91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
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  關于我們  聯(lián)系我們
无码人妻丰满熟妇精品区东京直播 ,黄色视频在线观看网站
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-GLE1/PE-Cy5.5 Conjugated antibody (bs-13371R-PE-Cy5.5)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-13371R-PE-Cy5.5
英文名稱 Rabbit Anti-GLE1/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標記的核孔蛋白GLE1抗體
別    名 GLE 1; GLE1; GLE1 like protein; GLE1 like RNA export mediator; GLE1 RNA export mediator homolog; GLE1 RNA export mediator like (yeast); GLE1-like protein; GLE1_HUMAN; GLE1L; hGLE1; LCCS 1; LCCS; LCCS1; Nucleoporin GLE1.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 染色質(zhì)和核信號  信號轉導  轉運蛋白  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Rat,  (predicted: Human, Mouse, Dog, Pig, Cow, Horse, Sheep, )
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 80kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GLE1
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:
Protein transport across the nucleus is a selective, multi-step process involving several cytoplasmic factors that mediate protein passage through the nuclear pore complex (NPC). Gle1, also known as GLE1L, is a 698 amino acid protein that localizes to both the nucleus and the cytoplasm and belongs to the Gle1 family. Expressed as two alternatively spliced isoforms, Gle1 associates with the NPC and is required for the transport of poly(A)-containing mRNAs from the nucleus to the cytoplasm. Defects in the gene encoding Gle1 are the cause of lethal congenital contracture syndrome type 1 (LCCS1) and lethal arthrogryposis with anterior horn cell disease (LAAHD), the former of which is characterized by early fetal hydrops and akinesia, micrognatia, pulmonary hypoplasia, pterygia and prenatal death, while the latter is associated with respiratory failure.

Function:
Required for the export of mRNAs containing poly(A) tails from the nucleus into the cytoplasm. May be involved in the terminal step of the mRNA transport through the nuclear pore complex (NPC).

Subunit:
Associated with the NPC, it however may not be a stable component of the NPC complex since it shuttles between the nucleus and the cytoplasm. Interacts with nuclear pore complex proteins NUP155 and NUPL2. Isoform 2 does not interact with NUPL2. Able to form a heterotrimer with NUP155 and NUPL2 in vitro.

Subcellular Location:
Nucleus. Cytoplasm. Shuttles between the nucleus and the cytoplasm. Shuttling is essential for its mRNA export function and Cytoplasm. Nucleus > nuclear pore complex. Shuttles between the nucleus and the cytoplasm. In the nucleus, isoform 1 localizes to the nuclear pore complex and nuclear envelope. Shuttling is essential for its mRNA export function.

DISEASE:
Defects in GLE1 are the cause of lethal congenital contracture syndrome type 1 (LCCS1) [MIM:253310]; also known as multiple contracture syndrome type Finnish. LCCS is an autosomal recessive disorder characterized by early fetal hydrops and akinesia, micrognatia, pulmonary hypoplasia, pterygia, multiple joint contractures, specific neuropathology with degeneration of anterior horn neurons and extreme skeletal muscle atrophy. LCCS1 leads to prenatal death. Defects in GLE1 are the cause of lethal arthrogryposis with anterior horn cell disease (LAAHD) [MIM:611890]. LAAHD is characterized by fetal akinesia, arthrogryposis and motor neuron loss. LAADH fetus often survive delivery, but die early as a result of respiratory failure. Neuropathological findings resemble those of LCCS1, but are less severe.

Similarity:
Belongs to the GLE1 family.

Database links:

Entrez Gene: 2733 Human

Entrez Gene: 74412 Mouse

Entrez Gene: 362098 Rat

GenBank: BC030012 Human

Omim: 603371 Human

SwissProt: Q53GS7 Human

SwissProt: Q8R322 Mouse

SwissProt: Q4KLN4 Rat

Unigene: 522418 Human

Unigene: 275121 Mouse

Unigene: 162648 Rat



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 rvdoil.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
这里只有精品视频 | 黃色一级A一片人与 | 97人妻人人做人碰人人添图片 | 久久午夜精品人妻一区二区三区 | 爆 喷水 捆绑在线观看 | 欧美成人精品在线观看 | 午夜福利视频一区二区 | 欧美国产日韩一区二区 | 久久视频在线观看欧美性爱 | Porn成熟HD国产 | 国产又大又粗又猛视频 | 国产乱XXⅩXX国语对白 | 国产激情久久久久久一级A片老师 | 四房色播五月天激情电影 | 久久夜色精品国产欧美乱极品 | 女人腿张开让男人桶爽肌肌 | 人人妻人人澡人人精品 | www久久久久久久久久 | 欧美性爱XXXX黑人XYX性爽 | 成人电影在线观看网址 | 国产AⅤ无码一区二区 | 国产黃色A片三級熟女 | 少妇与大狼拘作爱视频 | 国产福利姬喷白浆流水小说 | 黄色视频免费的网站 | 国产对白粗大硬爽视频 | www.99re| 久久久久99精品成人网站3d | 91丰满熟女嗷嗷叫抽搐 | 国产做受6高潮A片91 | 波多野结衣AV无码流出 | 污网站高清无码在线观看 | 亚洲成人精品久久久 | 免费一级无码婬片A片APP直播 | 久久精品人妻一区二区蜜桃 | 一级婬片A片AAAA毛片A级 | 91人妻人人操人人爽 | 国产精品成人无码a 无码 | 成人做爰黄A片免费 | 四虎成人免费视频在线观看 | 国产成人综合日韩精品无码香 |