產(chǎn)品編號 | bs-3955R-Cy5 |
英文名稱 | Rabbit Anti-MT-ND6/Cy5 Conjugated antibody |
中文名稱 | Cy5標(biāo)記的NADH復(fù)合體6抗體 |
別 名 | Mitochondrially encoded NADH dehydrogenase 6; NADH-ubiquinone oxidoreductase chain 6; MT ND6; mtND6; NADH dehydrogenase subunit 6 (complex I); NADH dehydrogenase subunit 6; NADH ubiquinone oxidoreductase chain 6; NADH Ubiquinone Oxidoreductase subunit ND6; NADH6; ND6; NU6M_HUMAN; NU6M_HUMAN. |
規(guī)格價格 | 100ul/2980元 購買 大包裝/詢價 |
說 明 書 | 100ul |
研究領(lǐng)域 | 腫瘤 細(xì)胞生物 免疫學(xué) 神經(jīng)生物學(xué) 轉(zhuǎn)錄調(diào)節(jié)因子 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | Human, Rat, (predicted: Mouse, Dog, Cow, Horse, Sheep, ) |
產(chǎn)品應(yīng)用 | IF=1:50-200
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 19kDa |
性 狀 | Lyophilized or Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human MTND6 |
亞 型 | IgG |
純化方法 | affinity purified by Protein A |
儲 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
保存條件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
產(chǎn)品介紹 |
background: NADH Dehydrogenase subunit 6 (MTND6) is 1 of the 7 mitochondrial DNA (mtDNA) encoded subunits (MTND1, MTND2, MTND3, MTND4L, MTND4, MTND5, MTND6) included among the approximately 41 polypeptides of respiratory Complex I. Complex I accepts electrons from NADH, transfers them to ubiquinone (Coenzyme Q10), and uses the energy released to pump protons across the mitochondria inner membrane. MTND6 has been proposed to be a component of the iron-protein fragment. Function: Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone (By similarity). Subcellular Location: Mitochondrion membrane; Multi-pass membrane protein (Potential). DISEASE: Defects in MT-ND6 are a cause of Leber hereditary optic neuropathy (LHON) [MIM:535000]. LHON is a maternally inherited disease resulting in acute or subacute loss of central vision, due to optic nerve dysfunction. Cardiac conduction defects and neurological defects have also been described in some patients. LHON results from primary mitochondrial DNA mutations affecting the respiratory chain complexes. Defects in MT-ND6 are a cause of Leber hereditary optic neuropathy with dystonia (LDYT) [MIM:500001]; also called familial dystonia with visual failure and striatal lucencies. LDYT is part of a spectrum of Leber hereditary optic neuropathy. It is characterized by the association of optic atrophy and central vision loss with dystonia. Defects in MT-ND6 are a cause of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome (MELAS) [MIM:540000]. MELAS is a genetically heterogenious disorder, characterized by episodic vomiting, seizures, and recurrent cerebral insults resembling strokes and causing hemiparesis, hemianopsia, or cortical blindness. Defects in MT-ND6 are a cause of mitochondrial complex I deficiency (MT-C1D) [MIM:252010]. A disorder of the mitochondrial respiratory chain that causes a wide range of clinical manifestations from lethal neonatal disease to adult-onset neurodegenerative disorders. Phenotypes include macrocephaly with progressive leukodystrophy, non-specific encephalopathy, cardiomyopathy, myopathy, liver disease, Leigh syndrome, Leber hereditary optic neuropathy, and some forms of Parkinson disease. Similarity: Belongs to the complex I subunit 6 family. Database links: Entrez Gene: 4541 Human Omim: 516006 Human SwissProt: P03923 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 亚洲精品国产成人综合久久久久久久久 | 性感女性黄色免费观看视频破解版 | 污开车视频免费在线观看 | 影音先锋av资源网站 | 国产一级婬片A片鲁大师 | 精品秘 一区二三区免费雷安 | 鲁鲁狠狠狠7777一区二区 | 2024理论片在线看片免费 | 无码人妻一区二区三区免费京洛会 | 97国产揄拍国产精品 | 91丝袜精品久久久久久无码人妻 | 日本一级婬片A片AAA毛片价格 | 99久久久无码国产精品免费四季 | 亚洲高清免费观看 | 玩弄丰满老熟妇BBBBB | 17C嫩嫩草色视频蜜桃 | A级性感美女道一本有码在线播放 | 欧美成人免费视频网址 | 亚洲中文字幕在线观看 | 成人网站精品99xyz | 蜜臀久久99精品久久久久久白杨根 | 精选品国产自线拍 | 搡老女人老91妇女老熟女 | 国产伦精品一区二区三区免费 | 午夜成人精品一二三区 | 无码人妻丰满少妇熟妇区五十路 | 欧美黑人一级爽快片婬片高清 | 久久久91人妻无码精品蜜桃成人电影 | 女人被狂躁C到高潮视频 | 手机无码视频一区二区三区 | 一级婬片120分钟试看好 | 人人做人人添A片久久精品 亚洲无码中文字幕在线观看 | 久久精品在线视频网站在线视频 | 黄片在线免费观看高清 | 黑人午夜性猛交久久久 | 快日啊爽快视频交换草穴刺激欧美激情 | 中文字幕一区二区三区四区 | 哈尔滨熟女白浆91九色 | AV一区二区三区四区 | 国产护士囗交吞精视频 |