CAOPORN成人免费公开,欧美FREESEX黑人又粗又大 ,欧美狠狠入鲁的视频777色,主仆调教SM束缚绳索捆绑

掃碼關(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
日本三级片在线观看,最近中文字幕免费MV视频7
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-Synphilin-1/Cy3 Conjugated antibody (bs-1905R-Cy3)
訂購熱線:400-901-9800
訂購郵箱:sales@www.tjshangbang.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@www.tjshangbang.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-1905R-Cy3
英文名稱 Rabbit Anti-Synphilin-1/Cy3 Conjugated antibody
中文名稱 Cy3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(lǐng)域 細胞生物  免疫學  神經(jīng)生物學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, Guinea Pig, )
產(chǎn)品應(yīng)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(chǎn)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(quán)所有 2004-2026 www.www.tjshangbang.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)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(zhì)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(wǎng)安備110107000727號
中国女人内射6XXXXX| GOGOGO高清免费完整版| 国产裸拍裸体视频在线观看| 国产精品毛片无码| 国产精品一久久香蕉国产线看| 熟女丝袜潮喷内裤视频网站| 青青草原综合久久大伊人精品| 亚洲 欧美 日韩综合| 精品视频一区二区三区在线观看| 欧美国产亚洲日韩在线二区| 老公不在的下午美好时光电视剧| 嗯快点别停舒服好爽受不了了| 人妻无码一区二区三区四区| 最新日本一区久爱精品免费| 把腿张开老子臊烂你| 男男无遮挡H肉真人在线观看| 免费国产高清在线精品一区| 亚洲精品无码成人片久久不卡| 亚洲色偷偷综合亚洲AVYP| 久久精品道一区二区三区| 国产精品久久久久久亚洲影视| 欧美日韩视频一区三区二区| 欧美久久天天综合香蕉伊| 亚洲AV无码一区二区三区网址| 欧美日韩一区二区三区久久| 18禁裸男晨勃露J毛免费观看| 久久99精品久久久久久婷婷| 免费男人下部进女人下部视频| 金瓶风月在线观看| 日产精品久久久久久久| 中文字幕视频一区| 国产精品精品久久久久| 日韩欧美精品一中文字幕| 龚玥菲版新梅瓶未删减| 亚洲成人色区| 天堂中文最新版在线中文| 阿公抱着我边摸边吃奶视频| 公的大龟慢慢挺进我的体内视频| 国产又黄又大又粗的视频| 日韩精品观看| 国产精品亚洲欧美一区二区|