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  質量反饋  人才招聘  關于我們  聯(lián)系我們
99精品国产一区二区三|丰满少妇a∨一区二区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Phospho-Mre11 (Ser676)/PE-Cy5.5 Conjugated antibody (bs-3293R-PE-Cy5.5)
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  
100ul/2980.00元
大包裝/詢價
產品編號 bs-3293R-PE-Cy5.5
英文名稱1 Rabbit Anti-Phospho-Mre11 (Ser676)/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標記的磷酸化DNA損傷關鍵蛋白Mre11抗體
別    名 Mre 11; MRE 11a; MRE 11b; MRE11 homolog 1; MRE11 meiotic recombination 11 homolog A; MRE11a; MRE11b; AT like disease; Ataxia telangiectasia disorder like; Ataxia-telangiectasia disorder-like; ATLD; DNA recombination and repair protein; Double strand break repair protein MRE11A; Double-strand break repair protein MRE11A; endo/exonuclease Mre11. HNGS1; meiotic recombination (S. cerevisiae) 11 homolog A; meiotic recombination 11 homolog A (S. cerevisiae); meiotic recombination 11 homolog A; MmMRE11A.MRE11_RAT  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
產品類型 磷酸化抗體 
研究領域 腫瘤  細胞生物  免疫學  染色質和核信號  細胞凋亡  轉錄調節(jié)因子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 80kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated Synthesised phosphopeptide derived from rat Mre11 around the phosphorylation site of Ser676
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.
產品介紹 background:
This gene encodes a nuclear protein involved in homologous recombination, telomere length maintenance, and DNA double-strand break repair. By itself, the protein has 3' to 5' exonuclease activity and endonuclease activity. The protein forms a complex with the RAD50 homolog; this complex is required for nonhomologous joining of DNA ends and possesses increased single-stranded DNA endonuclease and 3' to 5' exonuclease activities. In conjunction with a DNA ligase, this protein promotes the joining of noncomplementary ends in vitro using short homologies near the ends of the DNA fragments. This gene has a pseudogene on chromosome 3. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

Function:
Component of the MRN complex, which plays a central role in double-strand break (DSB) repair, DNA recombination, maintenance of telomere integrity and meiosis. The complex possesses single-strand endonuclease activity and double-strand-specific 3'-5' exonuclease activity, which are provided by MRE11A. RAD50 may be required to bind DNA ends and hold them in close proximity. This could facilitate searches for short or long regions of sequence homology in the recombining DNA templates, and may also stimulate the activity of DNA ligases and/or restrict the nuclease activity of MRE11A to prevent nucleolytic degradation past a given point. The complex may also be required for DNA damage signaling via activation of the ATM kinase. In telomeres the MRN complex may modulate t-loop formation

Subunit:
Component of the MRN complex composed of two heterodimers RAD50/MRE11A associated with a single NBN. Component of the BASC complex, at least composed of BRCA1, MSH2, MSH6, MLH1, ATM, BLM, RAD50, MRE11A and NBN. Interacts with DCLRE1C/Artemis and DCLRE1B/Apollo.

Subcellular Location:
Nucleus. Note=Localizes to discrete nuclear foci after treatment with genotoxic agents

Post-translational modifications:
Phosphorylated upon DNA damage, probably by ATM or ATR.

DISEASE:
Defects in MRE11A are a cause of ataxia telangiectasia-like disorder (ATLD) [MIM:604391]. ATLD is a disease with the same clinical feature than ataxia-telangiectasia but with a somewhat milder clinical course.

Similarity:
Belongs to the MRE11/RAD32 family.

Database links:

Entrez Gene: 4361 Human

Entrez Gene: 17535 Mouse

Entrez Gene: 64046 Rat

Omim: 600814 Human

SwissProt: P49959 Human

SwissProt: Q61216 Mouse

SwissProt: Q9JIM0 Rat

Unigene: 192649 Human

Unigene: 149071 Mouse

Unigene: 209040 Rat



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

    在細胞中,有多種蛋白參與DNA損傷應答,DNA損傷是可引起癌變的細胞變化,這些蛋白在細胞發(fā)生損傷后會啟動細胞修復過程,幫助受損的細胞恢復正常。
    正常情況下,細胞會經歷生長、分化和自然死亡的歷程。當細胞受到損傷時,如;輻射損傷或是毒物刺激,一種多蛋白復合物參與的步驟將被啟動,進行細胞修復工作并激活其他的生物過程。在這過程中,存在一種MRN復合物,由Mre11,Rad50和NBS1蛋白組成,MRN探測DNA損傷(DNA雙鏈是否斷裂)的情況。復合物在探測到DNA損傷信號后將把這個信息傳遞給一種酶,ATM(ataxia-telangiectasia mutated)檢測激酶(checkpoint kinase)。ATM激酶能對DNA雙鏈斷裂產生應答反應,它具有降低細胞增殖的能力,給細胞修復騰出時間。因此ATM一旦發(fā)生變異,功能失效可能導致免疫缺陷甚至是癌變。
    研究者認為,Mre11不僅是DNA損傷的感受器,更是修復DNA的啟動因子,還能修飾受損的DNA分子。
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
欧美大片一区二区三区| 欧美精品A∨在线观看| 蜜桃成熟1997| 午夜av一区二区三区中文字幕| 色一情一乱一乱一区99AV| 国产大波爆乳在线观看| 乌克兰少妇XXXX做受野外| 正在播放4p国产4P| 亚洲AV无码专区国产不卡顿 | 黑人异族巨大巨大巨粗| 少妇伦子伦精品无码STYLES| 88国产精品欧美一区二区三区 | 欧美人体大胆瓣开下部自慰| 女同日韩精品一区二区亚洲av| 亚洲欧美1区2区3区4区| 人与禽性视频77777| 成人做爰WWW免费看视频日本| 人人妻人人爽人人澡黄色| 欧美一区二区爽大粗| 女厕厕露P撒尿八个少妇| 老师穿着旗袍肉色丝袜让我玩| 欧洲站特大码胖MM潮流女装| 三级三级久久三级久久18| 精品国产911在线观看| 久久婷婷激情五月天| 玩弄JAPAN白嫩少妇HD小说| 久久免费看美女高潮视频| 日本亚洲色大成网站WWW久久| 国产亚洲综合成年人在线| YYY6080韩国三级理论| 亚洲AV片不卡无码久久 | 国精品久久久久久久久人妻| 国产剧情AV片醉酒女邻居| 日本女同一区二区中文字幕| 2021国产精品久久| 亚洲国产精品无码久久久| aaa亚洲男人天堂一区| 国产又粗又猛又黄又爽无遮挡| 麻豆国产AV超爽剧情系列| 久久综合伊人| 日韩精品无码一区二区三区视频 |