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  關于我們  聯系我們
熟妇人妻不卡中文字幕,欧美变态另类刺激,亚洲av午夜成人片精品网站
首頁 > 產品中心 > 一抗 > 產品信息
phospho-NBN (Ser343) Rabbit pAb (bs-6125R)  
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
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價

產品編號 bs-6125R
英文名稱 phospho-NBN (Ser343) Rabbit pAb
中文名稱 磷酸化DNA修復蛋白NBS1抗體
別    名 p95 NBS1(phospho S343); p95 NBS1(phospho Ser343); p-p95 NBS1(phospho S343); p95 NBS1; Nijmegen breakage syndrome 1; Nijmegen breakage syndrome 1(nibrin); AT V1; AT V2; AT-V1; AT-V2; ATV; Cell cycle regulatory protein p95; NBS 1; NBS; NBS1; Nibrin; Nijmege  
產品類型 磷酸化抗體 
研究領域 腫瘤  細胞生物  染色質和核信號  細胞周期蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human (predicted: Rat,Rabbit)
產品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 85 kDa
檢測分子量
細胞定位 細胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthesised phosphopeptide derived from human NBS1 around the phosphorylation site of Ser343: SL(p-S)QG 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 Component of the MRE11/RAD50/NBN (MRN complex) which plays a critical role in the cellular response to DNA damage and the maintenance of chromosome integrity. The complex is involved in double-strand break (DSB) repair, DNA recombination, maintenance of telomere integrity, cell cycle checkpoint control 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. NBN modulate the DNA damage signal sensing by recruiting PI3/PI4-kinase family members ATM, ATR, and probably DNA-PKcs to the DNA damage sites and activating their functions. It can also recruit MRE11 and RAD50 to the proximity of DSBs by an interaction with the histone H2AX. NBN also functions in telomere length maintenance by generating the 3' overhang which serves as a primer for telomerase dependent telomere elongation. NBN is a major player in the control of intra-S-phase checkpoint and there is some evidence that NBN is involved in G1 and G2 checkpoints. The roles of NBS1/MRN encompass DNA damage sensor, signal transducer, and effector, which enable cells to maintain DNA integrity and genomic stability.

Function:
Component of the MRE11-RAD50-NBN (MRN complex) which plays a critical role in the cellular response to DNA damage and the maintenance of chromosome integrity. The complex is involved in double-strand break (DSB) repair, DNA recombination, maintenance of telomere integrity, cell cycle checkpoint control 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. NBN modulate the DNA damage signal sensing by recruiting PI3/PI4-kinase family members ATM, ATR, and probably DNA-PKcs to the DNA damage sites and activating their functions. It can also recruit MRE11 and RAD50 to the proximity of DSBs by an interaction with the histone H2AX. NBN also functions in telomere length maintenance by generating the 3' overhang which serves as a primer for telomerase dependent telomere elongation. NBN is a major player in the control of intra-S-phase checkpoint and there is some evidence that NBN is involved in G1 and G2 checkpoints. The roles of NBS1/MRN encompass DNA damage sensor, signal transducer, and effector, which enable cells to maintain DNA integrity and genomic stability. Forms a complex with RBBP8 to link DNA double-strand break sensing to resection.

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 and MRE11A (By similarity). Interacts with histone H2AFX this requires phosphorylation of H2AFX on 'Ser-139'. Interacts with HJURP, INTS3, KPNA2 and TERF2. Interacts with RBBP8; the interaction links the role of the MRN complex in DNA double-strand break sensing to resection. Interacts with SP100; recruits NBN to PML bodies.

Subcellular Location:
Nucleus. Nucleus, PML body. Chromosome, telomere. Note=Localizes to discrete nuclear foci after treatment with genotoxic agents.

Tissue Specificity:
Ubiquitous. Expressed at high levels in testis.

Post-translational modifications:
Phosphorylated by ATM in response of ionizing radiation, and such phosphorylation is responsible intra-S phase checkpoint control and telomere maintenance.

DISEASE:
Nijmegen breakage syndrome (NBS) [MIM:251260]: A disorder characterized by chromosomal instability, radiation sensitivity, microcephaly, growth retardation, immunodeficiency and predisposition to cancer, particularly to lymphoid malignancies. Note=The disease is caused by mutations affecting the gene represented in this entry.
Breast cancer (BC) [MIM:114480]: A common malignancy originating from breast epithelial tissue. Breast neoplasms can be distinguished by their histologic pattern. Invasive ductal carcinoma is by far the most common type. Breast cancer is etiologically and genetically heterogeneous. Important genetic factors have been indicated by familial occurrence and bilateral involvement. Mutations at more than one locus can be involved in different families or even in the same case. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.
Aplastic anemia (AA) [MIM:609135]: A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. It is characterized by peripheral pancytopenia and marrow hypoplasia. Note=Disease susceptibility may be associated with variations affecting the gene represented in this entry.
Note=Defects in NBN might play a role in the pathogenesis of childhood acute lymphoblastic leukemia (ALL).

Similarity:
Contains 1 BRCT domain.
Contains 1 FHA domain.

SWISS:
O60934

Gene ID:
4683

Database links:

Entrez Gene: 4683 Human

Entrez Gene: 27354 Mouse

Entrez Gene: 85482 Rat

Omim: 602667 Human

SwissProt: O60934 Human

SwissProt: Q9R207 Mouse

SwissProt: Q9JIL9 Rat

Unigene: 492208 Human

Unigene: 20866 Mouse

Unigene: 25214 Rat



產品圖片
Sample: Lane 1: Human K562 cell lysates Lane 2: Human HepG2 cell lysates Lane 3: Human 293T cell lysates Lane 4: Human A549 cell lysates Primary: Anti-phospho-NBN (Ser343) (bs-6125R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 85 kDa Observed band size: 100 kDa
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: 日韩人妻无码一区二区三区99久久视频| 人妻尝试又大又粗久久精品| 国产免费久久精品99久久,亚洲中文久久久久 | 中文字幕亚洲专区日韩专区一区二区三区| 色婷婷狠狠五月综合舔| 久久久无码少妇超碰| YJLZZJLZZ亚洲乱码熟妇| 亚洲精品自在在线观看 绿帽 | 国产成人精品视频2024| 亚洲一区二区三区在线观看网站视频 | 一色屋精品视频在线观看17c视频在线观看| 亚洲乱码少妇99P-=三四区| 久久久久久久综合狠狠综合 香蕉| 国产成人久久久精品二区三区AV| 亚洲熟妇Hp视频| 精品国产77777在线观看| 亚洲中文字幕无码久久2048| 久久久久久久久久福利潮喷 | 懂色av蜜臀av粉嫩av分享吧a17| 亚洲区小说区图片区政府| 国精品无码一区二区三区在线,在线...| 69久久夜色精品国产69乱现在观看 | 竹菊精品久久久久久久yy| 人妻无码中文字幕按摩番号| 波多野42部无码喷潮在线田舍| 无码人妻AV免费一区二区三区_久久先| 国产亚洲精品资源在线在线播放| 亚洲日本一本道久久| 国产亚洲精品久久777777黑寡妇| 亚洲国产人久久综合区蜜| 国产色情综合五月丁香的特点| 亚州熟妇AV专区| ass亚洲熟妇毛茸茸|iOcs| 另类TS人妖一区二区三区| 伊人蕉久影院212| 国产日本Av电影合集| 日韩一二三毛片红挑| 在线播放无码高潮的视频| 精品国产一区二区三区久久久狼无限看亮点 | 亚洲精品秘?一区二区三区福利 | 一本一道久久a久久精品逆3p |