產(chǎn)品編號(hào) | bs-11777R-Bio |
英文名稱 | Rabbit Anti-ZFYVE27/Biotin Conjugated antibody |
中文名稱 | 生物素標(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 購買 大包裝/詢價(jià) |
說 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 | WB=1:50-200 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 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. |
| 东北免费黄色电影网站 | 精品人妻伦一二三区久久春菊 | 中文字幕熟女人妻av一区二区三区 | 超碰在线免费成人WWW | 国产人妻人伦精品无码.麻豆 | 中文字幕一区二区人妻久久 | 少妇伦子伦5在线播放 | 蜜臀AⅤ色欲av浪潮夜夜 | 国产精人妻无码一区果冻 | 免费看的黄色AAAAA片 | 国产毛多水多女人A片色情舞 | 天天鲁一鲁摸一摸爽一爽 | 粉嫩一区二区三区粉嫩视频 | 最好看的2019中文大全在线观看 | 亚洲日韩高清无码 | 美女被操喷水视频免费看 | 人人妻人人澡人人爽电台app | 强伦人妻一区二区三区电影 | 欧美老熟妇乱大交XXXXX | 内射后入美女屁屁网站 | 日本私人一二三四区色欲 | 一区二区污污网站在线观看 | 色五月婷婷在线观看 | 少妇搡BBBB搡BBB搡澳门 | 蜜桃AV无码一区二区三区 | 亚洲一区二区五十路激情中出自拍 | 欧美激情xxxx性爱 | 国产一区二区在线免费观看 | 国产一级a毛一级a看免 | 黄色片在线观看播放用户 | 性精品 A片天美 | 免费无码婬片AAAA片直播 | 小向美奈子乳巨码在线播放 | 成人h精品动漫一区二区三区 | 亚洲精品视频免费观看 | 黄色AV污污污大片在线看自拍 | 91九色网曝门g,g视频 | 成人免费A级毛片无码片2023 | 久久人妻嫩草无码AV专区动漫 | 人妻熟女一区二区AⅤ天美 粉嫩Av绯色AV蜜乳AV |