来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

掃碼關(guān)注公眾號(hào)           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  人才招聘  關(guān)于我們  聯(lián)系我們
两女女百合互慰AV赤裸无遮挡|国产免费一区二区三区免费视频 |将军与娇妻各种做高H
Rabbit Anti-PCNT/BF488 Conjugated antibody (bs-7711R-BF488)
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@73327.net
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-7711R-BF488
英文名稱1 Rabbit Anti-PCNT/BF488 Conjugated antibody
中文名稱 BF488標(biāo)記的中心粒周蛋白抗體
別    名 Centrosome Marker; Ken; Kendrin; KIAA0402; MOPD2; PCN; PCNT 2; PCNT; PCNT B; PCNT1; PCNT2; PCNTB; PCTN2; Pericentrin 1; Pericentrin 1; Pericentrin 2; Pericentrin 380; Pericentrin B; SCKL4.  
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 細(xì)胞生物  細(xì)胞周期蛋白  細(xì)胞分化  
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, )
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 367kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Pericentrin
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:
The protein encoded by this gene binds to calmodulin and is expressed in the centrosome. It is an integral component of the pericentriolar material (PCM). The protein contains a series of coiled-coil domains and a highly conserved PCM targeting motif called the PACT domain near its C-terminus. The protein interacts with the microtubule nucleation component gamma-tubulin and is likely important to normal functioning of the centrosomes, cytoskeleton, and cell-cycle progression. Mutations in this gene cause Seckel syndrome-4 and microcephalic osteodysplastic primordial dwarfism type II. [provided by RefSeq, Jul 2008].

Function:
Integral component of the filamentous matrix of the centrosome involved in the initial establishment of organized microtubule arrays in both mitosis and meiosis. Plays a role, together with DISC1, in the microtubule network formation. Is an integral component of the pericentriolar material (PCM). May play an important role in preventing premature centrosome splitting during interphase by inhibiting NEK2 kinase activity at the centrosome.

Subunit:
Interacts with CHD3. Interacts with CHD4; the interaction regulates centrosome integrity (By similarity). Interacts with DISC1 and PCM1. Binds calmodulin. Interacts with CDK5RAP2; the interation is leading to centrosomal localization of PCNT and CDK5RAP2. Interacts with isoform 1 of NEK2.

Subcellular Location:
Cytoplasm; cytoskeleton; centrosome. Note: Centrosomal at all stages of the cell cycle. Remains associated with centrosomes following microtubule depolymerization. Colocalized with DISC1 at the centrosome

Tissue Specificity:
Expressed in all tissues tested, including placenta, liver, kidney and thymus.

DISEASE:
Defects in PCNT are the cause of microcephalic osteodysplastic primordial dwarfism type 2 (MOPD2) [MIM:210720]; also known as osteodysplastic primordial dwarfism type 2. Adults with this rare inherited condition have an average height of 100 centimeters and a brain size comparable to that of a 3-month-old baby, but are of near-normal intelligence.

Database links:
UniProtKB/Swiss-Prot: O95613.4

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.73327.net 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(hào): 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(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
696969大但人文艺术正道| 又污又爽又黄的网站| 又白又嫩毛又多15P| 无人视频在线观看完整版高清| 2018Av天堂在线视频精品观看| 亚洲国产婷婷香蕉久久久久久| 国产精品黄黄久久免费看| 久久gvav| 人交獸AV完整版在线观看| 久久午夜夜伦鲁鲁片无码免费| 久久无码专区国产精品S| 亚洲精品久久无码| 国产欧美熟妇另类久久久| 日韩亚洲欧美久久久| 国产精品+亚洲+欧美| 国内精品视频一区二区三区八戒| 久久久国产精华液| 国产50部艳色禁片无码| 免费人成在线观看网站| 亚洲2022国产成人精品无码区| 色五月丁香六月欧美综合| 国产97色在线 | 国产| 亚洲AV无码专区在线观看成人| 污污污网站国产精品一区| 日本αv一区二区三区| 中美日韩毛片免费观看| 婷婷五月深爱憿情网六月综合| 国产精彩视频一区二区三区| 亚洲精品国产精品国自产久久| 不用播放器的AV| 国产精品丝袜黑色高跟鞋| 一区二区三区特黄色片| 性VODAFONEWIFI另类| 久久国产精品无码网站| 男人添女人下部高潮全视频| 国产麻豆剧传媒精品国产av| 中文字幕日韩欧美一区二区三区| 午夜一区二区国产好的精华液| 国产成人涩涩涩视频在线观看| 欧美成人一级片在线观看| 国产精品成人国产乱|