Analytical Data
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基因名
FOXP1
- Application
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别名
FOXP1；Forkhead box Protein P1
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种属
Human
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表达系统
E. coli
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标签
His tag N-Terminus
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
Q9H334-5
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表达区间
1-114aa
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氨基酸序列
MMQESGTETKSNGSAIQNGSGGSNHLLECGGLREGRSNGETPAVDIGAAD LAHAQQQQQQWHLINHQPSRSPSSWLKRLISSPWELEVLQVPLWGAVAET KMSGPVCQPNPSPF
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分子量
38 kDa
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内毒素
< 1.0 EU per μg protein as determined by the LAL method.
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性状
Freeze-dried powder
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缓冲液
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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复溶方法
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- 个性化定制
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稳定性测试
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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保存条件 & 期限
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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运输条件
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
Related Products
Protein Description
FOXP1, a member of the forkhead box family of transcription factors, plays a crucial role in various biological processes, including development, immune response, and brain function. Dysregulation of FOXP1 has been associated with several disorders, including autism spectrum disorders and intellectual disabilities, highlighting its importance in normal human development and function. The study of FOXP1 recombinant proteins aims to elucidate its structural and functional properties, as well as its interaction with other proteins and genomic elements. By producing and characterizing FOXP1 recombinant proteins, researchers can gain insights into its transcriptional regulatory mechanisms and the pathways it influences. Additionally, these studies may help identify potential therapeutic targets for diseases linked to FOXP1 mutations or dysfunctions. Given the complexity of FOXP1's role in various cell types, including lymphocytes and neurons, understanding its function at the molecular level through recombinant protein studies is essential for advancing our knowledge of its biological significance and potential implications in disease contexts.
