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琥珀酸脫氫酶復(fù)合體A亞基(SDHA)活性蛋白

Active Succinate Dehydrogenase Complex Subunit A (SDHA)

SDH2; SDHF; FP; Flavoprotein; Flavoprotein subunit of complex II; Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial

  • 琥珀酸脫氫酶復(fù)合體A亞基(SDHA)活性蛋白產(chǎn)品包裝(模擬)
  • 琥珀酸脫氫酶復(fù)合體A亞基(SDHA)活性蛋白產(chǎn)品包裝(模擬)
  • APJ784Mu01.jpgFigure. SDS-PAGE
  • Certificate通過(guò)ISO 9001、ISO 13485質(zhì)量體系認(rèn)證

活性實(shí)驗(yàn)

Succinate Dehydrogenase Complex Subunit A (SDHA) is an integral protein of the succinate dehydrogenase complex, also known as Complex II in the mitochondrial respiratory chain. It has the active site with flavin adenine dinucleotide (FAD) that catalyzes the oxidation of succinate to fumarate, playing a key role in the tricarboxylic acid (TCA) cycle and electron transport, which contributes to ATP production for cellular energy needs.SDHA binds to Succinate Dehydrogenase Complex Subunit B (SDHB) to form a stable structure, ensuring the proper assembly and function of Complex II for efficient electron transfer and metabolic reactions.Thus a functional ELISA assay was conducted to detect the interaction of recombinant mouse SDHA and recombinant mouse SDHB.
Briefly, SDHA was diluted serially in PBS with 0.01% BSA (pH 7.4). Duplicate samples of 100 μl were then transferred to SDHB-coated microtiter wells and incubated for 1h at 37℃. Wells were washed with PBST and incubated for 1h with anti-SDHA pAb, then aspirated and washed 3 times. After incubation with HRP labelled secondary antibody for 1h at 37℃, wells were aspirated and washed 5 times. With the addition of substrate solution, wells were incubated 15-25 minutes at 37℃. Finally, add 50 μL stop solution to the wells and read at 450/630nm immediately. The binding activity of recombinant mouse SDHA and recombinant mouse SDHB was shown in Figure 1, and this effect was in a dose dependent manner.

用法

Reconstitute in 10mM PBS (pH7.4) to a concentration of 0.1-1.0 mg/mL. Do not vortex.

儲(chǔ)存

避免反復(fù)凍融。2-8°C不超過(guò)一個(gè)月,-80°C不超過(guò)12個(gè)月。

穩(wěn)定性

熱穩(wěn)定性以損失率顯示。損失率是由加速降解試驗(yàn)決定,具體方法如下:在37°C孵育48小時(shí),沒(méi)有顯著的降解或者沉淀產(chǎn)生。保質(zhì)期內(nèi),在適當(dāng)?shù)臈l件下存儲(chǔ),損失率低于5%。

相關(guān)產(chǎn)品

編號(hào)適用物種:Mus musculus (Mouse,小鼠)應(yīng)用(僅供研究使用,不用于臨床診斷!)
RPJ784Mu01琥珀酸脫氫酶復(fù)合體A亞基(SDHA)重組蛋白Positive Control; Immunogen; SDS-PAGE; WB.
RPJ784Mu02琥珀酸脫氫酶復(fù)合體A亞基(SDHA)重組蛋白Positive Control; Immunogen; SDS-PAGE; WB.
APJ784Mu01琥珀酸脫氫酶復(fù)合體A亞基(SDHA)活性蛋白Cell?culture;?Activity?Assays.
PAJ784Mu01琥珀酸脫氫酶復(fù)合體A亞基(SDHA)多克隆抗體WB; IHC; ICC/IF
PAJ784Mu02琥珀酸脫氫酶復(fù)合體A亞基(SDHA)多克隆抗體WB; IHC; ICC; IP.
MAJ784Mu21琥珀酸脫氫酶復(fù)合體A亞基(SDHA)單克隆抗體WB; ICC/IF
MAJ784Mu22琥珀酸脫氫酶復(fù)合體A亞基(SDHA)單克隆抗體WB; ICC/IF
MAJ784Mu23琥珀酸脫氫酶復(fù)合體A亞基(SDHA)單克隆抗體WB; ICC/IF
MAJ784Mu24琥珀酸脫氫酶復(fù)合體A亞基(SDHA)單克隆抗體ICC/IF
SEJ784Mu琥珀酸脫氫酶復(fù)合體A亞基(SDHA)檢測(cè)試劑盒(酶聯(lián)免疫吸附試驗(yàn)法)Enzyme-linked immunosorbent assay for Antigen Detection.
LMJ784Mu琥珀酸脫氫酶復(fù)合體A亞基(SDHA)等多因子檢測(cè)試劑盒(流式熒光發(fā)光法)FLIA Kit for Antigen Detection.

參考文獻(xiàn)

雜志參考文獻(xiàn)
Cell Stem CellMacrophage-derived extracellular succinate licenses neural stem cells to suppress chronic neuroinflammation[Pubmed:29478844]