精品国产av自拍_精品日韩欧美在线视频一区二区_一区二区在线观看在线_福利在线观看免费高清完整版_无码免费动漫老黄网站_无码一区在线观看视频_精品五月精品婷婷_免费国产日本高清_亚洲特黄特色一级在线观看_国产Ⅴ亚洲Ⅴ欧美Ⅴ专区

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(zhì)量反饋  關于我們  聯(lián)系我們
午夜精品久久久内射近拍高清 ,人人妻人人爽人人澡欧美二区,91亚洲精品无码久久久久
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Mouse Anti-MEK2/RBITC Conjugated antibody (bsm-33216M-RBITC)
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(chǎn)品編號 bsm-33216M-RBITC
英文名稱 Mouse Anti-MEK2/RBITC Conjugated antibody
中文名稱 羅丹明(RBITC)標記的絲裂原活化蛋白激酶激酶2單克隆抗體
別    名 Cardiofaciocutaneous syndrome; CFC syndrome; Dual specificity mitogen activated protein kinase kinase 2; Dual specificity mitogen-activated protein kinase kinase 2; ERK activator kinase 2; FLJ26075; MAP kinase kinase 2; MAP2K 2; map2k2; MAPK / ERK kinase 2; MAPK/ERK kinase 2; MAPKK 2; MAPKK2; MEK 2; MEK2; Microtubule Associated Protein Kinase Kinase 2; Mitogen activated protein kinase kinase 2; Mitogen activated protein kinase kinase 2 p45; MKK 2; MKK2; MP2K2_HUMAN; OTTHUMP00000165826; OTTHUMP00000165827; PRKMK 2; PRKMK2 V.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  免疫學  神經(jīng)生物學  信號轉導  激酶和磷酸酶  
抗體來源 Mouse
克隆類型 Monoclonal
克 隆 號 4C3
交叉反應 Human, Mouse, Rat, 
產(chǎn)品應用
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 Recombinant human MEK2 Protein
亞    型 IgG
純化方法 affinity purified by Protein G
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:
The protein encoded by this gene is a dual specificity protein kinase that belongs to the MAP kinase kinase family. This kinase is known to play a critical role in mitogen growth factor signal transduction. It phosphorylates and thus activates MAPK1/ERK2 and MAPK2/ERK3. The activation of this kinase itself is dependent on the Ser/Thr phosphorylation by MAP kinase kinase kinases. Mutations in this gene cause cardiofaciocutaneous syndrome (CFC syndrome), a disease characterized by heart defects, mental retardation, and distinctive facial features similar to those found in Noonan syndrome. The inhibition or degradation of this kinase is also found to be involved in the pathogenesis of Yersinia and anthrax. A pseudogene, which is located on chromosome 7, has been identified for this gene. [provided by RefSeq, Jul 2008].

Function:
Catalyzes the concomitant phosphorylation of a threonine and a tyrosine residue in a Thr-Glu-Tyr sequence located in MAP kinases. Activates the ERK1 and ERK2 MAP kinases.

Subunit:
Interacts with MORG1. Interacts with SGK1.

Post-translational modifications:
MAPKK is itself dependent on Ser/Thr phosphorylation for activity catalyzed by MAP kinase kinase kinases (RAF or MEKK1). Phosphorylated by MAP2K1/MEK1.
Acetylation of Ser-222 and Ser-226 by Yersinia yopJ prevents phosphorylation and activation, thus blocking the MAPK signaling pathway.

DISEASE:
Defects in MAP2K2 are a cause of cardiofaciocutaneous syndrome (CFC syndrome) [MIM:115150]; also known as cardio-facio-cutaneous syndrome. CFC syndrome is characterized by a distinctive facial appearance, heart defects and mental retardation. Heart defects include pulmonic stenosis, atrial septal defects and hypertrophic cardiomyopathy. Some affected individuals present with ectodermal abnormalities such as sparse, friable hair, hyperkeratotic skin lesions and a generalized ichthyosis-like condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitemporal constriction, hypoplastic supraorbital ridges, downslanting palpebral fissures, a depressed nasal bridge, and posteriorly angulated ears with prominent helices. The inheritance of CFC syndrome is autosomal dominant.

Similarity:
Belongs to the protein kinase superfamily. STE Ser/Thr protein kinase family. MAP kinase kinase subfamily.
Contains 1 protein kinase domain.

Database links:

Entrez Gene: 407835 Human

Entrez Gene: 5605 Human

Entrez Gene: 26396 Mouse

Entrez Gene: 58960 Rat

Omim: 601263 Human

SwissProt: P36507 Human

SwissProt: Q63932 Mouse

SwissProt: P36506 Rat

Unigene: 465627 Human

Unigene: 275436 Mouse

Unigene: 82693 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

絲裂原活化蛋白激酶激酶(MAPKK)是信號轉導途徑中的重要成員。
版權所有 2004-2026 0592123.cn 北京博奧森生物技術有限公司
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
亚洲国产成人久久综合一区77 | 国产精品欧美日韩一区二区三区在线 | 亚洲综合无码一区二区三区加勒比 | 熟妇丰满大屁股在线播放BBW | 国产精品久久久久永久免费看 | 国产精品毛片久久久久久久 | 又污又黄又无遮挡的网站国产 | 无码人妻免费—区二区三 | 日本肉体XXXX裸体137大胆图 | 日本成本人片高清久久免费 | 国产又爽又黄无码无遮挡在线观点 | 人妻久久相姦中文字幕 | 亚洲AV鲁丝一区二区三区 | 亚洲一区爱区精品无码 | 欧美中文字幕一区二区三区 | 中文精品一区二区三区四区 | 国产AV麻豆mag剧集 | 2020国产欧洲精品视频 | 国产精品毛片a∨一区二区三区 | japanese乱人伦精品 | 久久久国产精品免费看 | 性一交一乱一色一免费无遮挡 | 国产99视频精品免费视亚洲一级Av无码毛片久久精品 | 免费看成人AA片无码视频吃奶 | 日本成A人片在线观看网站 开心久久婷婷综合中文字幕 | 性成熟黑人双插美国1819 | 97在线视频免费人妻 | 国产第一页浮力影院草草 | 国产精品视频免费视频 | 18禁止看的免费污网站 | 日本DVD专区中文在线 | 亚洲国产精品久久久久秋霞影院 | 风情艳主调教朋友圈变态 | 国产真实乱子伦精品视频 | 18禁美女黄网站色大片免费看 | 亚洲免费在线播放 | 好好的曰com久久 | 日韩在线视频一区二区三区 | 无码中文字幕日韩专区 | 国模沟沟一区二区三区 | 国产精品高潮视亚洲乱码 |