Analytical Data
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基因名
spoT
- Application
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别名
spoT；Thyroid hormone-inducible hepatic Protein
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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
P0AG24
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表达区间
1-702aa
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氨基酸序列
MYLFESLNQLIQTYLPEDQIKRLRQAYLVARDAHEGQTRSSGEPYITHPVAVACILAEMKLDYETLMAALLHDVIEDTPATYQDMEQLFGKSVAELVEGVSKLDKLKFRDKKEAQAENFRKMIMAMVQDIRVILIKLADRTHNMRTLGSLRPDKRRRIARETLEIYSPLAHRLGIHHIKTELEELGFEALYPNRYRVIKEVVKAARGNRKEMIQKILSEIEGRLQEAGIPCRVSGREKHLYSIYCKMVLKEQRFHSIMDIYAFRVIVNDSDTCYRVLGQMHSLYKPRPGRVKDYIAIPKANGYQSLHTSMIGPHGVPVEVQIRTEDMDQMAEMGVAAHWAYKEHGETSTTAQIRAQRWMQSLLELQQSAGSSFEFIESVKSDLFPDEIYVFTPEGRIVELPAGATPVDFAYAVHTDIGHACVGARVDRQPYPLSQPLTSGQTVEIITAPGARPNAAWLNFVVSSKARAKIRQLLKNLKRDDSVSLGRRLLNHALGGSRKLNEIPQENIQRELDRMKLATLDDLLAEIGLGNAMSVVVAKNLQHGDASIPPATQSHGHLPIKGADGVLITFAKCCRPIPGDPIIAHVSPGKGLVIHHESCRNIRGYQKEPEKFMAVEWDKETAQEFITEIKVEMFNHQGALANLTAAINTTTSNIQSLNTEEKDGRVYSAFIRLTARDRVHLANIMRKIRVMPDVIKVTRNRN
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分子量
86.8 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
The study of spoT recombinant proteins has gained significant attention in the field of bacterial physiology and cellular signaling. SpoT is an essential enzyme in bacteria that plays a crucial role in the synthesis and degradation of the second messenger molecule, guanosine 5'-diphosphate 3'-diphosphate (ppGpp), which is a key regulator of the stringent response—a cellular adaptation process that enables bacteria to survive nutrient starvation and other stress conditions. Understanding the functional mechanisms of SpoT and its role in ppGpp metabolism is critical, as it affects various bacterial processes including biofilm formation, virulence, and antibiotic resistance. Researchers have focused on characterizing the structure and activity of SpoT through recombinant protein techniques to elucidate its enzymatic pathways and regulatory roles. By producing spoT proteins in heterologous systems, scientists can investigate how mutations or modifications in the SpoT enzyme influence bacterial behavior and adaptiveness. Furthermore, insights gained from spoT studies hold potential implications for developing new antimicrobial strategies, as targeting this regulatory pathway could help in combating bacterial infections and resistance mechanisms. As such, the functional analysis of spoT recombinant proteins not only deepens our understanding of bacterial physiology but also offers avenues for innovative therapeutic interventions.
