艳妇乳肉豪妇荡乳AV无码福利,最新久久国产亚洲高清观看,91久久无码99精品高潮久,中文乱码字字幕在线第5页一,免费大片av手机看片不卡高清,91精品国产91久久久久久青草_精品国产亚洲人成在线观看_91国在线啪精品一区_国产一区二区三区在线免费_国产精品v欧美精品∨日韩_日韩欧美国产三级_国产三级精品三级在专区_国产精选第一页_欧美国产精品va在线观看 ,中文字幕一区二区三区精华液_亚洲欧美一区二区视频_麻花豆剧国产MV在视频_红桃AV一区二区三区在线无码AV ,国产欧美日本亚洲精品一5|99视频在线精品国自产拍亚瑟|国产色精品vr一区区三区|国产精品极品美女自在线观看免费|欧洲精品精美色视频在线观看

最近搜索:細(xì)胞培養(yǎng) 微生物學(xué) 分子生物 生物化學(xué)
首頁(yè)>>免疫學(xué)>>一抗>>絲裂原活化蛋白激酶激酶2單克隆抗體
絲裂原活化蛋白激酶激酶2單克隆抗體
  • 產(chǎn)品貨號(hào):
    BN42021M
  • 中文名稱:
    絲裂原活化蛋白激酶激酶2單克隆抗體
  • 英文名稱:
    Mouse anti-MEK2 Monoclonal antibody
  • 品牌:
    Biorigin
  • 貨號(hào)

    產(chǎn)品規(guī)格

    售價(jià)

    備注

  • BN42021M-50ul

    50ul

    ¥1486.00

    交叉反應(yīng):Human,Mouse,Rat 推薦應(yīng)用:WB,IHC-P,IHC-F,ICC,IF

  • BN42021M-100ul

    100ul

    ¥2360.00

    交叉反應(yīng):Human,Mouse,Rat 推薦應(yīng)用:WB,IHC-P,IHC-F,ICC,IF

產(chǎn)品描述

英文名稱MEK2
中文名稱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.  
研究領(lǐng)域腫瘤  細(xì)胞生物  免疫學(xué)  神經(jīng)生物學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  激酶和磷酸酶  
抗體來(lái)源Mouse
克隆類型Monoclonal
克 隆 號(hào)4C3
交叉反應(yīng)Human, Mouse, Rat, 
產(chǎn)品應(yīng)用WB=1:1000-2000 IHC-P=1:200-1000 IHC-F=1:200-1000 ICC=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復(fù))
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量46kDa
細(xì)胞定位細(xì)胞漿 
性    狀Liquid
濃    度1mg/ml
免 疫 原Recombinant human MEK2 Protein:1-171/400 
亞    型IgG
純化方法affinity purified by Protein G
儲(chǔ) 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMedPubMed
產(chǎn)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. 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.

SWISS:
P36507

Gene ID:
5605

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(hào)轉(zhuǎn)導(dǎo)途徑中的重要成員。


灌云县| 板桥市| 句容市| 休宁县| 尼玛县| 哈尔滨市| 天全县| 屯门区| 肇东市| 西林县| 平凉市| 尚义县| 望都县| 西宁市| 当雄县| 龙井市| 娄底市| 金山区| 台湾省| 静海县| 衡东县| 来安县| 永济市| 高雄市| 德庆县| 呼玛县| 中山市| 嘉义市| 肇源县| 林州市| 交口县| 祁东县| 织金县| 唐山市| 阜新市| 廉江市| 剑河县| 错那县| 玉树县| 呼和浩特市| 凤凰县|