- ¥2980
- LMAI Bio
- LM-5503R-FITC
- 中国/美国/欧洲
- 2025年07月14日
- IF=1:50-200
- Human, Mouse, Rat, Chicken, Pig, Cow, Rabbit,
- Human, Mouse, Rat, Chicken, Pig, Cow, Rabbit,
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- 详细信息
- 文献和实验
- 技术资料
- 供应商：
上海联迈生物工程有限公司
- 库存：
大量
- 靶点：
详见说明书
- 级别：
1
- 目录编号：
LM-5503R-FITC
- 克隆性：
多克隆
- 抗原来源：
Rabbit
- 保质期：
1年
- 抗体英文名：
Anti-Phospho-MAPKAPK2(Ser272)/FITC
- 抗体名：
Anti-Phospho-MAPKAPK2(Ser272)/FITC
- 标记物：
FITC标记
- 宿主：
Human, Mouse, Rat, Chicken, Pig, Cow, Rabbit,
- 适应物种：
Human, Mouse, Rat, Chicken, Pig, Cow, Rabbit,
- 免疫原：
详见说明书
- 亚型：
IGg
- 形态：
粉末、液体、冻干粉
- 应用范围：
IF=1:50-200
- 浓度：
1mg/ml
- 保存条件：
-20 °C
- 规格：
100ul
| 英文名称 | Anti-Phospho-MAPKAPK2(Ser272)/FITC |
| 中文名称 | FITC标记的磷酸化丝裂原活化蛋白激酶活化的蛋白激酶2抗体 |
| 别 名 | MAPKAP Kinase 2 (phospho S272); p-MAPKAP Kinase 2 (phospho S272);MAPKAPK2(phospho S272);P-MAPKAPK2(Ser272); MAP Kinase Activated Protein Kinase 2; MAPK activated protein kinase 2; MAPKAP kinase 2; MAPKAPK 2; MAPKAPK2; Mitogen Activated Protein Kinase Activated Protein Kinase 2; MAPK2_HUMAN; MK 2; MK2; MAPKAPK-2. |
| 规格价格 | 100ul/2980元 购买 大包装/询价 |
| 说 明 书 | 100ul |
| 产品类型 | 磷酸化抗体 |
| 研究领域 | 肿瘤 免疫学 信号转导 转录调节因子 激酶和磷酸酶 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, Mouse, Rat, Chicken, Pig, Cow, Rabbit, |
| 产品应用 | IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 46kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated Synthesised phosphopeptide derived from human MAPKAPK2 around the phosphorylation site of Ser272 |
| 亚 型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
| 保存条件 | 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. |
| 产品介绍 | background: MAP kinase activated protein kinase 2 (MAPKAP Kinase 2), also known as p45 hsp27 kinase, is a 45-54 kDa serine/threonine protein kinase that contains a proline rich sequence and two putative SH3 binding sites. MAPKAP Kinase 2 is activated in response to stress, IL1 and TNF, possibly catalyzed by p38/Hog dependent phosphorylation. One of the major substrates of MAPKAP Kinase 2 is hsp27, which stimulates actin polymerization in order to facilitate recovery from destruction of cytoskeleton during cellular stresses. MAPKAP2 is implicated in several disorders including ischemic brain injury and heart failure and has been shown to be important in regulating stress resistance and the production of TNF alpha. Function: Stress-activated serine/threonine-protein kinase involved in cytokines production, endocytosis, reorganization of the cytoskeleton, cell migration, cell cycle control, chromatin remodeling, DNA damage response and transcriptional regulation. Following stress, it is phosphorylated and activated by MAP kinase p38-alpha/MAPK14, leading to phosphorylation of substrates. Phosphorylates serine in the peptide sequence, Hyd-X-R-X(2)-S, where Hyd is a large hydrophobic residue. Phosphorylates ALOX5, CDC25B, CDC25C, ELAVL1, HNRNPA0, HSF1, HSP27/HSPB1, KRT18, KRT20, LIMK1, LSP1, PABPC1, PARN, PDE4A, RCSD1, RPS6KA3, TAB3 and TTP/ZFP36. Mediates phosphorylation of HSP27/HSPB1 in