產(chǎn)品編號(hào) | bs-11777R-PE-Cy5 |
英文名稱(chēng) | Rabbit Anti-ZFYVE27/PE-Cy5 Conjugated antibody |
中文名稱(chēng) | PE-Cy5標(biāo)記的鋅指FYVE結(jié)構(gòu)域蛋白27抗體 |
別 名 | Protrudin; RP11 459F3.2; SPG33; ZFY27_HUMAN; ZFYVE27; zinc finger FYVE domain containing 27; Zinc finger FYVE domain containing protein 27; Zinc finger FYVE domain-containing protein 27. |
規(guī)格價(jià)格 | 100ul/2980元 購(gòu)買(mǎi) 大包裝/詢(xún)價(jià) |
說(shuō) 明 書(shū) | 100ul |
研究領(lǐng)域 | 神經(jīng)生物學(xué) 鋅指蛋白 細(xì)胞膜蛋白 |
抗體來(lái)源 | Rabbit |
克隆類(lèi)型 | Polyclonal |
交叉反應(yīng) | Human, Mouse, Rat, (predicted: Dog, Cow, Rabbit, ) |
產(chǎn)品應(yīng)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 | 46kDa |
性 狀 | Lyophilized or Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human ZFYVE27 |
亞 型 | IgG |
純化方法 | affinity purified by Protein A |
儲(chǔ) 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: Zinc finger FYVE domain-containing protein 27 (ZFYVE27), also known as SPG33, is a 411 amino acid member of the FYVE-finger family of proteins. The FYVE domain is a cysteine-rich domain of about 70 amino acids that plays a role in the endosomal localization of the FYVE-finger proteins, and a majority of these proteins serve as regulators of endocytic membrane trafficking. ZFYVE27, a multi-pass membrane protein, is an endosomal protein that binds to Spastin, a protein that is primarily involved in microtubule dynamics and severing, vesicular trafficking and endosomal trafficking. Mutations in the gene encoding ZFTVE27 affect neuronal intracellular trafficking in the corticospinal tract and are thought to lead to hereditary spastic paraplegia (HSP), a neurodegenerative disorder, characterized by progressive paralysis of the legs, which is caused by impaired axonal transport. Five isoforms of ZFYVE27 exist as a result of alternative splicing events. Function: Functions as an upstream inhibitor of RAB11, regulating directional protein transport to the forming neurites. Involved in nerve growth factor-induced neurite formation. May have a more general role in cell projections formation. Subcellular Location: Recycling endosome membrane. Endoplasmic reticulum membrane. Cell projection > growth cone membrane. Cell membrane. Localizes at both dendrites and axons. Post-translational modifications: Phosphorylated. Phosphorylation is induced by NGF through the MAPK/ERK pathway and modulates interaction with RAB11A. DISEASE: Defects in ZFYVE27 are the cause of spastic paraplegia autosomal dominant type 33 (SPG33) [MIM:610244]. Spastic paraplegia is a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. Note=According to PubMed:18606302, the properties of the variant Val-191 and its frequency in some populations raise doubts on the implication of that gene in the disease. Similarity: Contains 1 FYVE-type zinc finger. Database links: Entrez Gene: 118813 Human Entrez Gene: 319740 Mouse Omim: 610243 Human SwissProt: Q5T4F4 Human SwissProt: Q3TXX3 Mouse Unigene: 523194 Human Unigene: 287359 Mouse Unigene: 470071 Mouse Unigene: 99939 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 黄色在线观看视频网站 | 中文字幕在线观看视频一区 | 国产精品无码免费在线 | 东北少妇不戴套对白第一次 | 中文字字幕中文在线 | 国产精品久久久久蜜臀 | 久久人妻嫩草无码AV专区动漫 | 蜜桃视频一区二区三区 | 黄污网站在线观看免费在线 | 国产精品久久久久久一级毛片 | 亚洲AV无码专区一级淫片毛片 | 99精品欧美一区二区三区综合在线 | 丰满又紧又爽又丰满视频 | 亚洲日韩国产中文字幕一区二区 | 国产福利在线观看 | 欧美BBw搡BBBB槡BBBB| 媚黑极品魔都绿帽人妻找黑人 | 老熟女太熟了x98AV | 茄子视频成人一区二区 | 日韩成人AV网站 | 国产一区二区三区三区在线视频观看 | 成人做爰www看视频外网 | 美女性感黄色免费网站 | 91精品国产综合久久久不卡98口 | 久久成人秘 18免费观看 | 潘金莲全黄—级A片性舒淇 亚洲午夜精品一区二区蜜桃 | 波多野结衣高清一极特黄 | 91精品少妇一区二区三区蜜桃臀 | 中文字幕永久精品国产 | 啊轻点灬太粗太长国产 | 91精品国产乱码久久久 | 一本无码人妻一区二区 | 国精品无码一区二区三区在线秋菊 | 老熟妇无码伦子伦456 | 91丨露脸丨熟女 | 韩国无码电影在线观看 | 蜜桃秘 无码一线二线三线av | 亚洲精品一区中文字幕乱码 | 午夜福利网站在线观看 | 四虎成人影视8848亚洲 |