Human NADH-ubiquinone oxidoreductase chain 6(MT-ND6) ELISA kit

Human NADH-ubiquinone oxidoreductase chain 6(MT-ND6) ELISA kit

產品詳情

引用文獻

產品評價

靶點詳情

產品詳情

引用文獻

產品評價

相關產品

靶點詳情

Most popular with customers

產品中心

信號通路

技術信息

聯系信息

文獻引用 (5) 說明書下載

中文名稱：

人NADH-泛醌氧化還原酶鏈6(MT-ND6)酶聯免疫試劑盒
貨號：

CSB-EL015082HU
規格：

96T/48T
價格：

￥3600/￥2500
其他：

CUSABIO Wins 2024 Bioz Rapid Star? Award in the ELISA category

產品詳情
產品評價
引用文獻
相關產品
靶點詳情

產品描述：

人NADH-泛醌氧化還原酶鏈6(MT-ND6)酶聯免疫試劑盒（CSB-EL015082HU）為雙抗夾心法ELISA試劑盒，定量檢測血清、血漿、組織勻漿、細胞裂解物樣本中的MT-ND6含量。MT-ND6是一個靶點。它在細胞呼吸鏈中有著重要地位，與氧化磷酸化過程相關。相關研究機制主要聚焦于其在能量代謝中的功能、基因突變對細胞生理功能的影響，以及與神經退行性疾病等病癥的潛在關聯，為疾病治療提供新方向。試劑盒檢測范圍為23.44 pg/mL-1500 pg/mL，適用于基礎科研中對線粒體功能的機制研究，例如探究疾病模型中線粒體能量代謝變化、評估基因編輯或藥物干預對MT-ND6表達的影響，也可用于篩選調節線粒體呼吸鏈活性的化合物。其廣泛的樣本兼容性支持跨類型實驗設計，為細胞生物學、病理生理學及代謝相關研究提供可靠工具。本品僅用于科研，不用于臨床診斷，產品具體參數及操作步驟詳見產品說明書。
別名：

MT-ND6 ELISA Kit; MTND6 ELISA Kit; NADH6 ELISA Kit; ND6 ELISA Kit; NADH-ubiquinone oxidoreductase chain 6 ELISA Kit; EC 7.1.1.2 ELISA Kit; NADH dehydrogenase subunit 6 ELISA Kit
縮寫：

MT-ND6
Uniprot No.：

P03923
種屬：

Homo sapiens (Human)
樣本類型：

serum, plasma, tissue homogenates, cell lysates
檢測范圍：

23.44 pg/mL-1500 pg/mL
靈敏度：

5.86 pg/mL
反應時間：

1-5h
樣本體積：

50-100ul
檢測波長：

450 nm
研究領域：

Signal Transduction
測定原理：

quantitative
測定方法：

Sandwich

精密度：

線性度：

To assess the linearity of the assay, samples were spiked with high concentrations of Human MT-ND6 in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.
	Sample	Serum(n=4)
1:1	Average %	92
	Range %	84-98
1:2	Average %	86
	Range %	80-92
1:4	Average %	94
	Range %	85-98
1:8	Average %	102
	Range %	98-106

回收率：

The recovery of Human MT-ND6 spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section.

Sample Type	Average % Recovery	Range
Serum (n=5)	94	88-98
EDTA plasma (n=4)	89	83-95

標準曲線：

These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.

pg/ml	OD1	OD2	Average	Corrected
1500	2.763	2.867	2.815	2.716
750	2.426	2.321	2.374	2.275
375	1.675	1.772	1.724	1.625
187.5	1.045	1.115	1.080	0.981
93.75	0.527	0.534	0.531	0.432
46.88	0.274	0.277	0.276	0.177
23.44	0.188	0.178	0.183	0.084
0	0.098	0.099	0.099