response to stress, leading to dissociate HSP27/HSPB1 from large small heat-shock protein (sHsps) oligomers and impair their chaperone activities and ability to protect against oxidative stress effectively. Involved in inflammatory response by regulating tumor necrosis factor (TNF) and IL6 production post-transcriptionally: acts by phosphorylating AU-rich elements (AREs)-binding proteins ELAVL1, HNRNPA0, PABPC1 and TTP/ZFP36, leading to regulate the stability and translation of TNF and IL6 mRNAs. Phosphorylation of TTP/ZFP36, a major post-transcriptional regulator of TNF, promotes its binding to 14-3-3 proteins and reduces its ARE mRNA affinity leading to inhibition of dependent degradation of ARE-containing transcript. Also involved in late G2/M checkpoint following DNA damage through a process of post-transcriptional mRNA stabilization: following DNA damage, relocalizes from nucleus to cytoplasm and phosphorylates HNRNPA0 and PARN, leading to stabilize GADD45A mRNA. Involved in toll-like receptor signaling pathway (TLR) in dendritic cells: required for acute TLR-induced macropinocytosis by phosphorylating and activating RPS6KA3. Subunit: Heterodimer with p38-alpha/MAPK14. The heterodimer with p38-alpha/MAPK14 forms a stable complex: molecules are positioned 'face to face' so that the ATP-binding sites of both kinases are at the heterodimer interface. Interacts with PHC2. Subcellular Location: Cytoplasm. Nucleus. Note=Phosphorylation and subsequent activation releases the autoinhibitory helix, resulting in the export from the nucleus into the cytoplasm. Tissue Specificity: Expressed in all tissues examined. Post-translational modifications: Sumoylation inhibits the protein kinase activity. Phosphorylated and activated by MAP kinase p38-alpha/MAPK14 at Thr-222, Ser-272 and Thr-334. Similarity: Belongs to the protein kinase superfamily. CAMK Ser/Thr protein kinase family. Contains 1 protein kinase domain. Database links: Entrez Gene: 9261 Human Entrez Gene: 17164 Mouse Entrez Gene: 289014 Rat Omim: 602006 Human SwissProt: P49137 Human SwissProt: P49138 Mouse Unigene: 643566 Human Unigene: 713747 Human Unigene: 221235 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
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文献和实验的信号分 子 小分子物质，有助于信号向胞内进行传递，比如环磷腺苷 cAMP，环磷鸟苷 cGMP，以及钙离子等等，主要的作用就是活化蛋白激酶。常见信号通路总结1. NF-κB signaling pathwayNF-κB 通路作用机制当处于激活状态时，NF-κB 位于细胞质中且与抑制蛋白 IκBα 形成复合体。通过内在膜受体的介导，一些胞外信号物质可激活一种称为 IκB 激酶（IKK）的酶。IKK 转而磷酸化 IκBα 蛋白，这将导致后者的泛素化，使得 IκBα 从 NF-κB 上脱离下来，最终
蛋白激酶和蛋白磷酸酶 信号转导中信号蛋白的磷酸化和脱磷酸化十分重要，分别由蛋白激酶和磷酸酶促成。蛋白质分子上能够发生磷酸化的氨基酸残基主要有两类：酪氨酸以及丝氨酸和苏氨酸。通常，能使酪氨酸残基发生磷酸化的蛋白酪氨酸激酶(PTK)，在信号转导的上游发挥作用；而引起丝、苏氨酸磷酸化的激酶，如丝裂原活化蛋白激酶(MAPK)，较多地在信号转导的下游发挥作用，直接参与转录因子的活化。 参与T细胞激活的主要蛋白激酶和蛋白磷酸酶
质芯片检测。此外，肽芯片或基于质谱的方法[ 20，21] 也可以用于这方面。 我们在此介绍基于蛋白质芯片技术的蛋白磷酸化筛选方法和高通量确定蛋白激酶底物的方法。我们已成功地用这种筛选工具鉴定大麦酪蛋白激酶 2α ( CK 2α) 和不同的拟南芥丝裂原活化蛋白（MAP) 激酶 [23] 的新靶标。我们这个方法使用本书第 28 章详细描述的植物蛋白质芯片（见第 28 章）。在放射性【 γ33 磷】三磷酸腺苷存在的条件下，用可溶和具有活性的激酶孵育芯片。通过磷屏成像仪或 X 射线胶片检测到的放射性信号，对可能
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