亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  人才招聘  關于我們  聯系我們
久久精品国产精品亚洲精品,免费无码成人av在线播放不卡,尤物在线观看精品国产福利片
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-NDUFV1/Gold Conjugated antibody (bs-3959R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產品編號 bs-3959R-Gold
英文名稱1 Rabbit Anti-NDUFV1/Gold Conjugated antibody
中文名稱 膠體金標記的NADH脫氫酶黃素蛋白1抗體
別    名 CI 51kD; Complex I 51kD; NADH dehydrogenase (ubiquinone) flavoprotein 1; NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial; NADH dehydrogenase flavoprotein 1; NADH ubiquinone oxidoreductase 51 kDa subunit; NADH ubiquinone oxidoreductase; NDUFV 1; UQOR1; NDUV1_HUMAN.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 腫瘤  細胞生物  免疫學  線粒體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, Mouse, Rat,  (predicted: Dog, Pig, Cow, Horse, )
產品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 49kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human NDUFV1
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產品介紹 background:
The mitochondrial respiratory chain provides energy to cells via oxidative phosphorylation and consists of four membrane-bound electron-transporting protein complexes (I-IV) and an ATP synthase (complex V). This gene encodes a 51 kDa subunit of the NADH:ubiquinone oxidoreductase complex I; a large complex with at least 45 nuclear and mitochondrial encoded subunits that liberates electrons from NADH and channels them to ubiquinone. This subunit carries the NADH-binding site as well as flavin mononucleotide (FMN)- and Fe-S-biding sites. Defects in complex I are a common cause of mitochondrial dysfunction; a syndrome that occurs in approximately 1 in 10,000 live births. Mitochondrial complex I deficiency is linked to myopathies, encephalomyopathies, and neurodegenerative disorders such as Parkinson's disease and Leigh syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009]

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).

Subunit:
Complex I is composed of 45 different subunits. This is a component of the flavoprotein-sulfur (FP) fragment of the enzyme.

Subcellular Location:
Mitochondrion inner membrane; Peripheral membrane protein; Matrix side.

DISEASE:
Defects in NDUFV1 are a cause of Leigh syndrome (LS) [MIM:256000]. LS is a severe neurological disorder characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions.

Similarity:
Belongs to the complex I 51 kDa subunit family.

Database links:

Entrez Gene: 287014 Cow

Entrez Gene: 4723 Human

Entrez Gene: 17995 Mouse

Entrez Gene: 293655 Rat

Omim: 161015 Human

SwissProt: P25708 Cow

SwissProt: P49821 Human

SwissProt: Q91YT0 Mouse

SwissProt: Q5XIH3 Rat

Unigene: 7744 Human

Unigene: 29842 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.www.chomd.com.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 一区二区三区视频观看传媒| 无码精品前田一区二区久久久久 | 色 五月 亚洲 综合 婷婷| 男女午夜24式免费视频网站| 国产精品久久久综合尿奴| 中日韩美中文字幕一卡二区| 四虎影视在线视频大全免费观看HD在线观看| 久久综合婷婷国产二区高清 | 暴力入室性强迫free| 亚洲经典在线中文字幕视频| 乱人伦人妻中文字幕在线,亚洲性色精品一区二区在线 | 四虎影视最新地址大全0| 精品无码国产自产拍在涩| 中文字幕无码综合插插| 女人下边被添全过视频软件国产| 国产在线观看7738区| 亚洲欧美日韩中文字幕视频屏幕 | 日韩超碰人人爽人人做人人添_| 国产一级做a爰片在线看免费,国产一区二 | 精品国产日韩热久久简单Av | 亚洲精品国产自在久久出水,精品一区二区三区四区 | 97视频热人人精品免费,银杏| 无码国产伦一区二区三区视频al换脸| 精品国产人成亚洲区-人人爽人人澡| 制服丝袜在线亚洲导航| 久久99精品久久久久久水蜜桃久 | 亚洲精品熟女国产张津瑜| 韩国专线一区二三区电影| 亚洲人成无码网站在线观看 两个奶头高潮| 人人妻人人澡人人爽人人精品97_亚洲一 | 亚洲精品久久无码老熟妇 | 国产亚洲一区二区三区在线播放香蕉视频| 一区二区9999999久| 国语自产精品视频在线看 抢先版图片| 一区二区三区视频在线播放| 国产最爽的乱婬视频国语对白| 亚洲国产熟女精品网站| 插曲在线观看免费观看高清| 免费一级无遮挡成人视频网站| 樱桃成人亚洲mv网站| 国产女人aaa级久久久级|久久精品人妻无码一区二区三区 |