91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯(lián)系我們
免费观看全黄做爰的视频,国产婬片lA片www777,四川少妇BBB搡BBB爽爽爽视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Synphilin-1/BF555 Conjugated antibody (bs-1905R-BF555)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-1905R-BF555
英文名稱 Rabbit Anti-Synphilin-1/BF555 Conjugated antibody
中文名稱 BF555標記的核突觸蛋白相互作用蛋白1抗體
別    名 Synphilin-1; Synphilin1; Synphilin 1; Alpha-synuclein-interacting protein; Sncaip; Syph1, Syph 1,Syph-1; Alpha synuclein interacting protein; MGC39814; SNCAIP; SNCAP_HUMAN; Sph1; Synuclein alpha interacting protein (synphilin); SYPH 1.  
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  免疫學  神經生物學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, Guinea Pig, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 100kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Synphilin-1
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:
This gene encodes a protein containing several protein-protein interaction domains, including ankyrin-like repeats, a coiled-coil domain, and an ATP/GTP-binding motif. The encoded protein interacts with alpha-synuclein in neuronal tissue and may play a role in the formation of cytoplasmic inclusions and neurodegeneration. A mutation in this gene has been associated with Parkinson's disease. Alternatively spliced transcript variants encoding different isoforms of this gene have been described, but the full-length nature of only two have been determined. [provided by RefSeq, Jul 2011].

Function:
Isoform 2 inhibits the ubiquitin ligase activity of SIAH1 and inhibits proteasomal degradation of target proteins. Isoform 2 inhibits autoubiquitination and proteasomal degradation of SIAH1, and thereby increases cellular levels of SIAH. Isoform 2 modulates SNCA monoubiquitination by SIAH1.

Subunit:
Homodimer (Probable). Heterodimer of isoform 1 and isoform 2 (Probable). Interacts with SIAH1, SIAH2, SNCA, RNF19A AND PARK2. Isoform 2 has a strong tendency to form aggregates and can sequester isoform 1.

Subcellular Location:
Cytoplasm. Detected in cytoplasmic inclusion bodies, together with SNCA.

Tissue Specificity:
Detected in brain (at protein level). Widely expressed, with highest levels in brain, heart and placenta.

Post-translational modifications:
Ubiquitinated; mediated by SIAH1, SIAH2 or RNF19A and leading to its subsequent proteasomal degradation. In the absence of proteasomal degradation, ubiquitinated SNCAIP accumulates in cytoplasmic inclusion bodies. Isoform 2 is subject to limited ubiquitination that does not lead to proteasomal degradation.

DISEASE:
Parkinson disease (PARK) [MIM:168600]: A complex neurodegenerative disorder characterized by bradykinesia, resting tremor, muscular rigidity and postural instability. Additional features are characteristic postural abnormalities, dysautonomia, dystonic cramps, and dementia. The pathology of Parkinson disease involves the loss of dopaminergic neurons in the substantia nigra and the presence of Lewy bodies (intraneuronal accumulations of aggregated proteins), in surviving neurons in various areas of the brain. The disease is progressive and usually manifests after the age of 50 years, although early-onset cases (before 50 years) are known. The majority of the cases are sporadic suggesting a multifactorial etiology based on environmental and genetic factors. However, some patients present with a positive family history for the disease. Familial forms of the disease usually begin at earlier ages and are associated with atypical clinical features. Note=Disease susceptibility may be associated with variations affecting the gene represented in this entry.

Similarity:
Contains 6 ANK repeats.

Database links:

Entrez Gene: 9627 Human

Entrez Gene: 67847 Mouse

Entrez Gene: 307309 Rat

Omim: 603779 Human

SwissProt: Q9Y6H5 Human

SwissProt: Q99ME3 Mouse

Unigene: 426463 Human

Unigene: 292168 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 m.rvdoil.com 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫(yī)療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
朝鲜揉BBB搡BBB视频 | 仙踪林免费网站入口www | 国产一区二区三区在线h | 91在线视频免费观看 | 美女裸体视频免费观看久久 | 一级a毛片免费观看久久精品 | 天天干天天日夜夜吻 | 日本成人一区二区 | 国产一级毛片一级A片酒瓶 五十老熟妇乱子伦免费章节 | 黄色视频网站在线下载观看 | 免费 无码 国产免费 | 少妇与禽性A片免费观看 | 一区二区三区日本性爱 | 91精品在线免费视频 | 色噜噜综合熟女人妻一区 | 欧美成人无码片免费看A片秀色 | 十八禁片网站在线免费观看 | 免费美女无遮挡久久久 | 粉嫩小泬无码无套在线观看 | 日韩欧美丝袜人妻自拍偷拍 | 女同久久另类69精品国产 | 国产伦精品一级A片视频夜夜 | 西西4444www无码精品 | 做暧暧视频高潮一区二区三区 | HEYZO高无码国产精品一本蓝牛 | 影音先锋亚洲资源 | 亚洲jizz无码人妻 | 国产精品999免费看 粉嫩18虎白女20P | 农村妇女躁BBBB高朝喷水电影 | 99国产揄拍国产精品 | 国产精品久久久久久亚洲色 | 国产电影中文字幕无码 | 日本一区不卡在线观看 | av在线观看高清无码 | 人妻边打电话边被躁91 | 国产精品久久久久久一级毛片许晴 | 国产又粗又猛又爽 | 午夜精品在线免费观看 | 亚洲av免费在线 | 精品视频免费观看 | 国产无码精品视频 |