產品編號 | bs-13371R-Cy7 |
英文名稱 | Rabbit Anti-GLE1/Cy7 Conjugated antibody |
中文名稱 | Cy7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, ) |
產品應用 |
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 | |
| 天天躁日日躁BBBBB | 九色丝袜视频自拍啪啪 | 奶好大灬好硬灬好爽在线播放 | 女无遮挡动态版120 欧美性爱一区二区三区 | 欧美成人免费在线视频 | 成人影片在线免费观看 | 高质量国产美女性爱在线观看网站 | 欧美顶级黃色大片免费 | 寡妇高潮一级毛片免费看 | 精品人妻无码一级A片 | 久久99深爱久久99精品 | 国产最爽的乱婬绿帽3p | 亚洲国产精品二二三三区 | 成人做爰高潮片免费看视频 | 人人妻人人澡人人爽少妇 | 亚洲一级av无码毛片www | 欧美成人在线视频人妻 | 少妇高潮毛片免费观看A | 男人和女人差差啊啊啊啊啊 | 睡熟迷奷系列新婚之夜 | 欧美,日韩,国产在线 | 亚洲精品无码又大又粗 | 91精品国产乱码久久 | 特级西西444WWW大精品视频 | 色欲久久久天天天综合网 | 可以免费观看的黄色视频 | 欧美色图之五月激情 | 高潮到失禁变态另类视频 | 亚洲BBBB爽爽爽自慰 | 黑人解禁久久影院 | 亚洲素人无码不卡中文字幕 | 搞A V一区二区三区 国产在线啊啊啊要射了 | 国产精品一区二区裸体美女 | 亚洲第一成人无码A片 | 性做久久久久久久久 | 五十路人妻中出息子无码 | 美女草草视频高清在线播放 | 精品无码秘 人妻一区二蜜桃 | 日本一级特黄大真人片 | 无码国产Av天堂杏 |