Analytical Data
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基因名
C3orf22
- Application
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别名
C3orf22; CC022_HUMAN; Chromosome 3 open reading frame 22; Uncharacterized Protein C3orf22
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种属
Human
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表达系统
E. coli
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标签
GST-tag at N-terminal
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
Q8N5N4
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表达区间
1-141aa
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氨基酸序列
MDSSACKKSH QSKKWRIQAQ ENFAKKFPYR LSWLTEPDPE PLQPWEVTND SNTVQLPLQK RLVPTRSIPV RGLGAPDFTS PSGSCPAPLP APSPPPLCNL WELKLLSRRF PRQLAFLLST RHTEAACPQT SKAAGLSRGL S
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分子量
42.1 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
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Protein Description
C3orf22, also known as Chromosome 3 Open Reading Frame 22, has garnered attention in the field of molecular biology and genetics due to its potential role in various physiological and pathological processes. Located on chromosome 3, this gene encodes a protein that is believed to be involved in cell signaling, membrane dynamics, and possibly immune responses. Initial studies suggest that the C3orf22 protein may interact with other cellular proteins, influencing processes such as cell proliferation and differentiation. Moreover, emerging evidence indicates that variants or aberrations in the C3orf22 gene could be associated with certain diseases, including neurodegenerative disorders and cancers, thereby underscoring its importance in human health. Research involving C3orf22 has utilized advanced techniques such as CRISPR-Cas9 gene editing, RNA sequencing, and proteomics to elucidate its function and significance. Understanding the biological role of C3orf22 and its potential dysregulation in disease states may provide valuable insights into new therapeutic targets and strategies. As studies continue to unfold, the investigation into the C3orf22 protein offers promising avenues for further exploration in the realms of genetics, cellular biology, and medical research.
