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
天天躁夜夜躁狠狠躁2021,特级毛片www俄罗斯免,亚洲av无码无在线观看红杏
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-KMT1D/Cy3 Conjugated antibody (bs-16789R-Cy3)
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  
100ul/2980.00元
大包裝/詢價
產品編號 bs-16789R-Cy3
英文名稱1 Rabbit Anti-KMT1D/Cy3 Conjugated antibody
中文名稱 Cy3標記的賴氨酸N甲基轉移酶1D/EHMT1抗體
別    名 bA188C12.1; DKFZp667M072; EHMT 1; EHMT1; EHMT1_HUMAN; Eu-HMTase1; Eu HMTase1; Euchromatic histone lysine N methyltransferase 1; Euchromatic histone methyltransferase 1; Euchromatic histone-lysine N-methyltransferase 1; EUHMTASE1; FLJ12879; FP13812; G9a like protein 1; G9a like protein; G9a-like protein 1; GLP 1; GLP; GLP1; H3 K9 HMTase 5; H3-K9-HMTase 5; Histone H3 K9 methyltransferase 5; Histone H3-K9 methyltransferase 5; Histone lysine N methyltransferase H3 lysine 9 specific 5; Histone-lysine N-methyltransferase EHMT1; KIAA1876; Lysine N methyltransferase 1D; Lysine N-methyltransferase 1D; RP11 188C12.1.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
產品類型 甲基化抗體 
研究領域 細胞生物  細胞周期蛋白  膠原蛋白  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Cow, Rabbit, )
產品應用 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 141kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human KMT1D
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:
The protein encoded by this gene is a histone methyltransferase that is part of the E2F6 complex, which represses transcription. The encoded protein methylates the Lys-9 position of histone H3, which tags it for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

Function:
Histone methyltransferase that specifically mono- and dimethylates 'Lys-9' of histone H3 (H3K9me1 and H3K9me2, respectively) in euchromatin. H3K9me represents a specific tag for epigenetic transcriptional repression by recruiting HP1 proteins to methylated histones. Also weakly methylates 'Lys-27' of histone H3 (H3K27me). Also required for DNA methylation, the histone methyltransferase activity is not required for DNA methylation, suggesting that these 2 activities function independently. Probably targeted to histone H3 by different DNA-binding proteins like E2F6, MGA, MAX and/or DP1. During G0 phase, it probably contributes to silencing of MYC- and E2F-responsive genes, suggesting a role in G0/G1 transition in cell cycle. In addition to the histone methyltransferase activity, also methylates non-histone proteins: mediates dimethylation of 'Lys-373' of p53/TP53.

Subcellular Location:
Nucleus. Chromosome. Associates with euchromatic regions.

Tissue Specificity:
Widely expressed.

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

DISEASE:
Defects in EHMT1 are the cause of chromosome 9q subtelomeric deletion syndrome (9q- syndrome) [MIM:610253]. Common features seen in these patients are severe mental retardation, hypotonia, brachy(micro)cephaly, epileptic seizures, flat face with hypertelorism, synophrys, anteverted nares, cupid bow or tented upper lip, everted lower lip, prognathism, macroglossia, conotruncal heart defects, and behavioral problems.

Similarity:
Belongs to the histone-lysine methyltransferase family.
Contains 8 ANK repeats.
Contains 1 pre-SET domain.
Contains 1 SET domain.

Database links:

Entrez Gene: 79813 Human

Entrez Gene: 77683 Mouse

Omim: 607001 Human

SwissProt: Q9H9B1 Human

SwissProt: Q5DW34 Mouse

Unigene: 495511 Human

Unigene: 24176 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: 精品久久久久久中文幕人妻葵司 | 亚洲国产无线乱码在线观看 | AI特级婬片内谢AAA片自拍| 91视频电影网一区| 午夜精品视频91一区二区三区| 亚洲熟妇vs亚洲熟妇AV| 欧美日韩在线无吗av免费线路一 | 久久男人av资源网站,午夜人性色| 国产成人精品午夜福麻豆报告麻豆| 樱桃视频成人AV| 久久人人爽人人爽人人AV麻 | 日韩精品无码久久一区二区三27页| 国产尤物在线观看亚洲一区二区| 国产一区二区不卡老阿姨苍井空 | 东北老妇露脸xXXXX| 亚洲AV无码专区电影在线观看,BDSM| 亚洲国产美女精品久久久久黑暗圣经 | 国产熟女口爆视屏| 亚洲字幕在线观看000| 无码人妻精品一区二区三区久久久后入第一视角 - v8 | 久久久久久国精品色费色费s| 91久久午夜无码鲁丝片久久人妻 | 优优优优优色视频| 久久9精品区-无套内射无码母子| 中文字幕不卡在线8页| 久久精品国产乱子伦多人1集| 一区二区三区视频免费观看猎奇| 精品无码av专区一区二区河山| 一级毛片一级毛片一级毛片AAAB | 丝袜亚洲AV微信| 18禁止看的免费污网站APP | 国产成人精品曰本亚洲78_第1集| 无码少妇中文字幕日韩| 成人免费久久久66 | 亚洲美女又黄又爽在线观看穿越| 激情综合婷婷丁香五月国产老妇女| 亚洲日韩精品秘?在线观看| 国产美女精品一区二区三区免费下载 | 国产亚洲人成网站在线观看l_第1集| 亚洲老熟妇伦理电影| 国产911视频精品|