數據處理：

ELISA操作視頻及標曲繪制軟件下載
貨期：

3-5 working days

Circulating mtNFPs Are Associated with ARDS after CPB and Regulate Endothelial Barrier through FPR2 P Lu, X Li, J Wang, X Li, Z Shen, Y Qi,American Journal of Respiratory Cell and Molecular Biology,2024
Abnormal levels of mitochondrial Ca2+ channel proteins in plasma neuron‐derived extracellular vesicles of early schizophrenia EJ Goetzl,FASEB journal,2023
Measles seroprevalence among Dutch travelling families L Doornekamp,Travel Medicine and Infectious Disease,2021
Abnormal levels of mitochondrial proteins in plasma neuronal extracellular vesicles in major depressive disorder EJ Goetzl,Molecular psychiatry,2021
Decreased mitochondrial electron transport proteins and increased complement mediators in plasma neural-derived exosomes of early psychosis EJ Goetzl,translational psychiatry,2020

功能：

Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which catalyzes electron transfer from NADH through the respiratory chain, using ubiquinone as an electron acceptor. Essential for the catalytic activity and assembly of complex I.
基因功能參考文獻：
1. Study identify a significant down-expression of MT-ND6 in men with Klinefelter syndrome. PMID: 29333085
2. The molecular diagnostics by the whole exome sequencing showed a novel de novo (c.1374-2A>C) mutation in the KRT10 gene responsible for the development of IWC (KRT10 defect was confirmed by immunofluorescent study). Concurrently, the m.14484T>C mutation in mitochondrial MTND6 gene (characteristic for Leber's hereditary optic neuropathy or LHON) was detected in patient, his mother and brother PMID: 28944608
3. This review focuses on the role of mitochondrial genes in causing LHON and therapeutics available for treating the disease. A systematic search has been adopted in various databases using the keywords "LHON," "mitochondria," "ND1," "ND4," "ND6," and "therapy" and the following review on mitochondrial genetics PMID: 29133631
4. Liver MT-ND6 transcriptional activity and protein expression were decreased in nonalcoholic steatohepatitis, suggesting that the expression of this mitochondrial gene may play an important role in the disease progression. PMID: 22879518
5. This study shows that m.14484T>C arose independently in a different mtDNA haplogroup and ethnic background in India, which may influence the clinical expression of the disease. PMID: 23674761
6. These data suggested that the ND6 T14502C variant may modulate the phenotypic manifestation of the G11778A mutation in these Chinese pedigrees. PMID: 20691156
7. the G14459A mutation is a candidate mutation for maternally inherited dystonia PMID: 20052369
8. novel mitochondrial DNA nucleotide transversion, C14482A (M64I) was found to cause Leber's hereditary optic neuropathy with visual recovery PMID: 12112086
9. mitochondrial ND6 may have a role in Leber's hereditary optic neuropathy PMID: 15922297
10. Free radicals-mediated damage was studied in transmitochondrial cells harboring T14487C mutation in the ND6 gene of mtDNA. PMID: 16337195
11. Therefore, the coexistence of the A1555G mutation and T14484C mutations in this Chinese family indicate that the A1555G mutation may play a synergistic role in the phenotypic manifestation of LHON associated ND6 T14484C mutation. PMID: 17452034
12. T14484C and T14502C in ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family. PMID: 18440284
13. Molecular analysis has led to identification of the known T14502C mutation in ND6 gene in Chinese families with Leber's hereditary optic neuropathy. PMID: 19732751
14. missense mutation 14487T>C resulted in severe encephalopathies ranging from infantile Leigh syndrome to adult-onset progressive myoclonic epilepsy with dystonia in a five-generation family PMID: 20019223
顯示更多

收起更多
相關疾病：

Leber hereditary optic neuropathy (LHON); Leber hereditary optic neuropathy with dystonia (LDYT); Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome (MELAS); Mitochondrial complex I deficiency (MT-C1D)
亞細胞定位：

Mitochondrion inner membrane; Multi-pass membrane protein.
蛋白家族：

Complex I subunit 6 family
數據庫鏈接：

HGNC: 7462

OMIM: 252010

KEGG: hsa:4541

STRING: 9606.ENSP00000354665

Intra-assay Precision (Precision within an assay): CV%<8%

Three samples of known concentration were tested twenty times on one plate to assess.

Inter-assay Precision (Precision between assays): CV%<10%

Three samples of known concentration were tested in twenty assays to assess.