mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

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  人才招聘  關于我們  聯系我們
亚洲黄色视频道男男,国产精品一区二区三区肉骚,中文字幕久久视频在线观看
首頁 > 產品中心 > 一抗 > 產品信息
Rabbit Anti-MEK2  antibody (bsm-63042R)  
~~~促銷代碼KT202411~~~
訂購熱線:400-901-9800
訂購郵箱:sales@m.p2b3.cn
訂購QQ:  400-901-9800
技術支持:techsupport@m.p2b3.cn
說明書: 50ul  100ul  
50ul/1580.00元
100ul/2500.00元
大包裝/詢價

產品編號 bsm-63042R
英文名稱 Rabbit Anti-MEK2  antibody
中文名稱 絲裂原活化蛋白激酶激酶2重組兔單抗
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; MP2K2_HUMAN; OTTHUMP00000165826; OTTHUMP00000165827; PRKMK 2; PRKMK2 V.  
抗體來源 Rabbit
克隆類型 Recombinant
交叉反應 Human,Mouse
產品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 46kDa
細胞定位 細胞漿 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MAPKK2 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 10mM phosphate buffered saline , pH 7.4, 150mM sodium chloride, 0.05% BSA, 0.02% sodium azide and 50% glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 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 (By similarity). Interacts with SGK1.

Subcellular Location:
Cytoplasm, cytoskeleton, centrosome. Cytoplasm, cytoskeleton, spindle pole body. Cytoplasm. Nucleus. Note=Localizes at centrosomes during prometaphase, midzone during anaphase and midbody during telophase/cytokinesis.

Tissue Specificity:
Widely expressed, with extremely low levels in brain.

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.

SWISS:
P36507

Gene ID:
407835

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



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。
產品圖片
25 ug total protein per lane of various lysates (see on figure) probed with MEK2 monoclonal antibody, unconjugated (bsm-63042R) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at r.t. for 60 min.
版權所有 2004-2026 www.m.p2b3.cn 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
九七成人操碰人人看小视频| 亚洲欧美成人久久一区二区三区| 国产好大对白露脸高潮| 国语自产拍无码精品视频在线| 国产乱老熟女乱老熟女视频| 国产精品秘久久久久久| 国产爽的冒白浆的视频| 麻豆理论片在线观看| 91午夜精品亚洲一区二区三区| 日韩特黄特刺激午夜毛片| 欧美精品在欧美一区二区三区| 国产精品久久久久国产三| 中文字幕无码aⅴ免费不卡| 日本阿v不卡在线观看视频| 午夜精品久久久久久久久久久| 白嫩丰满少妇一区二区| 一区二区三区欧美日本| 不卡在线视频一区二区| 黑人操亚洲女一级黄色片| 日本精品一线在线观看| 不卡在线视频一区二区| 亚洲永久精品国产来久精品| 国偷自产av一区二区三区| 亚洲国产精品无码久久久高潮| 久久蜜臀亚洲一区二区| 亚洲国产精品一区二区三区久久| 久久久成人国产精品麻豆| 2018在线不卡爱视频| 亚洲精中文字幕二区三区| 极品少妇欧美一区二区| 欧美日韩一区二区三区自拍| 国产av剧情亚洲精品| 欧美亚洲综合一区色婷婷| 日韩的一区二区另类免费| 国产精品日本女优在线观看| 欧美老熟女多毛茸茸| 高清国产午夜精品久久久久久| 青青草原精品国产亚洲av| 国产精品日本女优在线观看| 国产一区二区三区欧美日| 国产微拍无码精品一区|