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(zhì)量反饋  人才招聘  關于我們  聯(lián)系我們
国产成人午夜高潮毛片,妻子4免费完整版中文版
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-DENND4A/PE-Cy5.5 Conjugated antibody (bs-14272R-PE-Cy5.5)
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(chǎn)品編號 bs-14272R-PE-Cy5.5
英文名稱1 Rabbit Anti-DENND4A/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標記的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.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  轉(zhuǎn)運蛋白  結合蛋白  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Cow, Horse, )
產(chǎn)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 209kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human DENND4A
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:
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.

Database links:

Entrez Gene: 10260 Human

Omim: 600382 Human

SwissProt: Q7Z401 Human

Unigene: 654567 Human



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(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
国产精品无码电影在线观看 | 国产99久久久国产精品免费看| 国产成人一区二区三区影| B站禁止转播404入口| 国产激情无码一区二区三区| 国自产拍偷拍精品啪啪模特| 亚洲精品无码久久久久| 国产精品久久久久一区二区三区共| 99久久久无码国产AAA精品| 一本一道人人妻人人妻αV| 女人扒开屁股桶爽30分钟| 邻居少妇张开双腿让我爽一夜 | 国产欧美日韩精品丝袜高跟鞋| 日韩精品一区二区亚洲AV| 亚洲人成人无码网WWW国产| 国产一区二区精品久久岳| 天天躁人人躁人人躁狂躁| 国产看黄网站又黄又爽又色| 激情欧美日韩一区二区| 亚洲AV无码国产综合专区 | 午夜不卡AV免费| 孕妇滴着奶水做着爱A| 欧美 丝袜 自拍 制服 另类| 熟女肥臀白浆大屁股一区二区| 国产一区二区三区成人欧美日韩在线观看| 中文无码人妻有码人妻中文字幕| 国产精久久一区二区三区| 晚上看B站直播APP| 免费视频网站| 亚洲精华国产精华精华液网站| 亚洲AV无码专区在线播放中文| 亚洲精品无码MV在线观看| 97亚洲狠狠色综合久久久久| 午夜精品久久久久久毛片| 久久精品国产精品国产精品污| 欧美性色黄大片A级毛片视频| 国产精品宅男擼66M3U8| 精品香蕉一区二区三区| 日本无遮挡边做边爱边摸| 日韩三级| 小浪货腿张开水好多呀H|