產(chǎn)品編號 | bs-13371R-Cy5 |
英文名稱 | Rabbit Anti-GLE1/Cy5 Conjugated antibody |
中文名稱 | Cy5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(lǐng)域 | 染色質(zhì)和核信號 信號轉(zhuǎn)導 轉(zhuǎn)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 GenBank: BC030012 Human Omim: 603371 Human SwissProt: Q53GS7 Human SwissProt: Q8R322 Mouse 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. |
1、抗體溶解方法 | |
2、抗體修復方式 | |
3、常用試劑的配制 | |
4、免疫組化操作步驟 | |
5、免疫組化問題解答 | |
6、Western Blotting 操作步驟 | |
7、Western Blotting 問題解答 | |
8、關(guān)于肽鏈的設計 | |
9、多肽的溶解與保存 | |
10、酶標抗體效價測定程序 | |
| 久久久久久91香蕉国产夜本色 | 成人天码区免费A片 | 99精品国产免费久久久久久下载 | 少妇又紧又色又爽又刺激视频 | 少妇搡BBBB搡BBB搡澳门 | 亚洲精品一区二区三区在线 | 亚洲国产精品国自产拍AⅤ 国产成人无码一区二区三区 | 91在线无码秘 入口在线 | 免费婬乱AAA大片 - 百度 | 国产一级先免费观看 | 红桃视频在线观看免费一区二区三区 | 久久午夜精品人妻一区二区三区 | 亚洲精品无码一区二区多久 | 蜜桃一区二区在线视频 | 美女脱光黄色裸体网站 | 常州熟女自慰-91Porn | 国产农村乱婬片A片AAA图片 | 国产91国精产品官网 | 人人妻人人澡人人爽人人 | 无高清人妻一区二区 | 亚洲综合综合精品综合 | 国产精品高潮呻吟无码AV | 欧美丰满少妇东北少妇 | 欧美一级婬片A片免费播放绣春 | 欧洲无码A片人妻久尤物伊曼纽尔 | 国内精品成人AV | 2019中文在线高清观看电视剧 | 搡BBB摸BBB摸BBBwww | 四川BBB搡BBB搡多人刮 | 东北女人无套内谢毛片 | 91黑料反差婊在线观看 | 四房色不卡免费视频在线观看 | 国产又黄又爽的免费视频 | 中文无码日本一级A片人 | 安徽妇搡BBBB搡BBBB视频 | 17c.com少妇喷水| 一区二区污污网站在线观看 | 四川BBB搡BBBB视频 | 韩国无码一区二区三区 | 国产又爽又黄无码无遮在线观看 |