Analytical Data
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基因名
AAV2gp07
- Application
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别名
AAV2gp07；
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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
A0A513ZUU9
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表达区间
1-533aa
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氨基酸序列
MATGSGAPMADNNEGADGVGNSSGNWHCDSTWMGDRVITTSTRTWALPTYNNHLYKQISSQSGASNDNHYFGYSTPWGYFDFNRFHCHFSPRDWQRLINNNWGFRPKRLSFKLFNIQVKEVTQNDGTTTIANNLTSTVQVFTDSEYQLPYVLGSAHQGCLPPFPADVFMVPQYGYLTLNNGSQAVGRSSFYCLEYFPSQMLRTGNNFTFSYTFEDVPFHSSYAHSQSLDRLMNPLIDQYLYYLSRTNTPSGTTTMSRLQFSQAGASDIRDQSRNWLPGPCYRQQRVSKTAADNNNSDYSWTGATKYHLNGRDSLVNPGPAMASHKDDEEKYFPQSGVLIFGKQDSGKTNVDIEKVMITDEEEIRTTNPVATEQYGSVSTNLQSGNTQAATSDVNTQGVLPGMVWQDRDVYLQGPIWAKIPHTDGHFHPSPLMGGFGLKHPPPQILIKNTPVPANPSTTFSAAKFASFITQYSTGQVSVEIEWELQKENSKRWNPEIQYTSNYNKSVNVDFTVDTNGVYSEPRPIGTRYLTRNL
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分子量
64.0 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
AAV2gp07 is a recombinant protein derived from the adeno-associated virus (AAV), specifically tailored for gene therapy applications. AAVs are widely studied due to their safety profile and ability to deliver genetic material to a variety of cell types without causing pathogenic effects. The AAV2 serotype is particularly notable for its transduction efficiency in human cells. The gp07 variant incorporates specific modifications to enhance the viral capsid properties, improving its ability to bind to target cells and facilitate gene delivery. Research into AAV2gp07 focuses on its potential for therapeutic interventions in genetic disorders, where precise gene replacement or correction is critical. Studies have demonstrated its capability to overcome limitations associated with natural AAV vectors, such as immune recognition and tissue tropism. By employing advanced techniques like directed evolution and rational design, scientists aim to optimize AAV2gp07 for enhanced targeting, lower immunogenicity, and improved therapeutic outcomes. This progress is pivotal as it could lead to better treatment options for conditions such as inherited retinal diseases, muscular dystrophies, and other genetic disorders, thereby paving the way for the future of precision medicine and gene therapy.
