產(chǎn)品編號 | bs-13371R-PE-Cy5 |
英文名稱 | Rabbit Anti-GLE1/PE-Cy5 Conjugated antibody |
中文名稱 | PE-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 |
研究領域 | 染色質和核信號 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 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 | |
| 无码人妻一区二区三 | 久久久久久久久久一区二区三区 | 国产精品ThePorn | caoporn视频 | 91在线无码精品秘 竹菊 | 成人短视频在线观看免费 | 国产一级婬片AAAAA片口述 | 国产成人精品免费视频 | 麻豆网站少妇AAA片 国产一区视频在线播放 | www.四虎影视中文字幕 | 中文字幕曰本髙清无码 | 26uuu精品一区二区三区 | 白丝喷白浆一区二区在线观看 | 无码做爰内谢免费视频 | 少妇摸BBBB自慰 | 国产免费观看秘 福利姬 | 日本成人在线观看网址 | 未满十八18禁止免费无码网站 | 2019高清无码视频 | 91精品久久久无码人妻 | 中文字幕无码在线视频 | 波多野结衣一级片 | 五十路老熟妇一区二区三区 | 亚洲AV无码乱码精品国产竹菊 | 国产成人无码视频 | 少妇又爽又大又黄蜜桃 | 无套内谢寡妇毛片A片 | 亚洲AV秘 无码一区田中 | 国产精品海角社区视频 | 无码秘 人妻一区二区三区 精品秘 无码一区二区久久 | 做爰高潮A片免费看视频 | 最近最经典中文MV字幕 | 欧美三级成人视频播放 | 成人网站在线播放 | 乱码丰满人妻一二三区痴汉电车 | 黄片网站免费观看视频 | 国产精品久久久久久久午夜 | 野外做受又硬又粗又大视频哈 | 亚洲日韩精品无码AV | 人妻边打电话边被躁91 |