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(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  人才招聘  關(guān)于我們  聯(lián)系我們
又硬又粗进去爽A片免费,欧美精品视频
首頁 > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
Rabbit Anti-DENND4A  antibody (bs-14272R)  
~~~促銷代碼KT202411~~~
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說明書: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價(jià)
產(chǎn)品編號 bs-14272R
英文名稱 Rabbit Anti-DENND4A  antibody
中文名稱 DENND4A蛋白抗體
別    名 C-myc promoter-binding protein; DENN domain-containing protein 4A; DENN/MADD domain containing 4A; DENND4A; FLJ33949; IRLB; KIAA0476; MYCPBP; MYCPP_HUMAN.  
研究領(lǐng)域 細(xì)胞生物  轉(zhuǎn)運(yùn)蛋白  結(jié)合蛋白  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,Dog,Horse)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 209kDa
細(xì)胞定位 細(xì)胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human DENND4A: 1751-1863/1863 
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(xiàng) This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.

Function:
Binds to ISRE-like element (interferon-stimulated response element) of MYC P2 promoter.

Subcellular Location:
Nucleus.

Tissue Specificity:
Expressed ubiquitously. Highest expression in bone marrow, medium in peripheral blood lymphocytes and lowest in spleen. In brain, breast, and prostate, higher expression was seen in normal cells than in tumor cells. Expression is regulated in a growth- and cell cycle-dependent manner.

Similarity:
Contains 1 dDENN domain.
Contains 1 DENN domain.
Contains 1 MABP domain.
Contains 2 PPR (pentatricopeptide) repeats. Contains 1 uDENN domain.

SWISS:
Q7Z401

Gene ID:
10260

Database links:

Entrez Gene: 10260 Human

Omim: 600382 Human

SwissProt: Q7Z401 Human

Unigene: 654567 Human



版權(quán)所有 2004-2026 www.xucheq.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
亚洲精品乱码久久久久蜜桃| 欧美性狂猛XXXXXBBBBB| 隔着内裤揉搓她的花蒂H漫画 | 色欲狠狠躁天天躁无码中文字幕| 老熟女草BX×| 一区二区三区中文字幕| 暴虐SM灌浣肠调教A片男男| 亚洲国产成人精品女人久久久| 午夜精品久久久久久久| 亚洲精品无码久久毛片 | 偷窥美女洗澡一区二区三区| 色偷偷人人澡人人爽人人模| 久久精品| 甜蜜惩罚我是看守专用宠物| 国产真人无遮挡作爱免费视频| 日本乱妇乱熟乱妇乱色A片| 国产免费观看久久黄AV片| 好大好硬好深好爽想要 叫床| 国自产拍偷拍精品啪啪| 中文精品无码中文字幕无码专区| 亚洲国产精品无码久久| 亚洲精品一区三区三区在线观看 | 国产婷婷色一区二区三区| 女人张开腿让男人桶爽| 香蕉久久一区二区不卡无毒影院| 国产乡下妇女做爰| 精产国品一二三产区| 久久亚洲AV午夜福利精品一区| 后入内射国产一区二区| 久久精品国产亚洲7777| 人妻少妇被猛烈进入中文字幕| 国产乱人伦偷精品视频免下载| 久久精品一区二区三区中文字幕| 少妇一夜三次一区二区| 用舌头去添高潮无码视频| 亚洲欧美精品午睡沙发| 国产69精品久久久久| 中文字幕亚洲一区二区VA在线| 风韵多水的老熟妇| 人妻丰满精品一区二区A片| 日韩人妻精品一区二区三区视频 |