Analytical Data
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基因名
SMAD4
- Application
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别名
DPC4; JIP; MADH4; Deletion target in pancreatic carcinoma 4
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种属
Mouse
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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
P97471
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表达区间
Thr9~Ser231
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蛋白长度
Partial
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分子量
28kDa
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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
SMAD4 is a pivotal protein in the transforming growth factor-beta (TGF-β) signaling pathway, playing a crucial role in mediating cellular responses to TGF-β and related cytokines. It acts as a common mediator for signals that regulate key biological processes, including cell growth, differentiation, and apoptosis. Dysregulation of SMAD4 has been implicated in various human diseases, particularly in cancers such as pancreatic and colorectal tumors, where mutations or deletions of the SMAD4 gene are common. Research into SMAD4 recombinant proteins has gained attention as it allows for the exploration of its structural and functional properties, providing insights into the molecular mechanisms underlying TGF-β signaling. These studies enhance our understanding of cancer biology and could lead to the development of novel therapeutic strategies targeting SMAD4 and its signaling pathways. Moreover, the availability of recombinant SMAD4 proteins facilitates the study of protein interactions, post-translational modifications, and the identification of potential small molecules that can modulate its activity, promising avenues for therapeutic intervention in SMAD4-related malignancies. As the need for targeted cancer therapies intensifies, ongoing research into the characterization and functional analysis of SMAD4 recombinant proteins is vital for uncovering its potential as a biomarker and therapeutic target in clinical oncology.












