Analytical Data
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基因名
CC2D1A
- Application
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别名
FREUD-1; MRT3; AKI1; Mental Retardation,Nonsyndromic,Autosomal Recessive 3; Five prime repressor element under dual repression-binding 1; Akt kinase-interacting protein 1
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种属
Human
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表达系统
E. coli
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标签
N-His
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
Q6P1N0
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表达区间
Pro675~Ser944
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分子量
34kDa
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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
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Protein Description
CC2D1A (CC2 domain-containing protein 1A) is a recently identified protein that plays a crucial role in various cellular processes, including endocytosis, signal transduction, and neuronal function. Research into CC2D1A has gained attention due to its implication in several neurological disorders, particularly its association with intellectual disability and developmental delays. Studies suggest that CC2D1A is involved in the regulation of synaptic function and integrity, highlighting its potential importance in neurodevelopmental pathways. The protein features multiple functional domains, including coiled-coil and CC2 domains, which support its interaction with other proteins and cellular components. Understanding the structure and function of CC2D1A through recombinant protein studies could provide insights into its molecular mechanisms and biological roles. Additionally, exploring the effects of CC2D1A mutations can enhance our comprehension of the genetic basis of related conditions. Overall, the investigation of CC2D1A, particularly through recombinant protein expression and characterization, holds promise for unveiling fundamental aspects of neuronal biology and developing targeted therapeutic strategies for associated disorders.
