Analytical Data
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基因名
ACSS3
- Application
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别名
ACSS3；Acyl-CoA synthetase short-chain family member 3. mitochondrial
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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
Q9H6R3
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表达区间
30-686aa
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氨基酸序列
AGAALRALVVPGPRGGLGGRGCRALSSGSGSEYKTHFAASVTDPERFWGKAAEQISWYKPWTKTLENKHSPSTRWFVEGMLNICYNAVDRHIENGKGDKIAIIYDSPVTNTKATFTYKEVLEQVSKLAGVLVKHGIKKGDTVVIYMPMIPQAMYTMLACARIGAIHSLIFGGFASKELSSRIDHVKPKVVVTASFGIEPGRRVEYVPLVEEALKIGQHKPDKILIYNRPNMEAVPLAPGRDLDWDEEMAKAQSHDCVPVLSEHPLYILYTSGTTGLPKGVIRPTGGYAVMLHWSMSSIYGLQPGEVWWAASDLGWVVGHSYICYGPLLHGNTTVLYEGKPVGTPDAGAYFRVLAEHGVAALFTAPTAIRAIRQQDPGAALGKQYSLTRFKTLFVAGERCDVETLEWSKNVFRVPVLDHWWQTETGSPITASCVGLGNSKTPPPGQAGKSVPGYNVMILDDNMQKLKARCLGNIVVKLPLPPGAFSGLWKNQEAFKHLYFEKFPGYYDTMDAGYMDEEGYLYVMSRVDDVINVAGHRISAGAIEESILSHGTVADCAVVGKEDPLKGHVPLALCVLRKDINATEEQVLEEIVKHVRQNIGPVAAFRNAVFVKQLPKTRSGKIPRSALSAIVNGKPYKITSTIEDPSIFGHVEEMLKQA
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分子量
77.9 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
ACSS3 (Acetyl-CoA synthetase 3) is an enzyme that plays a critical role in cellular metabolism by catalyzing the conversion of acetate into acetyl-CoA, a central metabolite involved in various biosynthetic pathways and energy production. Recent studies have highlighted the importance of ACSS3 in regulating metabolic processes, particularly in conditions such as obesity, cancer, and neurodegenerative diseases. The reprogramming of acetate metabolism has garnered significant attention, as aberrant acetyl-CoA levels can influence histone acetylation and gene expression, thereby altering cellular signaling and functionality. Research into ACSS3 has progressed in understanding its structure-function relationship, regulatory mechanisms, and potential therapeutic implications. Developing ACSS3-targeted therapies could offer novel strategies for manipulating metabolic pathways in disease contexts. Scientists are investigating the enzyme’s role in metabolic adaptation under stress and its interaction with other cellular pathways, further elucidating its significance in health and disease. This body of work aims to establish ACSS3 not only as a metabolic enzyme but also as a possible biomarker and therapeutic target for conditions characterized by metabolic dysregulation.
