產(chǎn)品編號 | bs-19244R-Cy3 |
英文名稱 | Rabbit Anti-CHRNE/Cy3 Conjugated antibody |
中文名稱 | Cy3標記的煙堿型乙酰膽堿受體ε抗體 |
別 名 | Nicotinic Acetylcholine Receptor epsilon; Acetylcholine receptor subunit epsilon; ACHE_HUMAN; AchR epsilon subunit; ACHRE; Cholinergic receptor, nicotinic, epsilon polypeptide; Chrne; CMS1D; CMS1E; CMS2A; FCCMS; SCCMS. |
規(guī)格價格 | 100ul/2980元 購買 大包裝/詢價 |
說 明 書 | 100ul |
研究領域 | 細胞生物 神經(jīng)生物學 細胞膜受體 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應 | (predicted: Human, Mouse, Rat, ) |
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 | 53kDa |
性 狀 | Lyophilized or Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human CHRNE |
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: Acetylcholine receptors at mature mammalian neuromuscular junctions are pentameric protein complexes composed of four subunits in the ratio of two alpha subunits to one beta, one epsilon, and one delta subunit. The acetylcholine receptor changes subunit composition shortly after birth when the epsilon subunit replaces the gamma subunit seen in embryonic receptors. Mutations in the epsilon subunit are associated with congenital myasthenic syndrome. [provided by RefSeq, Sep 2009] Function: After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. Subunit: Pentamer of two alpha chains, and one each of the beta, delta, and gamma (in immature muscle) or epsilon (in mature muscle) chains. Subcellular Location: Cell junction; synapse; postsynaptic cell membrane. Cell membrane. DISEASE: Note=The muscle AChR is the major target antigen in the autoimmune disease myasthenia gravis. Myasthenia gravis is characterized by sporadic muscular fatigability and weakness, occurring chiefly in muscles innervated by cranial nerves, and characteristically improved by cholinesterase-inhibiting drugs. Defects in CHRNE are a cause of congenital myasthenic syndrome slow-channel type (SCCMS) [MIM:601462]. SCCMS is the most common congenital myasthenic syndrome. Congenital myasthenic syndromes are characterized by muscle weakness affecting the axial and limb muscles (with hypotonia in early-onset forms), the ocular muscles (leading to ptosis and ophthalmoplegia), and the facial and bulbar musculature (affecting sucking and swallowing, and leading to dysphonia). The symptoms fluctuate and worsen with physical effort. SCCMS is caused by kinetic abnormalities of the AChR, resulting in prolonged endplate currents and prolonged AChR channel opening episodes. Defects in CHRNE are a cause of congenital myasthenic syndrome fast-channel type (FCCMS) [MIM:608930]. FCCMS is a congenital myasthenic syndrome characterized by kinetic abnormalities of the AChR. In most cases, FCCMS is due to mutations that decrease activity of the AChR by slowing the rate of opening of the receptor channel, speeding the rate of closure of the channel, or decreasing the number of openings of the channel during ACh occupancy. The result is failure to achieve threshold depolarization of the endplate and consequent failure to fire an action potential. Defects in CHRNE are a cause of congenital myasthenic syndrome with acetylcholine receptor deficiency (CMS-ACHRD) [MIM:608931]. CMS-ACHRD is a postsynaptic congenital myasthenic syndrome. Mutations underlying AChR deficiency cause a 'loss of function' and show recessive inheritance. Similarity: Belongs to the ligand-gated ion channel (TC 1.A.9) family. Acetylcholine receptor (TC 1.A.9.1) subfamily. Epsilon/CHRNE sub-subfamily. Database links: Entrez Gene: 1145 Human Entrez Gene: 101137825 Gorilla Entrez Gene: 100146223 Horse Entrez Gene: 11448 Mouse Entrez Gene: 710301 Rhesus monkey GenBank: NP_033733.1 Mouse Omim: 100725 Human SwissProt: Q04844 Human SwissProt: P20782 Mouse Unigene: 654535 Human Unigene: 4980 Mouse Unigene: 10301 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 | |
| 国产黃色A片三級三級三級四川 | 成人h动漫精品一区二区 | 绝色丰满少妇无码A片 | 7777色情网黄A片免费看蜜臀 | 69人妻人人澡人人爽人人精品 | 搡BBBB搡BBB搡我瞎了 | 台湾少妇搡BBBB搡BBBB | 91无码人妻一区二区 | 91精品国产乱码久久久 | 国产AⅤ无码一区二区 | 成人午夜福利在线观看 | 公车被奷到高潮很舒服在线观看 | 无码人妻aV一区二区三区色欲 | 懂色一区二区三区久久久 | 搡老外BBBB搡BBBB | 欧美成人r级一级二级三级 国产人妻互换一级毛片日本 | 人人色超碰阁在线 | 欧美性A片久久一级毛片欲海记 | 国产欧美精品一区二区 | 日本AⅤ毛片无码 9 2 1 5蜜桃 | 波多野结衣毛片在线观看 | 掀开奶罩边躁狠狠躁喷白浆 | 黄色成年美女网站性 XX | 五十老熟妇乱子伦免费章节 | 美女喷水网站乱伦 | 亚洲精品字幕在线观看 | 一级婬片A片免费播放桃色 国产综合一区二区教师AV | 免费一级婬A片久久久爽死你网站 | 男人日女人视频免费 | 成年人免费在线视频 | 少妇BBBB搡BBBB搡BBBB | 四川妇搡BBBBB搡BBB | 无码区免费看一级毛片A片 中文字幕日产A片在线看 | 波多野结衣高潮狂喷hd | 国产日韩精品无码去免费专区国产 | 久久综合久色欧美综合狠狠 | 人妻洗澡被强公日日视频无码动漫 | 蜜桃精品在线观看免费 | 最好看的2019中文大全在线观看 | 亚洲熟妇无码aV在线观看网址 |