Analytical Data
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基因名
SLC25A4
- Application
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别名
ADP.ATP carrier protein 1;ADP.ATP carrier protein. heart/skeletal muscle isoform T1;Adenine nucleotide translocator 1;Solute carrier family 25 member 4
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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
P12235
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表达区间
2-298 aa
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氨基酸序列
GDHAWSFLKDFLAGGVAVSKTAVAPIERVKLLLQVQHASKQISAEKQYKGIIDCVVRIPKEQGFLSFWRGNLANVIRYFPTQALNFAFKDKYKQLFLGGVDRHKQFWRYFAGNLASGGGATSLCFVYPLDFARTRLDVGKGQREFHGLGDCIIKIFKSDGLRGLYQGFNVSVQGIIIYRYFGVYDTAKGMLPDPKNVHIFVSWMIAQSVTAVAGLVSYPFDTVRRRMMMQSGRKGADIMYTGTVDCWRKIAKDEGAKAFFKGAWSNVLRGMGGAFVLVLYDEIKKYV
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分子量
34.4 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
SLC25A4, also known as the adenine nucleotide translocator 1 (ANT1), is a crucial protein encoded by the SLC25A4 gene, responsible for the transport of adenine nucleotides across the mitochondrial inner membrane. This protein plays a vital role in cellular energy metabolism by facilitating the exchange of ATP and ADP between the mitochondria and the cytosol, thus influencing ATP production and mitochondrial function. The importance of SLC25A4 is underscored by its involvement in various metabolic disorders and diseases, including myopathies and mitochondrial diseases. Investigating the recombinant protein of SLC25A4 can provide insights into its structural and functional properties, aiding in the understanding of its role in cellular metabolism and potential therapeutic targets. Recent studies have focused on the characterization of SLC25A4 through recombinant expression systems, allowing researchers to analyze its transport mechanisms, interaction with other mitochondrial proteins, and impact on energy homeostasis. Furthermore, understanding the mutations and variations in the SLC25A4 gene may contribute to the development of gene therapy strategies for related mitochondrial dysfunctions. As mitochondrial dysfunction is linked to numerous diseases, including neurodegenerative disorders and cancer, the study of SLC25A4 presents significant implications for advancing therapeutic approaches and enhancing our understanding of mitochondrial biology.












