来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

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(zhì)量反饋  人才招聘  關于我們  聯(lián)系我們
美女脱了内裤张开腿让男人桶网站|天天狠天天透天干天天怕∴|国产CHINESE男男GAY片
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-SDHC/Gold Conjugated antibody (bs-8530R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術支持:techsupport@73327.net
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-8530R-Gold
英文名稱1 Rabbit Anti-SDHC/Gold Conjugated antibody
中文名稱 膠體金標記的琥珀酸細胞色素亞基B560抗體
別    名 mitochondrial; QPs1; C560_HUMAN; CYBL; Integral membrane protein CII-3; QPs-1; sdhC; Succinate dehydrogenase complex subunit C; Succinate dehydrogenase cytochrome b560 subunit; Succinate dehydrogenase cytochrome b560 subunit, mitochondrial precursor; Succinate-ubiquinone oxidoreductase cytochrome B large subunit.  
規(guī)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  發(fā)育生物學  神經(jīng)生物學  信號轉導  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, )
產(chǎn)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 15kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Succinate dehydrogenase complex subunit C/SDHC
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(chǎn)品介紹 background:
Membrane-anchoring subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone.

Function:
Membrane-anchoring subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q).

Subunit:
Component of complex II composed of four subunits: the flavoprotein (FP) SDHA, iron-sulfur protein (IP) SDHB, and a cytochrome b560 composed of SDHC and SDHD.

Subcellular Location:
Mitochondrion inner membrane.

DISEASE:
Defects in SDHC are the cause of paragangliomas type 3 (PGL3) [MIM:605373]. A neural crest tumor usually derived from the chromoreceptor tissue of a paraganglion. Paragangliomas are most commonly located in the head and neck region, specifically at the carotid bifurcation, the jugular foramen, the vagal nerve, and in the middle ear.
Defects in SDHC are a cause of paraganglioma and gastric stromal sarcoma (PGGSS) [MIM:606864]; also known as Carney-Stratakis syndrome. Gastrointestinal stromal tumors may be sporadic or inherited in an autosomal dominant manner, alone or as a component of a syndrome associated with other tumors, such as in the context of neurofibromatosis type 1 (NF1). Patients have both gastrointestinal stromal tumors and paragangliomas. Susceptibility to the tumors was inherited in an apparently autosomal dominant manner, with incomplete penetrance.

Similarity:
Belongs to the cytochrome b560 family.

Database links:

Entrez Gene: 327696 Cow

Entrez Gene: 6391 Human

Entrez Gene: 66052 Mouse

Entrez Gene: 100524676 Pig

Entrez Gene: 289217 Rat

Omim: 602413 Human

SwissProt: P35720 Cow

SwissProt: Q99643 Human

SwissProt: Q9CZB0 Mouse

SwissProt: D0VWV4 Pig

Unigene: 444472 Human

Unigene: 198138 Mouse

Unigene: 1698 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

Involvement in disease:Defects in SDHC are the cause of hereditary paragangliomas type 3 (PGL3) [MIM:605373]; also known as autosomal dominant non-chromaffin paragangliomas type 3. Non-chromaffin paragangliomas are usually benign, neural crest derived tumors of parasympathetic ganglia.
Defects in SDHC are a cause of paraganglioma and gastric stromal sarcoma (PGGSS) ; also known as Carney-Stratakis syndrome. Gastrointestinal stromal tumors may be sporadic or inherited in an autosomal dominant manner, alone or as a component of a syndrome associated with other tumors, such as in the context of neurofibromatosis type 1 (NF1). Patients have both gastrointestinal stromal tumors and paragangliomas. Susceptibility to the tumors was inherited in an apparently autosomal dominant manner, with incomplete penetrance.
版權所有 2004-2026 www.73327.net 北京博奧森生物技術有限公司
通過國際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫(yī)療器械-質(zhì)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(wǎng)安備110107000727號
又白又嫩毛又多15P| 免费的视频APP网站| 女人与公拘交酡全过程| 亚洲午夜福利国产精品| 黑人巨茎和中国美女视频| 熟妇人妻AV无码一区二区三区| 国产国语老龄妇女a片| 香肠派对比赛服| 91蜜臀综合99国产区| 67194熟妇在线观看线路1| AAAAA级少妇高潮大片免费看| 久久久久久精品国产欧美乱妇高清| 年轻18GAY白嫩青少年| 超碰人人澡人摸人人添| 亚洲日本在线观看午夜视频| 女人高潮真实叫床声MP3| 2018高清日本一道国产-在| CHINESE性内射高清国产| 性色AV蜜臀AV色欲AV| 欧美一区二区三区在线不卡| 亚洲学生妹嫩嫩12p| 丁香色欲久久久久久综合网| 欧美日本一品道一区二区三区| 热RE99久久精品国产99热 | 亚洲人妻精品一区二区三区| 亚洲欧美日韩综合精品久久| 国产亚洲精品合集久久久久| 欧美大片一区二区三区| 欧美日韩国产一二三四区永久在线| 亚洲色婷婷五月色晴天图片| 久久久久久夜夜夜猛噜噜| 欧美激情一区二区三区国产| WWW国产精品内射老熟女| 无码粉嫩虎白一线天在线观看| 高清VPSWINDOWS另类乱| 国产精品久久久久久22岁| 成人免费777777被爆出| GOGOGO日本免费观看视频| 精产国品一二三产区区别在线观看 | 中国丰满人妻VIDEOSHD| 日本一区二区不卡在线国产|