產(chǎn)品編號(hào) | bs-11777R-PE-Cy7 |
英文名稱 | Rabbit Anti-ZFYVE27/PE-Cy7 Conjugated antibody |
中文名稱 | PE-Cy7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 大包裝/詢價(jià) |
說(shuō) 明 書 | 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. |
| 无遮挡高潮视频在线观看 | 日韩互交免费网址 | 亚洲无码中文字幕在线观看 | 日韩AV免费在线观看 | 免费一级婬片A片AAA毛片肥女 | 国产污污视频在线观看 | 欧美精品人妻无码一区久爱 | 特级西西4444WWW无码 | 亚洲精品又大又黄又爽又长 | 亚洲综合熟女久久久30p蜜臀 | 无码国产69精品久久久久同性 | 巨大乳人妻中文字幕 | 91在无码线精品秘 入口九色 | 无码人妻精品一区二区蜜桃在 | 天天影视网天天综合色在线播放 | 国产精品成人国产乱一区 | 四川BBB搡BBB爽爽爽欧美 | 少妇高潮喷水尖叫抽搐 | 国产又粗又猛又爽 | 美女裸体视频免费观看久久 | 极品人妻无人夸337p | 国产熟妇精品AAAAA | 内射中出日韩无国产剧情 | 日本成熟人妻理伦无码新片 | 人妻体内谢精无码视频 | 亚洲小说欧美激情另类A片小说 | 91蜜桃传媒精品久久久一区二区 | 国产黑料网爆AV在线 | 少女哔哩哔哩免费观看视频 | 色五月色婷婷开心五月 | 51国产熟妇无码精品 | 波多野结衣一二三区 | 17c人妻无码一区二区三区 | 国产一级a毛一级a看免费人娇 | 麻豆传媒国产特级无码毛片 | 国产成人一区二区红桃解说 | 午夜视频网站在线观看 | 日韩成人AV一区二区 | 久久久久无码精品 | 17c成人免费视频在线观看 |