產(chǎn)品編號(hào) | bs-17012R |
英文名稱 | ACTC1 Rabbit pAb |
中文名稱 | 肌動(dòng)蛋白C1抗體 |
別 名 | ACTC; ACTC_HUMAN; Actin alpha cardiac muscle 1; Actin; alpha-cardiac actin; ASD5; CMD1R; CMH11; LVNC4; Actin, alpha cardiac muscle 1; actin, alpha cardiac muscle 1 proprotein; alpha cardiac actin. |
研究領(lǐng)域 | 心血管 信號(hào)轉(zhuǎn)導(dǎo) 細(xì)胞骨架 |
抗體來(lái)源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | Human (predicted: Mouse,Rat,Rabbit,Pig,Sheep,Cow,Chicken,Dog,GuineaPig,Horse,Danio rerio) |
產(chǎn)品應(yīng)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 | 42 kDa |
檢測(cè)分子量 | |
細(xì)胞定位 | 細(xì)胞漿 |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human ACTC1: 1-50/377 |
亞 型 | IgG |
純化方法 | affinity purified by Protein A |
緩 沖 液 | Preservative: 0.02% Proclin300, Constituents: 1% BSA, 0.01M PBS, pH7.4. |
保存條件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
注意事項(xiàng) | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
PubMed | PubMed |
產(chǎn)品介紹 |
Actins are highly conserved proteins that are involved in various types of cell motility. Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to four others. The protein encoded by this gene belongs to the actin family which is comprised of three main groups of actin isoforms, alpha, beta, and gamma. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. Defects in this gene have been associated with idiopathic dilated cardiomyopathy (IDC) and familial hypertrophic cardiomyopathy (FHC). [provided by RefSeq, Jul 2008]. Function: Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. Subunit: Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to 4 others. Subcellular Location: Cytoplasm, cytoskeleton. Post-translational modifications: Oxidation of Met-46 and Met-49 by MICALs (MICAL1, MICAL2 or MICAL3) to form methionine sulfoxide promotes actin filament depolymerization. MICAL1 and MICAL2 produce the (R)-S-oxide form. The (R)-S-oxide form is reverted by MSRB1 and MSRB2, which promote actin repolymerization (By similarity). {ECO:0000250}. Monomethylation at Lys-86 (K84me1) regulates actin-myosin interaction and actomyosin-dependent processes. Demethylation by ALKBH4 is required for maintaining actomyosin dynamics supporting normal cleavage furrow ingression during cytokinesis and cell migration. DISEASE: Cardiomyopathy, dilated 1R (CMD1R) [MIM:613424]: A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. {ECO:0000269|PubMed:9563954}. Note=The disease is caused by mutations affecting the gene represented in this entry. Cardiomyopathy, familial hypertrophic 11 (CMH11) [MIM:612098]: A hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death. Note=The disease is caused by mutations affecting the gene represented in this entry. Atrial septal defect 5 (ASD5) [MIM:612794]: A congenital heart malformation characterized by incomplete closure of the wall between the atria resulting in blood flow from the left to the right atria. {ECO:0000269|PubMed:17947298}. Note=The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the actin family. SWISS: P68032 Gene ID: 70 Database links: Entrez Gene: 70 Human Entrez Gene: 11464 Mouse Omim: 102540 Human SwissProt: P68032 Human SwissProt: P68033 Mouse Unigene: 118127 Human Unigene: 686 Mouse Unigene: 3114 Rat |
產(chǎn)品圖片 | |
| 中文字字幕在线中文乱码修改方法 | 日本精品中文字幕人妻 | 91精品人妻互换一区二区 | 99精品少妇免费一区二区刘豆豆 | 三人成全免费观看电视剧高清一共多少集啊 | 欧美精品人妻无码一区久爱 | 无码三级午夜久久人妻 | 91成人一区二区 | 无码人妻一区二区三区免费九色 | 国产国语对白又又粗又大又爽 | av资源库中文在线播放 | 温泉近親入浴相姦中文 | 国产一区二区三区四区在线观看 | 窝窝人体色WWW聚色窝 | 西西444www无码精品 | 国模精品无码一区二区免费蜜桃 | 免费在线播放黄色视频 | 99人妻少妇无码αⅤ二区下载 | 国产亚无精久久久久久无码 | 国产又粗又猛又黄又爽无遮挡 | 国产精品视频在线观看 | 亚洲天堂无码在线观看 | 国产一区二区在线视频 | 成人免费观看的毛片A片 | 红桃视频hp60.vip | 国产高潮的无套A片激情视频大全 | 啊轻点灬太粗太长国产 | 欧美一级A片久久久 | 西西西444www无码视 | 精品大屁股人妻白浆 | 激情放荡性小说在线视频xx | 亚洲嫩模视频免费观看 | 国产乱人偷精品人妻A片 | 国产精品视频一区99 | 欧美 偷拍 另类 综合 | 日本中文字幕电影 | 免费无码国产v片在线观看视频 | 欧美成人性做爰高清网站 | 搡老女人老熟妇AAA黑 | 无码区免费看一级毛片A片 影音先锋中文字幕在线观看 |