吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

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
老旺的大肉蟒进进出出,天天躁日日躁狠狠躁AV中文 ,国产麻豆剧传媒精品国产AV
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-KMT1D/AP Conjugated antibody (bs-16789R-AP)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-16789R-AP
英文名稱1 Rabbit Anti-KMT1D/AP Conjugated antibody
中文名稱 堿性磷酸酶(AP)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(guī)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 WB=1:50-200 IHC-P=1:50-200 IHC-F=1:50-200 ICC=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.xucheq.com 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
日韩精品一区二区三区色欲AV| 365天今时之欲| 国产精品一区二区AV| 嗯快点别停舒服好爽受不了了 | 大又大粗又爽又黄少妇毛片| 精品国产成人亚洲午夜福利| 人妻少妇精品中文字幕av蜜桃 | 少妇人妻偷人精品一区二区| 无码a片| 天堂在\/线中文官网| 蜜臀AV在线播放| 国产AV无码专区亚洲AV毛网站| 女教师の爆乳BD在线观看| 亚洲AV无码一区二区一二区| 久久久久久久女国产乱让韩| 国产精品久久久久久久久久免费 | 白洁被高振干到九点多| 亚洲啪AV永久无码精品放毛片| 特黄三级又爽又粗又大| 日韩亚洲AV人人夜夜澡人人爽| 和尚吮她的花蒂和奶水视频 | 久久久久99精品成人片直播| 亚洲精品国产成人| 久久无码人妻精品一区二区三区| 亚洲AV无码AV制服丝袜在线| 丰满少妇大力进入AV亚洲| 无码人妻精品一区二区三区不卡 | 精品亚洲麻豆1区2区3区| WWW亚洲精品少妇裸乳一区二区| 少妇夹得好紧太爽了A片| 色视频WWW在线播放国产人成| zzijzzij亚洲日本少妇jizjiz| 看同性男AA片| 日本护士毛茸茸| 99热久久这里只精品国产WWW| 亚洲国产成人精品无码区二本| 久久丫精品国产亚洲AV| 精品久久香蕉国产线看观看亚洲 | 99精品久久99久久久久| 国产麻豆精品一区二区三区| 亚洲国产一区二区三区|