强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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  關(guān)于我們  聯(lián)系我們
www.91av,鲁大师影院中文字幕,蜜桃91精品秘 入口
首頁 > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
GLE1 Rabbit pAb (bs-13371R)  
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價(jià)

產(chǎn)品編號 bs-13371R
英文名稱 GLE1 Rabbit pAb
中文名稱 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.  
研究領(lǐng)域 染色質(zhì)和核信號  信號轉(zhuǎn)導(dǎo)  轉(zhuǎn)運(yùn)蛋白  表觀遺傳學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Rat (predicted: Human,Mouse,Pig,Sheep,Cow,Dog,Horse)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 80 kDa
檢測分子量
細(xì)胞定位 細(xì)胞核 細(xì)胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GLE1: 611-698/698 
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 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.

SWISS:
Q53GS7

Gene ID:
2733

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



產(chǎn)品圖片
Paraformaldehyde-fixed, paraffin embedded (rat testis); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (GLE1) Polyclonal Antibody, Unconjugated (bs-13371R) at 1:5000 overnight at 4°C, followed by a conjugated secondary (sp-0023) for 20 minutes and DAB staining.
版權(quán)所有 2004-2026 m.nmgps.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
一级特黄aa大片欧美 | www.四虎影视中文字幕 | 亚洲一区二区三区乱码在线观看 | 五十路人妻在线视频 | 素人美女被操到高潮完整版在线观看 | av免费在线观看免费在线观看 | 久久免费精品视频 | 亚洲色偷精品一区二区三区 | 国产伦精品一区二区三区妓女下载 | 丁香五月激情视频 | 国产三级片在线观看视频 | 波多野结衣免费观看靠比网站 | 成熟女人毛片WWW免费版在线 | 少妇无码一区二区三区免费 | 一级毛片全部免费播放特黄 | 久久精品99久久久久久 | 91在线无码精品秘 传媒 | 欧美一级婬片A片免费播放绣春 | 亚洲黄片无码在线观看 | 无码动漫3D纯肉一区二区三区 | 国产成人一区二区三区影院爱豆 | 蜜桃视频在线观看免费 | 一区二区三区四区在线 | 国产人妻精品一区二区三水牛影视 | 一区二区三区四区在线视频 | 久久人妻少妇嫩草AV蜜桃漫画 | 日韩欧美在线视频观看 | A片夜夜爽爽AAAAA片 | 一级A片在线免费观看 | 国产大学生一级A片 | 伦伦影院午夜理论片痴汉 | 17c国产精品88888 | 国产美女无遮挡在线观看 | 1000部毛片A片免费视频 | 做爰特黄AAAAAAA片 | 在线亚洲无码高清视频 | 久久AV红桃秘 一区二区 | 免费观看BBB毛片大全 | 国内精品国产成人国产三级 | 粉嫩AV一区二区夜夜嗨 | 波多野结衣A片在线观看 |