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
亚洲精品无码永久在线观看,国产v片成人影院在线观看,亚洲人成网网址在线看
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-KMT1D/APC Conjugated antibody (bs-16789R-APC)
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-APC
英文名稱1 Rabbit Anti-KMT1D/APC Conjugated antibody
中文名稱 APC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: 亚洲日韩欧美不卡在线观看| 亚洲精品国产综合久久一线锤子| 波多野结衣中文在线播放99| 中国美女一级看片40分钟视频| 亚洲午夜精品久久久久久武腾凌香无码视频| 亚洲白虎一区二区白虎一线天| 久久婷婷成人综合色给合| 国产99视频精品免视看67| 亚洲黄色在线观看网站h| 久久精品国内一区二区三区_成人免费无 | 亚洲AV秘?无码一区二神宫寺| 久久久久亚洲AV成人网人人小说 | 在线观看自拍少妇精品| 人妻少妇中文字幕乱码七| mm131亚洲精品美女自拍| 无码不卡在线视频无毒| 东北老妇露脸BBBBBBBXXXXXXXHD| 亚洲国产天堂久久综合网站_中文 亚洲国产婷婷综合在线精品_亚洲国产综合精品 | 中文字幕无码少妇日日骚| 嫩草影院无码导航| 3Dh亚洲精品一区二区 | 中文字幕视频导航日韩欧美| 男人猛进猛出免费视频观看| 97精品人人妻人人玩人人做| 日韩无免费密码视频16| 91午夜精品亚洲一区二区三区密桃| 日本伊人精品一区二区三区观看方式| 高清三级视频在线播放免费| 天天爽夜夜爽夜夜爽精品视频| 苍老师高潮国产免费| 里番ACG里番本子全彩软件测评无毒不卡 | 东方美女大战黑人mp4| 色樱桃视频看看| 伊人伊成久久人综合网996,亚洲狼人| 久久精品国产96精品亚洲怡红| 国产一区二区精品久久岳,精品精品国产自在 | 亚洲一区二区三区久久久久久国产99 | av中文字幕有码资源站| 乱亲女H秽乱长久久久嫂子全文| 中文字幕一区二区三区红楼| 国产最新进精品视频1区2区3区 |