CAOPORN成人免费公开,欧美FREESEX黑人又粗又大 ,欧美狠狠入鲁的视频777色,主仆调教SM束缚绳索捆绑

掃碼關(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
真人一进一出120秒试看,两个人免费观看视频,每日更新在线观看av
Rabbit Anti-RAD50/BF594 Conjugated antibody (bs-11230R-BF594)
訂購熱線:400-901-9800
訂購郵箱:sales@www.tjshangbang.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@www.tjshangbang.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-11230R-BF594
英文名稱 Rabbit Anti-RAD50/BF594 Conjugated antibody
中文名稱 BF594標(biāo)記的DNA修復(fù)蛋白Rad50抗體
別    名 DNA repair protein RAD50; hRad50; hsRAD50; Mrell; NBSLD; Rad 50; RAD50 2; rad50; RAD50 homolog (S cerevisiae); RAD50 homolog; RAD50 PEN; RAD50_HUMAN; Rad50l; Truncated RAD50 protein.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 染色質(zhì)和核信號  表觀遺傳學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Cow, Horse, Rabbit, Sheep, )
產(chǎn)品應(yīng)用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 154kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human RAD50 (817-872aa)
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:
The protein encoded by this gene is highly similar to Saccharomyces cerevisiae Rad50, a protein involved in DNA double-strand break repair. This protein forms a complex with MRE11 and NBS1. The protein complex binds to DNA and displays numerous enzymatic activities that are required for nonhomologous joining of DNA ends. This protein, cooperating with its partners, is important for DNA double-strand break repair, cell cycle checkpoint activation, telomere maintenance, and meiotic recombination. Knockout studies of the mouse homolog suggest this gene is essential for cell growth and viability. Mutations in this gene are the cause of Nijmegen breakage syndrome-like disorder.

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. Found in a complex with TERF2. Interacts with RINT1. Interacts with BRCA1 via its N-terminal domain. Interacts with DCLRE1C/Artemis.

Subcellular Location:
Nucleus. Chromosome telomere. Localizes to discrete nuclear foci after treatment with genotoxic agents.

Tissue Specificity:
Expressed at very low level in most tissues, except in testis where it is expressed at higher level. Expressed in fibroblasts.

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

DISEASE:
Defects in RAD50 are the cause of Nijmegen breakage syndrome-like disorder (NBSLD) [MIM:613078]; also called NBS-like disorder or RAD50 deficiency. NBSLD is a disorder similar to Nijmegen breakage syndrome and characterized by chromosomal instability, radiation sensitivity, microcephaly, growth retardation, short stature and bird-like face. Immunodeficiency is absent.

Similarity:
Belongs to the SMC family. RAD50 subfamily.
Contains 1 zinc-hook domain.

Database links:

Entrez Gene: 10111 Human

Entrez Gene: 19360 Mouse

Entrez Gene: 64012 Rat

Omim: 604040 Human

SwissProt: Q92878 Human

SwissProt: P70388 Mouse

SwissProt: Q9JIL8 Rat

Unigene: 633509 Human

Unigene: 4888 Mouse

Unigene: 51136 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.www.tjshangbang.com 北京博奧森生物技術(shù)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
无码精品久久一区二区三区| 日本久久精品一区二区三区| 亚洲精华国产精华精华液网站| 国产在线观看精品一区二区三区91| 国产精品久久久久一区二区三区| 欧美人妻精品一区二区三区| 亚洲 欧美 日韩综合| 一区2区3区精品国产欧美| 乖宝真紧H嘶爽老子H| 在线伦理电影| 国产亚洲人成网站在线观看琪琪秋| 日韩不卡1卡2卡三卡免费网站2021| 国产视频一二三区| 国产精品亚洲专区无码第一页| 国产综合精品| 成人依依大香蕉| 超碰97人人做人人爱网站| 目黑めぐみ人妻中文字幕| 131美女爱做视频午夜免费| 亚洲成A人片在线观看无遮挡| 日韩一区二区三区精品| 精品日韩一区二区三区视频| 国产麻豆剧果冻传媒白晶晶| 国产精品久久国产精品99盘| 350PAO国产成视频永久免费| 无码中文精品专区一区二区| 九九国产精品无码免费视频| 国产精品美女久久久久久| 无码国产精品一区二区免费式直播 | 人妻少妇啊灬啊灬用力啊快| 国产内射爽爽大片视频社区在线| 国产毛多水多高潮高清| 中国XXXXXL免费| 亚洲精品无码午夜福利中文字幕| 欧美熟妇精品一区二区三区| JK浴室自慰到不停喷水尿失禁| 国产无遮挡又爽又刺激的视频老师| 欧美日韩国产VA另类| www.春色.com| 强行入侵高清在线观看| 国产精品美女久久久久久|