FOXP2 antibody [GT12812]-单抗-深圳欣博盛生物科技有限公司

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FOXP2 antibody [GT12812]

品牌：GeneTex

官网链接

说明书

折扣/货期

货号：GTX635965	规格：100μl	目录价：￥4000
货号：GTX635965-S	规格：25μl	目录价：￥1700

产品详情

* 以下信息仅供参考，详情请以原厂网站为准

产品名称:

FOXP2 antibody [GT12812]

别名:

forkhead box P2 , CAGH44 , SPCH1 , TNRC10

反应种属:

Human, Mouse

宿主来源:

Mouse

实验应用:

IHC-P, WB

同种型:

IgG1

免疫原:

Recombinant protein encompassing a sequence within the N-terminus region of human FOXP2. The exact sequence is proprietary.

克隆性:

Monoclonal

克隆号:

GT12812

纯化方式:

Affinity purified by Protein G.

偶联:

Unconjugated

产品浓度:

1 mg/ml (Please refer to the vial label for the specific concentration.)

保存温度:

Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.

运输温度:

4°C

预期分子量:

产品形式:

Liquid

存储溶液:

PBS, 20% Glycerol, no preservatives.

生产商:

GeneTex

功能与背景:

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]

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