关键信息
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基因名
SLC25A37
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简介
The SLC25A37 protein is a mitochondrial iron transporter that specifically promotes iron uptake by developing erythrocytes, which is critical for heme biosynthesis. By mediating iron transport into red blood cell mitochondria, SLC25A37 supports heme synthesis, which is critical for various biological processes including hemoglobin formation. SLC25A37 Protein, Human (sf9, His, MBP, FLAG) is the recombinant human-derived SLC25A37 protein, expressed by sf9 insect cells , with N-MBP, C-Flag, N-8*His labeled tag.
- 应用
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别名
SLC25A37; Mitoferrin-1; Mitochondrial iron transporter 1; Mitochondrial solute carrier protein; Solute carrier family 25 member 37
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种属
Human
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表达系统
Baculovirus
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标签
N-MBP;C-Flag;N-8*His
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
Q9NYZ2
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表达区间
E2-Y338
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蛋白长度
Partial
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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.
质检流程
相关产品
背景信息
SLC25A37, also known as mitochondrial iron transporter 1 (MIT1), plays a critical role in maintaining mitochondrial iron homeostasis and cellular iron metabolism. Dysregulation of iron transport within mitochondria can lead to various pathophysiological conditions, including neurodegeneration, anemia, and mitochondrial diseases. The study of SLC25A37 is essential for understanding the mechanisms underlying these disorders and for developing potential therapeutic strategies. Recent research has focused on the characterization of SLC25A37 through recombinant protein expression, which allows for the investigation of its functional properties, interaction with iron, and transport mechanisms. Recombinant SLC25A37 proteins, produced in suitable expression systems, enable detailed biochemical assays, structural analyses, and functional studies, revealing insights into how this transporter operates at a molecular level. The elucidation of these mechanisms is vital, as it could pave the way for novel interventions targeting mitochondrial iron dysregulation. Current studies emphasize the importance of SLC25A37 in iron metabolism and its potential impact on various diseases, highlighting the need for continued research in this area to uncover the therapeutic potential of targeting SLC25A37 pathways.
