
- 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.
- 分子量
- 79919
- 基因ID
- 93986
- NCBI登录号
- NP_001166237, NP_001166238, NP_055306, NP_683696, NP_683697, NP_683698
- UniProt
- O15409
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