ARG64086

anti-FOXP2 antibody

anti-FOXP2 antibody for IHC-Formalin-fixed paraffin-embedded sections and Human

Gene Regulation antibody

概述

产品描述 Goat Polyclonal antibody recognizes FOXP2
反应物种 Hu
预测物种 Ms, Rat, Cat, Cow, Dog, Pig, Zfsh
应用 IHC-P
特异性 This antibody is expected to recognize isoform I (NP_055306.1), isoform II (NP_683696.2), isoform IV (NP_683698.2) and isoform V (NP_001166237.1).
宿主 Goat
克隆 Polyclonal
同位型 IgG
靶点名称 FOXP2
抗原物种 Human
抗原 C-DEVEYQKRRSQKIT
偶联标记 Un-conjugated
別名 CAG repeat protein 44; TNRC10; CAGH44; SPCH1; Forkhead box protein P2; Trinucleotide repeat-containing gene 10 protein

应用说明

应用建议
应用 推荐稀释比
IHC-P2.5 µg/ml
应用说明 IHC-P: Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0).
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

属性

形式 Liquid
纯化 Purified from goat serum by antigen affinity chromatography.
缓冲液 Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA.
抗菌剂 0.02% Sodium azide
稳定剂 0.5% BSA
浓度 0.5 mg/ml
存放说明 For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项 For laboratory research only, not for drug, diagnostic or other use.

生物信息

数据库连接

GeneID: 93986 Human FOXP2

Swiss-port # O15409 Human Forkhead box protein P2

背景介绍 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.[provided by RefSeq, Feb 2010]
研究领域 Gene Regulation antibody
预测分子量 80 kDa

检测图片 (2) Click the Picture to Zoom In

  • ARG64086 anti-FOXP2 antibody IHC-P image

    Immunohistochemistry: Paraffin-embedded Human placenta tissue. Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0). The tissue section was stained with ARG64086 anti-FOXP2 antibody at 2.5 µg/ml dilution followed by AP-staining.

  • ARG64086 anti-FOXP2 antibody IHC-P image

    Immunohistochemistry: paraffin embedded Human Prostate. (Steamed antigen retrieval with citrate buffer pH 6) stained with ARG64086 anti-FOXP2 antibody at 2.5 µg/ml dilution followed by AP-staining.